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+++ b/tools/actions/convert/test/fixtures/blog3-converted.html
@@ -1,4 +1,3 @@
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 <body>
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@@ -9,15 +8,24 @@
           <div>
             <ul>
               <li><a href="/us/en/blog.html">Blog</a></li>
-              <li><a href="/us/en/blog/enabling-science-at-scale.html">Enabling Science at Scale</a></li>
+              <li><a href="/us/en/blog/enabling-science-at-scale.html">Scaling Science</a></li>
             </ul>
           </div>
         </div>
       </div>
       <hr>
       <h1>Enabling Science at Scale: How Danaher Life Sciences partners deep with Biopharma</h1>
-      <p><a href="https://player.vimeo.com/video/842870177">Video Player</a></p>
-      <p>The demand for advanced therapeutics and new drug modalities is expected to explode in the coming decade. For example, more than 2,000 gene therapies and modified cell therapies are currently under development, along with 800-plus non-genetically modified cell therapies, according to the American Society of Gene &#x26; Cell Therapy. And the development pipeline for monoclonal antibodies grew about 20% in 2022 to include 140 investigational drugs, estimates the Antibody Society.</p>
+      <div class="video-player">
+        <div>
+          <div>
+            <p>
+              <img src="https://vimeo.com/api/oembed.json?url=https%3A//vimeo.com/vimeo.com/video/842870177,842870177" alt="">
+            </p>
+            <p><a href="https://player.vimeo.com/video/842870177">https://player.vimeo.com/video/842870177</a></p>
+          </div>
+        </div>
+      </div>
+      <p>The demand for advanced therapeutics and new drug modalities is expected to explode in the coming decade. For example, more than 2,000 <a href="/us/en/library/gene-therapy.html">gene therapies</a> and modified <a href="/us/en/library/cell-therapy.html">cell therapies</a> are currently under development, along with 800-plus non-genetically modified cell therapies, according to the American Society of Gene &#x26; Cell Therapy. And the development pipeline for <a href="/us/en/library/monoclonal-antibodies-overview.html">monoclonal antibodies</a>grew about 20% in 2022 to include 140 investigational drugs, estimates the Antibody Society.</p>
       <p>While this is good news for patients awaiting treatments for complex diseases, it presents an immediate scalability challenge to biopharma leaders – one that University of Pennsylvania professor and CAR-T pioneer Dr. Carl June has referred to as a crisis waiting to happen. “My big worry is, what if we actually make … engineered cell therapies work for solid cancer?” June said during the Danaher Genomic Medicines Summit held in December 2022 in Boston. “We just couldn’t meet the demand at this point.”</p>
       <p>Indeed, biopharma leaders that are developing cell therapies and other potential cures for large patient populations will need to address bottlenecks in their research, development, and manufacturing processes to meet the expected demand.</p>
       <p>Several Life Sciences companies at Danaher Corporation, such as Molecular Devices, Leica Microsystems, SCIEX, IDBS, Beckman Coulter Life Sciences, Aldevron, and Cytiva, offer a wide array of products and services to support the biopharma industry at the point solution level, the automation level, and the data and digitization level. Together they help the industry to embrace an approach that combines scientific rigor with engineering know-how to create stronger innovation. This entails bolstering every stage of biopharma development with engineering principles and practices. Applying this approach will require biopharma developers to adopt automation at every stage, from early discovery through manufacturing, and to lean on artificial intelligence to improve their processes. And it will demand that best practices be industrialized to improve and accelerate the innovation of new cures.</p>
@@ -35,21 +43,27 @@ <h1>Enabling Science at Scale: How Danaher Life Sciences partners deep with Biop
       </div>
       <h2>About the Author</h2>
       <p>Vanessa Almendro, Ph.D, MBA, is Vice President of Science and Technology, Head of Innovation at Danaher Corporation, leading multiple initiatives to position Danaher at the forefront of innovation in science, technology, and medicine. Vanessa is also the Founder and Principal for the Brain Cancer Investment Fund, a philanthropic fund aiming at catalyzing the development of cures for brain cancer. Prior to Danaher, Vanessa was the Head of External Strategy and Innovation at the Eisai Center for Genetics Guided Dementia Discovery (G2D2). In this role, Vanessa led the creation of the Eisai Innovation Center Biolabs, the first incubator space specialized in neurology. She also led the development of academic affairs and external innovation strategies in concert with academic investigators, consortiums, biotech, and large pharmaceutical companies. Prior to this role, Vanessa worked as Head of Strategy and Operations for Cogen Immune Medicines, and she held multiple leadership roles at Vertex Pharmaceuticals both in the R&#x26;D and Commercial organizations. Prior to industry Vanessa was a Research fellow at the Dana-Farber Cancer Institute, Harvard Medical School and prior to that served as a Group Leader in the Department of Medical Oncology at IDIBAPS in Barcelona, Spain. Vanessa is a Ph.D. in Biochemistry and Molecular Biology from University of Barcelona, a Post-doc in Translational Medicine from the Dana Farber Cancer Institute, Harvard Medical School, and an Executive MBA from MIT-Sloan. She is a mentor for start-up companies at MassConnect, Nucleate Boston Activator, and a member of the Commercial Advisory Board for the School of Biomedical Engineering at UBC.</p>
-      <hr>
-      <div class="recent-articles">
-        <div>
-          <div></div>
-        </div>
-      </div>
       <div class="metadata">
         <div>
           <div>Title</div>
-          <div>Enabling Science at Scale: How Danaher Life Sciences partners deep with Biopharma | Danaher Life Sciences</div>
+          <div>Scaling Science: Danaher Life Sciences Solutions for Biopharma | Danaher Life Sciences</div>
         </div>
         <div>
           <div>canonical</div>
           <div><a href="https://lifesciences.danaher.com/us/en/blog/enabling-science-at-scale.html">https://lifesciences.danaher.com/us/en/blog/enabling-science-at-scale.html</a></div>
         </div>
+        <div>
+          <div>keywords</div>
+          <div>Next Gen Biomanufacturing</div>
+        </div>
+        <div>
+          <div>Tags</div>
+          <div>danaher:topics/next-gen-biomanufacturing</div>
+        </div>
+        <div>
+          <div>topics</div>
+          <div>Next Gen Biomanufacturing</div>
+        </div>
         <div>
           <div>Description</div>
           <div>The demand for advanced therapeutics and new drug modalities is expected to explode in the coming decade. For example, more than 2,000 gene therapies and modified cell therapies are currently under development, along with 800-plus non-genetically modified cell therapies, according to the American Society of Gene &#x26; Cell Therapy.</div>
@@ -60,7 +74,7 @@ <h2>About the Author</h2>
         </div>
         <div>
           <div>authorTitle</div>
-          <div>Vice President of Science and Technology, Head of Innovation, Danaher Corporation</div>
+          <div>Vice President of Science and Technology, Head of Innovation</div>
         </div>
         <div>
           <div>publishDate</div>
@@ -72,17 +86,21 @@ <h2>About the Author</h2>
             <img src="https://author-dummy.adobeaemcloud.com/content/dam/danaher/blogs/external-blogs/enabling-science-at-scale/vanessa-almendro.jpeg" alt="">
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+        <div>
+          <div>brand</div>
+          <div>Danaher</div>
+        </div>
         <div>
           <div>readingTime</div>
           <div>8</div>
         </div>
         <div>
           <div>creationDate</div>
-          <div>Thu, 31 Aug 2023 13:25:52 GMT</div>
+          <div>Thu, 01 Feb 2024 15:32:54 GMT</div>
         </div>
         <div>
           <div>updateDate</div>
-          <div>Wed, 18 Oct 2023 10:40:03 GMT</div>
+          <div>Mon, 27 May 2024 07:02:32 GMT</div>
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@@ -444,7 +526,8 @@
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+</div>
 </div>
 
 
@@ -452,7 +535,7 @@
     
     <div class="articleinfo">
 
-	<articleinfo articleimage="/content/dam/danaher/blogs/external-blogs/enabling-science-at-scale/vanessa-almendro.jpeg" alttext="vanessa-almendro" articlename="Vanessa Almendro" title="Vice President of Science and Technology, Head of Innovation, Danaher Corporation" postdate="22 June, 2023" time="8 Mins">
+	<articleinfo articleimage="/content/dam/danaher/blogs/external-blogs/enabling-science-at-scale/vanessa-almendro.jpeg" alttext="vanessa-almendro" articlename="Vanessa Almendro" title="Vice President of Science and Technology, Head of Innovation" opco=" Danaher" postdate="22 June, 2023" time="8 Mins">
 	</articleinfo>
 
 </div>
@@ -462,7 +545,7 @@
     
     <div class="featureimage">
 
-    <feature-image textwidth="_self" titlesize="xl" description="&lt;p>The demand for advanced therapeutics and new drug modalities is expected to explode in the coming decade. For example, more than 2,000 gene therapies and modified cell therapies are currently under development, along with 800-plus non-genetically modified cell therapies, according to the American Society of Gene &amp;amp; Cell Therapy. And the development pipeline for monoclonal antibodies grew about 20% in 2022 to include 140 investigational drugs, estimates the Antibody Society.&lt;/p>
+    <feature-image textwidth="_self" titlesize="xl" titleheading="h1" description="&lt;p>The demand for advanced therapeutics and new drug modalities is expected to explode in the coming decade. For example, more than 2,000 &lt;a href=&#34;/content/danaher/ls/us/en/library/gene-therapy.html&#34;>&lt;b>gene therapies&lt;/b>&lt;/a> and modified &lt;a href=&#34;/content/danaher/ls/us/en/library/cell-therapy.html&#34;>&lt;b>cell therapies&lt;/b>&lt;/a> are currently under development, along with 800-plus non-genetically modified cell therapies, according to the American Society of Gene &amp;amp; Cell Therapy. And the development pipeline for &lt;b>&lt;a href=&#34;/content/danaher/ls/us/en/library/monoclonal-antibodies-overview.html&#34;>monoclonal antibodies&lt;/a> &lt;/b>grew about 20% in 2022 to include 140 investigational drugs, estimates the Antibody Society.&lt;/p>
 &lt;p>While this is good news for patients awaiting treatments for complex diseases, it presents an immediate scalability challenge to biopharma leaders – one that University of Pennsylvania professor and CAR-T pioneer Dr. Carl June has referred to as a crisis waiting to happen. “My big worry is, what if we actually make … engineered cell therapies work for solid cancer?” June said during the Danaher Genomic Medicines Summit held in December 2022 in Boston. “We just couldn’t meet the demand at this point.”&lt;/p>
 &lt;p>&amp;nbsp;&lt;/p>
 &lt;p>Indeed, biopharma leaders that are developing cell therapies and other potential cures for large patient populations will need to address bottlenecks in their research, development, and manufacturing processes to meet the expected demand.&lt;/p>
@@ -472,6 +555,7 @@
 &lt;p>Danaher Life Sciences partners deep with biopharma companies like Sanofi to help solve the oldest and most vexing challenges in biopharma: the high rate of failure of drugs that look promising in phase 1 trials but never make it to market, and the excessive time it takes to discover new medicines and deliver them to patients.&lt;/p>
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+
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@@ -520,6 +604,7 @@
     <feature-image textwidth="_self" title="About the Author" titlesize="xl" description="&lt;p>Vanessa Almendro, Ph.D, MBA, is Vice President of Science and Technology, Head of Innovation at Danaher Corporation, leading multiple initiatives to position Danaher at the forefront of innovation in science, technology, and medicine. Vanessa is also the Founder and Principal for the Brain Cancer Investment Fund, a philanthropic fund aiming at catalyzing the development of cures for brain cancer. Prior to Danaher, Vanessa was the Head of External Strategy and Innovation at the Eisai Center for Genetics Guided Dementia Discovery (G2D2). In this role, Vanessa led the creation of the Eisai Innovation Center Biolabs, the first incubator space specialized in neurology. She also led the development of academic affairs and external innovation strategies in concert with academic investigators, consortiums, biotech, and large pharmaceutical companies. Prior to this role, Vanessa worked as Head of Strategy and Operations for Cogen Immune Medicines, and she held multiple leadership roles at Vertex Pharmaceuticals both in the R&amp;amp;D and Commercial organizations. Prior to industry Vanessa was a Research fellow at the Dana-Farber Cancer Institute, Harvard Medical School and prior to that served as a Group Leader in the Department of Medical Oncology at IDIBAPS in Barcelona, Spain. Vanessa is a Ph.D. in Biochemistry and Molecular Biology from University of Barcelona, a Post-doc in Translational Medicine from the Dana Farber Cancer Institute, Harvard Medical School, and an Executive MBA from MIT-Sloan. She is a mentor for start-up companies at MassConnect, Nucleate Boston Activator, and a member of the Commercial Advisory Board for the School of Biomedical Engineering at UBC.&lt;/p>
 " descsize="tbase" btnnewtab="_self">
     </feature-image>
+
 </div>
 
 
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 <div class="aem-Grid aem-Grid--12 aem-Grid--default--12 ">
     
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-
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-
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-
     
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 <div class="script">
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-  <footer class="bg-danaherpurple-800" aria-labelledby="footer-heading">
+  <footer class="bg-danaherpurple-50" aria-labelledby="footer-heading">
     <p id="footer-heading" class="sr-only">Footer</p>
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         <div class="mt-12 md:mt-0">
-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Solutions</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Solutions</p>
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+              <a href="/us/en/solutions/mabs/cell-line-development.html" class="text-base hover:text-danaherpurple-800 hover:underline">Cell Line Development</a>
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-              <a href="/us/en/solutions/mrna-therapy.html" class="text-base text-white hover:text-danaherpurple-50 ">mRNA Development</a>
+              <a href="/us/en/solutions/mrna-therapy.html" class="text-base hover:text-danaherpurple-800 hover:underline">mRNA Development</a>
             </li>
             <li>
-              <a href="/us/en/solutions/oligonucleotide-therapy/antisense-oligonucleotide-development-manufacturing.html" class="text-base text-white hover:text-danaherpurple-50 ">Antisense Oligonucleotide</a>
+              <a href="/us/en/solutions/oligonucleotide-therapy/antisense-oligonucleotide-development-manufacturing.html" class="text-base hover:text-danaherpurple-800 hover:underline">Antisense Oligonucleotide</a>
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-              <a href="/us/en/solutions/pdna-synthesis.html" class="text-base text-white hover:text-danaherpurple-50 ">pDNA Synthesis</a>
+              <a href="/us/en/solutions/pdna-synthesis.html" class="text-base hover:text-danaherpurple-800 hover:underline">pDNA Synthesis</a>
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-              <a href="/us/en/solutions/cell-therapy.html" class="text-base text-white hover:text-danaherpurple-50 ">Cell Therapy</a>
+              <a href="/us/en/solutions/small-molecule-drug-discovery.html" class="text-base hover:text-danaherpurple-800 hover:underline">Small Molecules</a>
+            </li>            
+            <li>
+              <a href="/us/en/solutions/cell-therapy.html" class="text-base hover:text-danaherpurple-800 hover:underline">Cell Therapy</a>
             </li>
             <li>
-              <a href="/us/en/solutions/gene-therapy.html" class="text-base text-white hover:text-danaherpurple-50 ">Gene Therapy</a>
+              <a href="/us/en/solutions/gene-therapy.html" class="text-base hover:text-danaherpurple-800 hover:underline">Gene Therapy</a>
             </li>
           </ul>
         </div>
         <div class="mt-12 md:mt-0">
-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Explore</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Explore</p>
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-              <a href="/us/en/products.html" class="text-base text-white hover:text-danaherpurple-50">Products</a>
+              <a href="/us/en/products.html" class="text-base hover:text-danaherpurple-800 hover:underline">Products</a>
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             <li>
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+              <a href="/us/en/solutions.html" class="text-base hover:text-danaherpurple-800 hover:underline">Solutions</a>
             </li>
             <li>
-              <a href="/us/en/application.html" class="text-base text-white hover:text-danaherpurple-50">Applications</a>
+              <a href="/us/en/application.html" class="text-base hover:text-danaherpurple-800 hover:underline">Applications</a>
             </li>
             <li>
-              <a href="/us/en/library.html" class="text-base text-white hover:text-danaherpurple-50">Technical Library</a>
+              <a href="/us/en/library.html" class="text-base hover:text-danaherpurple-800 hover:underline">Technical Library</a>
             </li>
             <li>
-              <a href="/us/en/expert.html" class="text-base text-white hover:text-danaherpurple-50">Talk
+              <a href="/us/en/expert.html" class="text-base hover:text-danaherpurple-800 hover:underline">Talk
                 to an Expert</a>
             </li>
             <li>
-              <a href="/us/en/quote-cart.html" class="text-base text-white hover:text-danaherpurple-50">Request a Quote</a>
+              <a href="/us/en/quote-cart.html" class="text-base hover:text-danaherpurple-800 hover:underline">Request a Quote</a>
             </li>
           </ul>
         </div>
         <div class="mt-12 md:mt-0">
-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Company</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Company</p>
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             <li>
-              <a href="/us/en/about-us.html" class="text-base text-white hover:text-danaherpurple-50">About</a>
+              <a href="/us/en/about-us.html" class="text-base hover:text-danaherpurple-800 hover:underline">About</a>
             </li>
             <li>
-              <a href="/us/en/news.html" class="text-base text-white hover:text-danaherpurple-50">News</a>
+              <a href="/us/en/news.html" class="text-base hover:text-danaherpurple-800 hover:underline">News</a>
             </li>
             <li>
-              <a href="/us/en/blog.html" class="text-base text-white hover:text-danaherpurple-50">Blog</a>
+              <a href="/us/en/blog.html" class="text-base hover:text-danaherpurple-800 hover:underline">Blog</a>
             </li>
             <li>
-              <a href="https://jobs.danaher.com/global/en?utm_source=dhls_website&utm_medium=referral&utm_content=footer" class="text-base text-white hover:text-danaherpurple-50">Careers</a>
+              <a href="https://jobs.danaher.com/global/en?utm_source=dhls_website&utm_medium=referral&utm_content=footer" class="text-base hover:text-danaherpurple-800 hover:underline">Careers</a>
             </li>
           </ul>
         </div>
         <div class="mt-12 md:mt-0">
-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Legal</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Legal</p>
           <ul role="list" class="mt-4 space-y-4">
             <li>
-              <a href="/us/en/legal/cookies.html" class="text-base text-white hover:text-danaherpurple-50 ">Cookie Policy</a>
+              <a href="/us/en/legal/cookies.html" class="text-base hover:text-danaherpurple-800 hover:underline">Cookie Policy</a>
             </li>
             <li>
-              <a href="/us/en/legal/ccpa.html" class="text-base text-white hover:text-danaherpurple-50">Do Not Sell or Share My Data</a>
+              <a href="/us/en/legal/ccpa.html" class="text-base hover:text-danaherpurple-800 hover:underline">Do Not Sell or Share My Data</a>
             </li>
             <li>
-              <a href="#" class="text-base text-white hover:text-danaherpurple-50 ot-sdk-show-settings">Manage Cookies</a>
+              <a href="#" class="text-base hover:text-danaherpurple-800 hover:underlineot-sdk-show-settings">Manage Cookies</a>
             </li>
             <li>
-              <a href="/us/en/legal/privacy-policy.html" class="text-base text-white hover:text-danaherpurple-50">Privacy Policy</a>
+              <a href="/us/en/legal/privacy-policy.html" class="text-base hover:text-danaherpurple-800 hover:underline">Privacy Policy</a>
             </li>
             <li>
-              <a href="/us/en/legal/terms-of-use.html" class="text-base text-white hover:text-danaherpurple-50">Terms of Use</a>
+              <a href="/us/en/legal/terms-of-use.html" class="text-base hover:text-danaherpurple-800 hover:underline">Terms of Use</a>
             </li>
           </ul>
         </div>
@@ -795,13 +874,13 @@
 
       <div class="mt-8 border-t border-danaherpurple-500 pt-8 sm:mt-8 lg:mt-8 lg:flex lg:items-center lg:justify-between">
         <div>
-          <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe to our newsletter</h3>
-          <p class="mt-2 leading-6 text-base text-white">The latest news, articles, and resources, sent to your inbox
+          <h3 class="text-sm font-semibold tracking-wider uppercase">Subscribe to our newsletter</h3>
+          <p class="mt-2 leading-6 text-base">The latest news, articles, and resources, sent to your inbox
             weekly.</p>
         </div>
         <div class="mt-6 sm:flex sm:max-w-md lg:mt-0">
           <div class="mt-4 sm:ml-4 sm:mt-0 sm:flex-shrink-0">
-            <a href="/us/en/connect/newsletter.html" class="btn border-2 px-8 my-auto ml-auto btn-primary">Subscribe</a>
+            <a href="/us/en/connect/newsletter.html" class="btn border-2 px-8 my-auto ml-auto btn-outline-trending-brand">Subscribe</a>
           </div>
         </div>
       </div>
@@ -810,41 +889,15 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
         <div class="flex space-x-6 md:order-2">
           <a href="https://www.linkedin.com/company/danaher-life-sciences/" class="text-gray-500 hover:text-danaherpurple-50">
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+            <svg xmlns="http://www.w3.org/2000/svg" width="24" height="24" viewBox="0 0 24 24"><path d="M4.98 3.5c0 1.381-1.11 2.5-2.48 2.5s-2.48-1.119-2.48-2.5c0-1.38 1.11-2.5 2.48-2.5s2.48 1.12 2.48 2.5zm.02 4.5h-5v16h5v-16zm7.982 0h-4.968v16h4.969v-8.399c0-4.67 6.029-5.052 6.029 0v8.399h4.988v-10.131c0-7.88-8.922-7.593-11.018-3.714v-2.155z"/></svg>
           </a>
         </div>
-        <p class="mt-8 text-base text-white md:mt-0 md:order-1"> © 2023 DH Life Sciences, LLC. All Rights Reserved.
+        <p class="mt-8 text-base md:mt-0 md:order-1"> © 2024 DH Life Sciences, LLC. All Rights Reserved.
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     </div>
   </footer>
 </div></div>
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-
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-
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@@ -888,7 +941,7 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
 
     
     
-<script src="/etc.clientlibs/core/wcm/components/commons/datalayer/v1/clientlibs/core.wcm.components.commons.datalayer.v1.lc-904d3c2f1e821ab45124d66de422b409-lc.min.js"></script>
+<script src="/etc.clientlibs/core/wcm/components/commons/datalayer/v1/clientlibs/core.wcm.components.commons.datalayer.v1.lc-70264651675213ed7f7cc5a02a00f621-lc.min.js"></script>
 
 
 
@@ -898,14 +951,14 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
         
     
 <script src="/etc.clientlibs/core/wcm/components/commons/site/clientlibs/container.lc-0a6aff292f5cc42142779cde92054524-lc.min.js"></script>
-<script src="/etc.clientlibs/danaher/clientlibs/clientlib-base.lc-214c895a1b8622f2c43e2f18809e051a-lc.min.js"></script>
+<script src="/etc.clientlibs/danaher/clientlibs/clientlib-base.lc-2a85512656f79a4d72626fea0d606318-lc.min.js"></script>
 
 
 
 
     
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+<script src="/etc.clientlibs/danaher/clientlibs/clientlib-site.lc-26d30872729a07b9af9948e2214046af-lc.min.js"></script>
 
 
 
@@ -976,6 +1029,8 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
 
 </script>
 
+<script src="https://cdn.usefathom.com/script.js" data-site="KGTBOGMR" defer></script>
+
 
     
 </body>
diff --git a/tools/actions/convert/test/fixtures/product1-converted.html b/tools/actions/convert/test/fixtures/product1-converted.html
index 9fb79e1c4..b58729cae 100644
--- a/tools/actions/convert/test/fixtures/product1-converted.html
+++ b/tools/actions/convert/test/fixtures/product1-converted.html
@@ -24,7 +24,7 @@ <h2>Next-generation fluorescent imaging solution for the assurance of monoclonal
       <p>Demonstrating that cell lines are monoclonal – or that a gene was edited as expected – can be a time-consuming and highly-subjective process when relying on conventional technologies. The CloneSelect® Imager and CloneSelect® Imager FL are high-throughput automated solutions for imaging and analyzing mammalian cells. Tracking the formation of a colony from a single cell is effortless as barcoded plates are tracked over time. Automated acquisition and analysis provides accurate, objective, and consistent results.</p>
       <p>With high-resolution white light imaging, the CloneSelect Imager provides automated confluence, monoclonality assurance and industry-leading acquisition times with the ability to image a 96-well plate in under two minutes.</p>
       <p>The all-new CloneSelect Imager FL features high-contrast multichannel fluorescent and white light imaging that allows for accurate single-cell detection and proof of monoclonality at day 0. Streamline your workflow with comparative confluence assays to identify and verify gene edits.</p>
-      <div class="columns">
+      <div class="columns features-card-left">
         <div>
           <div>
             <p>:dam-check-box:</p>
@@ -37,10 +37,27 @@ <h2>Next-generation fluorescent imaging solution for the assurance of monoclonal
             <p><strong>Rapid single-cell confirmation</strong></p>
             <p>The imager delivers industry-leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence.</p>
           </div>
-          <div><a href="https://play.vidyard.com/WwWUddqbVhBk8jtmGQ6dHF.html">Video Player</a></div>
+          <div>
+            <table>
+              <thead>
+                <tr>
+                  <th>Video Player</th>
+                </tr>
+              </thead>
+              <tbody>
+                <tr>
+                  <td>
+                    <p>
+                      <img src="http://share.vidyard.com/watch/WwWUddqbVhBk8jtmGQ6dHF.html" alt="">
+                    </p>
+                    <p><a href="https://play.vidyard.com/WwWUddqbVhBk8jtmGQ6dHF.html">https://play.vidyard.com/WwWUddqbVhBk8jtmGQ6dHF.html</a></p>
+                  </td>
+                </tr>
+              </tbody>
+            </table>
+          </div>
         </div>
       </div>
-      <h2>Highlights</h2>
       <div class="columns cols-3">
         <div>
           <div>
@@ -91,7 +108,6 @@ <h2>CloneSelect Imager FL</h2>
           </div>
         </div>
       </div>
-      <h2>Streamlined Workflow</h2>
       <div class="product-menu">
         <div>
           <div>
@@ -143,7 +159,7 @@ <h2>Streamlined Workflow</h2>
       <div class="section-metadata">
         <div>
           <div>tabIcon</div>
-          <div>/content/dam/danaher/system/icons/Chart bar.svg</div>
+          <div>/content/dam/danaher/system/icons/Chart-bar.svg</div>
         </div>
         <div>
           <div>tabName</div>
@@ -191,7 +207,7 @@ <h2>Streamlined Workflow</h2>
       <div class="section-metadata">
         <div>
           <div>tabIcon</div>
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The CloneSelect\\u00ae Imager and CloneSelect\\u00ae Imager FL are a high-throughput automated solutions for imaging and analyzing mammalian cells. Tracking the formation of a colony from a single cell is effortless as barcoded plates are tracked over time. Automated acquisition and analysis provides accurate, objective, and consistent results.\\n\\nWith high-resolution white light imaging, the CloneSelect Imager provides automated confluence, monoclonality assurance and industry leading acquisition times with the ability to image a 96-well plate in under two minutes.\\n\\nThe all new CloneSelect Imager FL features high contrast multichannel fluorescent and white light imaging that allows for accurate single cell detection and proof of monoclonality at day 0. Streamline your workflow with comparative confluence assays to identify and verify gene edits.\\n\\nDemonstrated IND success\\nThe Monoclonality Report feature streamlines the creation of supporting documentation for regulatory agencies. Reports are automatically generated based on parameters you select. The Monoclonality Report is an audit-ready document that supports filing for an Investigational New Drug (IND) Application with the FDA. (21 CFR Part 312)\\n\\nMultichannel imaging and automated confluence\\nAlgorithms are optimized for accurate cell detection and address varying cell types and conditions. Publication-ready high-resolution imaging provides automatic confluence analysis and monoclonality assurance.\\n\\nRapid single cell confirmation\\nThe imager delivers industry leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence.\\n\\n\\n\\nFeatures\\nWhite light and fluorescent imaging\\nImage every well in every plate with rapid acquisition times with label-free white light. Multichannel fluorescence imaging provides additional confidence of monoclonality and comparative confluence assays (red vs green).\\n\\nData tools to accelerate research timelines\\nThe software automatically calculates confluence measurements and generates growth curves, heatmaps, and image montages. Measurements for every well are automatically tracked over time. Streamline multiple steps (imaging, sample tracking, data analysis and report generation) in the cell line development workflow for IND filing.\\n\\nQuickly image a variety of plate formats and cell types\\nImage a 96-well plate in under two minutes. Compatible with adherent or settled suspension cell types such as CHO, HEK, hybridomas, iPSCs, and many other cell types.\\n\\nIntelligent analysis with easy-to-use software\\nThe software automatically calculates confluence for each imaging time point. Growth curve, image montage, total growth, and mean rate are generated automatically and are exportable. Guided software user interface allows for simple 1-hour training.\\n\\nHigh-resolution images\\nHigh-speed fluorescence and high-resolution white light imaging with accurate detection of single cells including debris. Image visualization and data tracking over multiple days.\\n\\nCustom automation options*\\nThe Automation and Customization Team offers a variety of custom services from robotic plate loading to fully automated workstations with liquid handling and incubation. We have built out custom automated work cells with the CloneSelect Imager for iPSC workflows, full assay systems and drug toxicity and characterization research.\\n\\n*Price, time to deliver and specifications will vary based on mutually agreed technical requirements. Solution requirements may cause adjustment to standard performance.\&#34;], \&#34;metadescription\&#34;: [\&#34;\&#34;], \&#34;richdescription\&#34;: [\&#34;&lt;h4>High-speed fluorescence and white light imaging, intelligent data analysis, and monoclonality report generation&lt;/h4>\&#34;], \&#34;lastenrichmentdate\&#34;: [\&#34;2023-12-14 16:08:04.4684827\&#34;], \&#34;defaultcategoryname\&#34;: [\&#34;Single-Cell Imaging Systems\&#34;], \&#34;richlongdescription\&#34;: [\&#34;&lt;h3>Next-generation fluorescent imaging solution for the assurance of monoclonality and automated confluence across diverse cell types&lt;/h3>\\n&lt;p>Demonstrating that cell lines are monoclonal &amp;ndash; or that a gene was edited as expected &amp;ndash; can be a time-consuming and highly-subjective process when relying on conventional technologies. The CloneSelect&amp;reg; Imager and CloneSelect&amp;reg; Imager FL are a high-throughput automated solutions for imaging and analyzing mammalian cells. Tracking the formation of a colony from a single cell is effortless as barcoded plates are tracked over time. Automated acquisition and analysis provides accurate, objective, and consistent results.&lt;/p>\\n&lt;p>With high-resolution white light imaging, the CloneSelect Imager provides automated confluence, monoclonality assurance and industry leading acquisition times with the ability to image a 96-well plate in under two minutes.&lt;/p>\\n&lt;p>The all new CloneSelect Imager FL features high contrast multichannel fluorescent and white light imaging that allows for accurate single cell detection and proof of monoclonality at day 0. Streamline your workflow with comparative confluence assays to identify and verify gene edits.&lt;/p>\\n&lt;ul>\\n&lt;li>\\n&lt;h4>Demonstrated IND success&lt;/h4>\\n&lt;p>The Monoclonality Report feature streamlines the creation of supporting documentation for regulatory agencies. Reports are automatically generated based on parameters you select. The Monoclonality Report is an audit-ready document that supports filing for an Investigational New Drug (IND) Application with the FDA. (21 CFR Part 312)&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Multichannel imaging and automated confluence&lt;/h4>\\n&lt;p>Algorithms are optimized for accurate cell detection and address varying cell types and conditions. Publication-ready high-resolution imaging provides automatic confluence analysis and monoclonality assurance.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Rapid single cell confirmation&lt;/h4>\\n&lt;p>The imager delivers industry leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence.&lt;/p>\\n&lt;/li>\\n&lt;/ul>\\n&lt;p>&amp;nbsp;&lt;/p>\\n&lt;h3>Features&lt;/h3>\\n&lt;ul>\\n&lt;li>\\n&lt;h4>White light and fluorescent imaging&lt;/h4>\\n&lt;p>Image every well in every plate with rapid acquisition times with label-free white light. Multichannel fluorescence imaging provides additional confidence of monoclonality and comparative confluence assays (red vs green).&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Data tools to accelerate research timelines&lt;/h4>\\n&lt;p>The software automatically calculates confluence measurements and generates growth curves, heatmaps, and image montages. Measurements for every well are automatically tracked over time. Streamline multiple steps (imaging, sample tracking, data analysis and report generation) in the cell line development workflow for IND filing.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Quickly image a variety of plate formats and cell types&lt;/h4>\\n&lt;p>Image a 96-well plate in under two minutes. Compatible with adherent or settled suspension cell types such as CHO, HEK, hybridomas, iPSCs, and many other cell types.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Intelligent analysis with easy-to-use software&lt;/h4>\\n&lt;p>The software automatically calculates confluence for each imaging time point. Growth curve, image montage, total growth, and mean rate are generated automatically and are exportable. Guided software user interface allows for simple 1-hour training.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>High-resolution images&lt;/h4>\\n&lt;p>High-speed fluorescence and high-resolution white light imaging with accurate detection of single cells including debris. Image visualization and data tracking over multiple days.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Custom automation options*&lt;/h4>\\n&lt;p>The Automation and Customization Team offers a variety of custom services from robotic plate loading to fully automated workstations with liquid handling and incubation. 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Streamline multiple steps (imaging, sample tracking, data analysis and report generation) in the cell line development workflow for IND filing.\\n\\nQuickly image a variety of plate formats and cell types\\nImage a 96-well plate in under two minutes. Compatible with adherent or settled suspension cell types such as CHO, HEK, hybridomas, iPSCs, and many other cell types.\\n\\nIntelligent analysis with easy-to-use software\\nThe software automatically calculates confluence for each imaging time point. Growth curve, image montage, total growth, and mean rate are generated automatically and are exportable. Guided software user interface allows for simple 1-hour training.\\n\\nHigh-resolution images\\nHigh-speed fluorescence and high-resolution white light imaging with accurate detection of single cells including debris. Image visualization and data tracking over multiple days.\\n\\nCustom automation options*\\nThe Automation and Customization Team offers a variety of custom services from robotic plate loading to fully automated workstations with liquid handling and incubation. We have built out custom automated work cells with the CloneSelect Imager for iPSC workflows, full assay systems and drug toxicity and characterization research.\\n\\n*Price, time to deliver and specifications will vary based on mutually agreed technical requirements. Solution requirements may cause adjustment to standard performance.\&#34;], \&#34;defaultcategory\&#34;: [\&#34;clone-screening-systems/single-cell-imaging-systems\&#34;], \&#34;longdescription\&#34;: [\&#34;Next-generation fluorescent imaging solution for the assurance of monoclonality and automated confluence across diverse cell types\\nDemonstrating that cell lines are monoclonal \\u2013 or that a gene was edited as expected \\u2013 can be a time-consuming and highly-subjective process when relying on conventional technologies. The CloneSelect\\u00ae Imager and CloneSelect\\u00ae Imager FL are a high-throughput automated solutions for imaging and analyzing mammalian cells. Tracking the formation of a colony from a single cell is effortless as barcoded plates are tracked over time. Automated acquisition and analysis provides accurate, objective, and consistent results.\\n\\nWith high-resolution white light imaging, the CloneSelect Imager provides automated confluence, monoclonality assurance and industry leading acquisition times with the ability to image a 96-well plate in under two minutes.\\n\\nThe all new CloneSelect Imager FL features high contrast multichannel fluorescent and white light imaging that allows for accurate single cell detection and proof of monoclonality at day 0. Streamline your workflow with comparative confluence assays to identify and verify gene edits.\\n\\nDemonstrated IND success\\nThe Monoclonality Report feature streamlines the creation of supporting documentation for regulatory agencies. Reports are automatically generated based on parameters you select. The Monoclonality Report is an audit-ready document that supports filing for an Investigational New Drug (IND) Application with the FDA. (21 CFR Part 312)\\n\\nMultichannel imaging and automated confluence\\nAlgorithms are optimized for accurate cell detection and address varying cell types and conditions. Publication-ready high-resolution imaging provides automatic confluence analysis and monoclonality assurance.\\n\\nRapid single cell confirmation\\nThe imager delivers industry leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence.\\n\\n\\n\\nFeatures\\nWhite light and fluorescent imaging\\nImage every well in every plate with rapid acquisition times with label-free white light. Multichannel fluorescence imaging provides additional confidence of monoclonality and comparative confluence assays (red vs green).\\n\\nData tools to accelerate research timelines\\nThe software automatically calculates confluence measurements and generates growth curves, heatmaps, and image montages. Measurements for every well are automatically tracked over time. Streamline multiple steps (imaging, sample tracking, data analysis and report generation) in the cell line development workflow for IND filing.\\n\\nQuickly image a variety of plate formats and cell types\\nImage a 96-well plate in under two minutes. Compatible with adherent or settled suspension cell types such as CHO, HEK, hybridomas, iPSCs, and many other cell types.\\n\\nIntelligent analysis with easy-to-use software\\nThe software automatically calculates confluence for each imaging time point. Growth curve, image montage, total growth, and mean rate are generated automatically and are exportable. Guided software user interface allows for simple 1-hour training.\\n\\nHigh-resolution images\\nHigh-speed fluorescence and high-resolution white light imaging with accurate detection of single cells including debris. Image visualization and data tracking over multiple days.\\n\\nCustom automation options*\\nThe Automation and Customization Team offers a variety of custom services from robotic plate loading to fully automated workstations with liquid handling and incubation. We have built out custom automated work cells with the CloneSelect Imager for iPSC workflows, full assay systems and drug toxicity and characterization research.\\n\\n*Price, time to deliver and specifications will vary based on mutually agreed technical requirements. Solution requirements may cause adjustment to standard performance.\&#34;], \&#34;richdescription\&#34;: [\&#34;&lt;h4>High-speed fluorescence and white light imaging, intelligent data analysis, and monoclonality report generation&lt;/h4>\&#34;], \&#34;numspecifications\&#34;: [0], \&#34;specificationsjson\&#34;: [\&#34;{}\&#34;], \&#34;defaultcategoryname\&#34;: [\&#34;Single-Cell Imaging Systems\&#34;], \&#34;richlongdescription\&#34;: [\&#34;&lt;h3>Next-generation fluorescent imaging solution for the assurance of monoclonality and automated confluence across diverse cell types&lt;/h3>\\n&lt;p>Demonstrating that cell lines are monoclonal &amp;ndash; or that a gene was edited as expected &amp;ndash; can be a time-consuming and highly-subjective process when relying on conventional technologies. The CloneSelect&amp;reg; Imager and CloneSelect&amp;reg; Imager FL are a high-throughput automated solutions for imaging and analyzing mammalian cells. Tracking the formation of a colony from a single cell is effortless as barcoded plates are tracked over time. Automated acquisition and analysis provides accurate, objective, and consistent results.&lt;/p>\\n&lt;p>With high-resolution white light imaging, the CloneSelect Imager provides automated confluence, monoclonality assurance and industry leading acquisition times with the ability to image a 96-well plate in under two minutes.&lt;/p>\\n&lt;p>The all new CloneSelect Imager FL features high contrast multichannel fluorescent and white light imaging that allows for accurate single cell detection and proof of monoclonality at day 0. Streamline your workflow with comparative confluence assays to identify and verify gene edits.&lt;/p>\\n&lt;ul>\\n&lt;li>\\n&lt;h4>Demonstrated IND success&lt;/h4>\\n&lt;p>The Monoclonality Report feature streamlines the creation of supporting documentation for regulatory agencies. Reports are automatically generated based on parameters you select. The Monoclonality Report is an audit-ready document that supports filing for an Investigational New Drug (IND) Application with the FDA. (21 CFR Part 312)&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Multichannel imaging and automated confluence&lt;/h4>\\n&lt;p>Algorithms are optimized for accurate cell detection and address varying cell types and conditions. Publication-ready high-resolution imaging provides automatic confluence analysis and monoclonality assurance.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Rapid single cell confirmation&lt;/h4>\\n&lt;p>The imager delivers industry leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence.&lt;/p>\\n&lt;/li>\\n&lt;/ul>\\n&lt;p>&amp;nbsp;&lt;/p>\\n&lt;h3>Features&lt;/h3>\\n&lt;ul>\\n&lt;li>\\n&lt;h4>White light and fluorescent imaging&lt;/h4>\\n&lt;p>Image every well in every plate with rapid acquisition times with label-free white light. Multichannel fluorescence imaging provides additional confidence of monoclonality and comparative confluence assays (red vs green).&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Data tools to accelerate research timelines&lt;/h4>\\n&lt;p>The software automatically calculates confluence measurements and generates growth curves, heatmaps, and image montages. Measurements for every well are automatically tracked over time. Streamline multiple steps (imaging, sample tracking, data analysis and report generation) in the cell line development workflow for IND filing.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Quickly image a variety of plate formats and cell types&lt;/h4>\\n&lt;p>Image a 96-well plate in under two minutes. Compatible with adherent or settled suspension cell types such as CHO, HEK, hybridomas, iPSCs, and many other cell types.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Intelligent analysis with easy-to-use software&lt;/h4>\\n&lt;p>The software automatically calculates confluence for each imaging time point. Growth curve, image montage, total growth, and mean rate are generated automatically and are exportable. Guided software user interface allows for simple 1-hour training.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>High-resolution images&lt;/h4>\\n&lt;p>High-speed fluorescence and high-resolution white light imaging with accurate detection of single cells including debris. Image visualization and data tracking over multiple days.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Custom automation options*&lt;/h4>\\n&lt;p>The Automation and Customization Team offers a variety of custom services from robotic plate loading to fully automated workstations with liquid handling and incubation. We have built out custom automated work cells with the CloneSelect Imager for iPSC workflows, full assay systems and drug toxicity and characterization research.&lt;/p>\\n&lt;p>&lt;em>*Price, time to deliver and specifications will vary based on mutually agreed technical requirements. Solution requirements may cause adjustment to standard performance.&lt;/em>&lt;/p>\\n&lt;/li>\\n&lt;/ul>\&#34;]}}, {\&#34;Origin\&#34;: \&#34;field decomposition\&#34;, \&#34;Values\&#34;: {\&#34;decomposed_sku\&#34;: [\&#34;clonese\&#34;, \&#34;cloneselectimagers\&#34;, \&#34;cloneselectimag\&#34;, \&#34;cloneselectimager\&#34;, \&#34;clonesele\&#34;, \&#34;clon\&#34;, \&#34;clo\&#34;, \&#34;clones\&#34;, \&#34;cloneselec\&#34;, \&#34;cloneselect\&#34;, \&#34;clonesel\&#34;, \&#34;cloneselectimage\&#34;, \&#34;cloneselectim\&#34;, \&#34;cloneselectima\&#34;, \&#34;clone\&#34;, \&#34;cloneselecti\&#34;], \&#34;decomposed_productid\&#34;: [\&#34;clonese\&#34;, \&#34;cloneselectimagers\&#34;, \&#34;cloneselectimag\&#34;, \&#34;cloneselectimager\&#34;, \&#34;clonesele\&#34;, \&#34;clon\&#34;, \&#34;clo\&#34;, \&#34;clones\&#34;, \&#34;cloneselec\&#34;, \&#34;cloneselect\&#34;, \&#34;clonesel\&#34;, \&#34;cloneselectimage\&#34;, \&#34;cloneselectim\&#34;, \&#34;cloneselectima\&#34;, \&#34;clone\&#34;, \&#34;cloneselecti\&#34;]}}, {\&#34;Origin\&#34;: \&#34;view all metadata\&#34;, \&#34;Values\&#34;: {}}]&#34;,&#34;richlongdescription&#34;:&#34;&lt;h3>Next-generation fluorescent imaging solution for the assurance of monoclonality and automated confluence across diverse cell types&lt;/h3>\n&lt;p>Demonstrating that cell lines are monoclonal &amp;ndash; or that a gene was edited as expected &amp;ndash; can be a time-consuming and highly-subjective process when relying on conventional technologies. The CloneSelect&amp;reg; Imager and CloneSelect&amp;reg; Imager FL are a high-throughput automated solutions for imaging and analyzing mammalian cells. Tracking the formation of a colony from a single cell is effortless as barcoded plates are tracked over time. Automated acquisition and analysis provides accurate, objective, and consistent results.&lt;/p>\n&lt;p>With high-resolution white light imaging, the CloneSelect Imager provides automated confluence, monoclonality assurance and industry leading acquisition times with the ability to image a 96-well plate in under two minutes.&lt;/p>\n&lt;p>The all new CloneSelect Imager FL features high contrast multichannel fluorescent and white light imaging that allows for accurate single cell detection and proof of monoclonality at day 0. Streamline your workflow with comparative confluence assays to identify and verify gene edits.&lt;/p>\n&lt;ul>\n&lt;li>\n&lt;h4>Demonstrated IND success&lt;/h4>\n&lt;p>The Monoclonality Report feature streamlines the creation of supporting documentation for regulatory agencies. Reports are automatically generated based on parameters you select. The Monoclonality Report is an audit-ready document that supports filing for an Investigational New Drug (IND) Application with the FDA. (21 CFR Part 312)&lt;/p>\n&lt;/li>\n&lt;li>\n&lt;h4>Multichannel imaging and automated confluence&lt;/h4>\n&lt;p>Algorithms are optimized for accurate cell detection and address varying cell types and conditions. Publication-ready high-resolution imaging provides automatic confluence analysis and monoclonality assurance.&lt;/p>\n&lt;/li>\n&lt;li>\n&lt;h4>Rapid single cell confirmation&lt;/h4>\n&lt;p>The imager delivers industry leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence.&lt;/p>\n&lt;/li>\n&lt;/ul>\n&lt;p>&amp;nbsp;&lt;/p>\n&lt;h3>Features&lt;/h3>\n&lt;ul>\n&lt;li>\n&lt;h4>White light and fluorescent imaging&lt;/h4>\n&lt;p>Image every well in every plate with rapid acquisition times with label-free white light. Multichannel fluorescence imaging provides additional confidence of monoclonality and comparative confluence assays (red vs green).&lt;/p>\n&lt;/li>\n&lt;li>\n&lt;h4>Data tools to accelerate research timelines&lt;/h4>\n&lt;p>The software automatically calculates confluence measurements and generates growth curves, heatmaps, and image montages. Measurements for every well are automatically tracked over time. Streamline multiple steps (imaging, sample tracking, data analysis and report generation) in the cell line development workflow for IND filing.&lt;/p>\n&lt;/li>\n&lt;li>\n&lt;h4>Quickly image a variety of plate formats and cell types&lt;/h4>\n&lt;p>Image a 96-well plate in under two minutes. Compatible with adherent or settled suspension cell types such as CHO, HEK, hybridomas, iPSCs, and many other cell types.&lt;/p>\n&lt;/li>\n&lt;li>\n&lt;h4>Intelligent analysis with easy-to-use software&lt;/h4>\n&lt;p>The software automatically calculates confluence for each imaging time point. Growth curve, image montage, total growth, and mean rate are generated automatically and are exportable. Guided software user interface allows for simple 1-hour training.&lt;/p>\n&lt;/li>\n&lt;li>\n&lt;h4>High-resolution images&lt;/h4>\n&lt;p>High-speed fluorescence and high-resolution white light imaging with accurate detection of single cells including debris. Image visualization and data tracking over multiple days.&lt;/p>\n&lt;/li>\n&lt;li>\n&lt;h4>Custom automation options*&lt;/h4>\n&lt;p>The Automation and Customization Team offers a variety of custom services from robotic plate loading to fully automated workstations with liquid handling and incubation. We have built out custom automated work cells with the CloneSelect Imager for iPSC workflows, full assay systems and drug toxicity and characterization research.&lt;/p>\n&lt;p>&lt;em>*Price, time to deliver and specifications will vary based on mutually agreed technical requirements. Solution requirements may cause adjustment to standard performance.&lt;/em>&lt;/p>\n&lt;/li>\n&lt;/ul>&#34;,&#34;numresources&#34;:2,&#34;richdescription&#34;:&#34;&lt;h4>High-speed fluorescence and white light imaging, intelligent data analysis, and monoclonality report generation&lt;/h4>&#34;,&#34;obsolete&#34;:&#34;false&#34;,&#34;longdescription&#34;:&#34;Next-generation fluorescent imaging solution for the assurance of monoclonality and automated confluence across diverse cell types\nDemonstrating that cell lines are monoclonal – or that a gene was edited as expected – can be a time-consuming and highly-subjective process when relying on conventional technologies. The CloneSelect® Imager and CloneSelect® Imager FL are a high-throughput automated solutions for imaging and analyzing mammalian cells. Tracking the formation of a colony from a single cell is effortless as barcoded plates are tracked over time. Automated acquisition and analysis provides accurate, objective, and consistent results.\n\nWith high-resolution white light imaging, the CloneSelect Imager provides automated confluence, monoclonality assurance and industry leading acquisition times with the ability to image a 96-well plate in under two minutes.\n\nThe all new CloneSelect Imager FL features high contrast multichannel fluorescent and white light imaging that allows for accurate single cell detection and proof of monoclonality at day 0. Streamline your workflow with comparative confluence assays to identify and verify gene edits.\n\nDemonstrated IND success\nThe Monoclonality Report feature streamlines the creation of supporting documentation for regulatory agencies. Reports are automatically generated based on parameters you select. The Monoclonality Report is an audit-ready document that supports filing for an Investigational New Drug (IND) Application with the FDA. (21 CFR Part 312)\n\nMultichannel imaging and automated confluence\nAlgorithms are optimized for accurate cell detection and address varying cell types and conditions. Publication-ready high-resolution imaging provides automatic confluence analysis and monoclonality assurance.\n\nRapid single cell confirmation\nThe imager delivers industry leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence.\n\n\n\nFeatures\nWhite light and fluorescent imaging\nImage every well in every plate with rapid acquisition times with label-free white light. Multichannel fluorescence imaging provides additional confidence of monoclonality and comparative confluence assays (red vs green).\n\nData tools to accelerate research timelines\nThe software automatically calculates confluence measurements and generates growth curves, heatmaps, and image montages. Measurements for every well are automatically tracked over time. Streamline multiple steps (imaging, sample tracking, data analysis and report generation) in the cell line development workflow for IND filing.\n\nQuickly image a variety of plate formats and cell types\nImage a 96-well plate in under two minutes. Compatible with adherent or settled suspension cell types such as CHO, HEK, hybridomas, iPSCs, and many other cell types.\n\nIntelligent analysis with easy-to-use software\nThe software automatically calculates confluence for each imaging time point. Growth curve, image montage, total growth, and mean rate are generated automatically and are exportable. Guided software user interface allows for simple 1-hour training.\n\nHigh-resolution images\nHigh-speed fluorescence and high-resolution white light imaging with accurate detection of single cells including debris. Image visualization and data tracking over multiple days.\n\nCustom automation options*\nThe Automation and Customization Team offers a variety of custom services from robotic plate loading to fully automated workstations with liquid handling and incubation. We have built out custom automated work cells with the CloneSelect Imager for iPSC workflows, full assay systems and drug toxicity and characterization research.\n\n*Price, time to deliver and specifications will vary based on mutually agreed technical requirements. 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The CloneSelect\\u00ae Imager and CloneSelect\\u00ae Imager FL are a high-throughput automated solutions for imaging and analyzing mammalian cells. Tracking the formation of a colony from a single cell is effortless as barcoded plates are tracked over time. Automated acquisition and analysis provides accurate, objective, and consistent results.\\n\\nWith high-resolution white light imaging, the CloneSelect Imager provides automated confluence, monoclonality assurance and industry leading acquisition times with the ability to image a 96-well plate in under two minutes.\\n\\nThe all new CloneSelect Imager FL features high contrast multichannel fluorescent and white light imaging that allows for accurate single cell detection and proof of monoclonality at day 0. Streamline your workflow with comparative confluence assays to identify and verify gene edits.\\n\\nDemonstrated IND success\\nThe Monoclonality Report feature streamlines the creation of supporting documentation for regulatory agencies. Reports are automatically generated based on parameters you select. The Monoclonality Report is an audit-ready document that supports filing for an Investigational New Drug (IND) Application with the FDA. (21 CFR Part 312)\\n\\nMultichannel imaging and automated confluence\\nAlgorithms are optimized for accurate cell detection and address varying cell types and conditions. Publication-ready high-resolution imaging provides automatic confluence analysis and monoclonality assurance.\\n\\nRapid single cell confirmation\\nThe imager delivers industry leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence.\\n\\n\\n\\nFeatures\\nWhite light and fluorescent imaging\\nImage every well in every plate with rapid acquisition times with label-free white light. Multichannel fluorescence imaging provides additional confidence of monoclonality and comparative confluence assays (red vs green).\\n\\nData tools to accelerate research timelines\\nThe software automatically calculates confluence measurements and generates growth curves, heatmaps, and image montages. Measurements for every well are automatically tracked over time. Streamline multiple steps (imaging, sample tracking, data analysis and report generation) in the cell line development workflow for IND filing.\\n\\nQuickly image a variety of plate formats and cell types\\nImage a 96-well plate in under two minutes. Compatible with adherent or settled suspension cell types such as CHO, HEK, hybridomas, iPSCs, and many other cell types.\\n\\nIntelligent analysis with easy-to-use software\\nThe software automatically calculates confluence for each imaging time point. Growth curve, image montage, total growth, and mean rate are generated automatically and are exportable. Guided software user interface allows for simple 1-hour training.\\n\\nHigh-resolution images\\nHigh-speed fluorescence and high-resolution white light imaging with accurate detection of single cells including debris. Image visualization and data tracking over multiple days.\\n\\nCustom automation options*\\nThe Automation and Customization Team offers a variety of custom services from robotic plate loading to fully automated workstations with liquid handling and incubation. We have built out custom automated work cells with the CloneSelect Imager for iPSC workflows, full assay systems and drug toxicity and characterization research.\\n\\n*Price, time to deliver and specifications will vary based on mutually agreed technical requirements. Solution requirements may cause adjustment to standard performance.\&#34;], \&#34;metadescription\&#34;: [\&#34;\&#34;], \&#34;richdescription\&#34;: [\&#34;&lt;h4>High-speed fluorescence and white light imaging, intelligent data analysis, and monoclonality report generation&lt;/h4>\&#34;], \&#34;lastenrichmentdate\&#34;: [\&#34;2024-07-19 04:22:25.9600290\&#34;], \&#34;productfamilymodel\&#34;: [\&#34;Test Product Family Model\&#34;], \&#34;defaultcategoryname\&#34;: [\&#34;Single-Cell Imaging Systems\&#34;], \&#34;richlongdescription\&#34;: [\&#34;&lt;h3>Next-generation fluorescent imaging solution for the assurance of monoclonality and automated confluence across diverse cell types&lt;/h3>\\n&lt;p>Demonstrating that cell lines are monoclonal &amp;ndash; or that a gene was edited as expected &amp;ndash; can be a time-consuming and highly-subjective process when relying on conventional technologies. The CloneSelect&amp;reg; Imager and CloneSelect&amp;reg; Imager FL are a high-throughput automated solutions for imaging and analyzing mammalian cells. Tracking the formation of a colony from a single cell is effortless as barcoded plates are tracked over time. Automated acquisition and analysis provides accurate, objective, and consistent results.&lt;/p>\\n&lt;p>With high-resolution white light imaging, the CloneSelect Imager provides automated confluence, monoclonality assurance and industry leading acquisition times with the ability to image a 96-well plate in under two minutes.&lt;/p>\\n&lt;p>The all new CloneSelect Imager FL features high contrast multichannel fluorescent and white light imaging that allows for accurate single cell detection and proof of monoclonality at day 0. Streamline your workflow with comparative confluence assays to identify and verify gene edits.&lt;/p>\\n&lt;ul>\\n&lt;li>\\n&lt;h4>Demonstrated IND success&lt;/h4>\\n&lt;p>The Monoclonality Report feature streamlines the creation of supporting documentation for regulatory agencies. Reports are automatically generated based on parameters you select. The Monoclonality Report is an audit-ready document that supports filing for an Investigational New Drug (IND) Application with the FDA. (21 CFR Part 312)&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Multichannel imaging and automated confluence&lt;/h4>\\n&lt;p>Algorithms are optimized for accurate cell detection and address varying cell types and conditions. Publication-ready high-resolution imaging provides automatic confluence analysis and monoclonality assurance.&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Rapid single cell confirmation&lt;/h4>\\n&lt;p>The imager delivers industry leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence.&lt;/p>\\n&lt;/li>\\n&lt;/ul>\\n&lt;p>&amp;nbsp;&lt;/p>\\n&lt;h3>Features&lt;/h3>\\n&lt;ul>\\n&lt;li>\\n&lt;h4>White light and fluorescent imaging&lt;/h4>\\n&lt;p>Image every well in every plate with rapid acquisition times with label-free white light. Multichannel fluorescence imaging provides additional confidence of monoclonality and comparative confluence assays (red vs green).&lt;/p>\\n&lt;/li>\\n&lt;li>\\n&lt;h4>Data tools to accelerate research timelines&lt;/h4>\\n&lt;p>The software automatically calculates confluence measurements and generates growth curves, heatmaps, and image montages. 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Guided software user interface allows for simple 1-hour training.&lt;/p>\n&lt;/li>\n&lt;li>\n&lt;h4>High-resolution images&lt;/h4>\n&lt;p>High-speed fluorescence and high-resolution white light imaging with accurate detection of single cells including debris. Image visualization and data tracking over multiple days.&lt;/p>\n&lt;/li>\n&lt;li>\n&lt;h4>Custom automation options*&lt;/h4>\n&lt;p>The Automation and Customization Team offers a variety of custom services from robotic plate loading to fully automated workstations with liquid handling and incubation. We have built out custom automated work cells with the CloneSelect Imager for iPSC workflows, full assay systems and drug toxicity and characterization research.&lt;/p>\n&lt;p>&lt;em>*Price, time to deliver and specifications will vary based on mutually agreed technical requirements. 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Automated acquisition and analysis provides accurate, objective, and consistent results.\n\nWith high-resolution white light imaging, the CloneSelect Imager provides automated confluence, monoclonality assurance and industry leading acquisition times with the ability to image a 96-well plate in under two minutes.\n\nThe all new CloneSelect Imager FL features high contrast multichannel fluorescent and white light imaging that allows for accurate single cell detection and proof of monoclonality at day 0. Streamline your workflow with comparative confluence assays to identify and verify gene edits.\n\nDemonstrated IND success\nThe Monoclonality Report feature streamlines the creation of supporting documentation for regulatory agencies. Reports are automatically generated based on parameters you select. The Monoclonality Report is an audit-ready document that supports filing for an Investigational New Drug (IND) Application with the FDA. (21 CFR Part 312)\n\nMultichannel imaging and automated confluence\nAlgorithms are optimized for accurate cell detection and address varying cell types and conditions. Publication-ready high-resolution imaging provides automatic confluence analysis and monoclonality assurance.\n\nRapid single cell confirmation\nThe imager delivers industry leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence.\n\n\n\nFeatures\nWhite light and fluorescent imaging\nImage every well in every plate with rapid acquisition times with label-free white light. Multichannel fluorescence imaging provides additional confidence of monoclonality and comparative confluence assays (red vs green).\n\nData tools to accelerate research timelines\nThe software automatically calculates confluence measurements and generates growth curves, heatmaps, and image montages. Measurements for every well are automatically tracked over time. 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+</div>
+
+    
 
-	<featuresection-card card-image="/content/dam/danaher/system/icons/cog-check.svg" title="Rapid single-cell confirmation" description="The imager delivers industry-leading acquisition times, imaging a 96-well plate in as little as two minutes and can verify monoclonality from day zero with fluorescence. ">
-	</featuresection-card>
 </div>
 
 
@@ -487,17 +578,35 @@
 
     
     
-    <div class="heading">
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+    <div class="container-fullwidth">
+
+<fulllayout class="max-w-7xl mx-auto w-full">
+<div class="bg-white">
+    <div class="max-w-7xl mx-auto w-full px-2 sm:px-2 md:px-4 lg:px-4 xl:px-1 2xl:px-0">
+        <div>
+
+
 
 
     
     
+    <div class="text"><div data-cmp-data-layer="{&#34;text-06c2491714&#34;:{&#34;@type&#34;:&#34;danaher/components/content/marketing/text&#34;,&#34;repo:modifyDate&#34;:&#34;2023-03-22T22:42:54Z&#34;,&#34;xdm:text&#34;:&#34;&lt;p>&amp;nbsp;&lt;/p>\r\n&lt;p>&amp;nbsp;&lt;/p>\r\n&#34;}}" id="text-06c2491714" class="cmp-text href-text">
     
+        <p> </p>
+<p> </p>
+
+</div>
 
     
+
+</div>
+
+
     
     
+    <div class="heading">
+<heading alignment="center" heading="Highlights" headingsize="b24"></heading></div>
+
 
     
     
@@ -643,6 +752,33 @@
 
     
     
+    <div class="container-fullwidth">
+
+<fulllayout class="max-w-7xl mx-auto w-full">
+<div>
+    <div class="max-w-7xl mx-auto w-full px-2 sm:px-2 md:px-4 lg:px-4 xl:px-1 2xl:px-0">
+        <div>
+
+
+
+
+    
+    
+    <div class="text"><div data-cmp-data-layer="{&#34;text-91dd4f598e&#34;:{&#34;@type&#34;:&#34;danaher/components/content/marketing/text&#34;,&#34;repo:modifyDate&#34;:&#34;2023-03-29T19:06:14Z&#34;,&#34;xdm:text&#34;:&#34;&lt;p>&amp;nbsp;&lt;/p>\r\n&lt;p>&amp;nbsp;&lt;/p>\r\n&lt;p>&amp;nbsp;&lt;/p>\r\n&#34;}}" id="text-91dd4f598e" class="cmp-text href-text">
+    
+        <p> </p>
+<p> </p>
+<p> </p>
+
+</div>
+
+    
+
+</div>
+
+
+    
+    
     <div class="grid">
 
 <grid columns="2">
@@ -715,6 +851,18 @@
 
     
     
+    <div class="container-fullwidth">
+
+<fulllayout class="max-w-7xl mx-auto w-full">
+<div>
+    <div class="max-w-7xl mx-auto w-full px-2 sm:px-2 md:px-4 lg:px-4 xl:px-1 2xl:px-0">
+        <div>
+
+
+
+
+    
+    
     <div class="product-menu">
 
 
@@ -1212,6 +1360,30 @@
 </fulllayout></div>
 
 
+</div>
+    </div>
+  </div>
+</fulllayout></div>
+
+
+</div>
+    </div>
+  </div>
+</fulllayout></div>
+
+
+</div>
+    </div>
+  </div>
+</fulllayout></div>
+
+
+</div>
+    </div>
+  </div>
+</fulllayout></div>
+
+
 </template>
         <template v-slot:overview>
 
@@ -1398,93 +1570,94 @@
 </div>
 <div class="script">
 <div><div class="footer" style="content-visibility: auto">
-  <footer class="bg-danaherpurple-800" aria-labelledby="footer-heading">
+  <footer class="bg-danaherpurple-50" aria-labelledby="footer-heading">
     <p id="footer-heading" class="sr-only">Footer</p>
     <div class="max-w-7xl mx-auto py-12 px-6 sm:px-6 lg:py-16 lg:px-8">
       <div class="sm:grid sm:grid-cols-2 md:grid-cols-4 xl:gap-8">
         <div class="mt-12 md:mt-0">
-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Solutions</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Solutions</p>
           <ul role="list" class="mt-4 space-y-4">
             <li>
-              <a href="/us/en/solutions/mabs/cell-line-development.html" class="text-base text-white hover:text-danaherpurple-50 ">Cell Line Development</a>
+              <a href="/us/en/solutions/mabs/cell-line-development.html" class="text-base hover:text-danaherpurple-800 hover:underline">Cell Line Development</a>
             </li>
             <li>
-              <a href="/us/en/solutions/mrna-therapy.html" class="text-base text-white hover:text-danaherpurple-50 ">mRNA Development</a>
+              <a href="/us/en/solutions/mrna-therapy.html" class="text-base hover:text-danaherpurple-800 hover:underline">mRNA Development</a>
             </li>
             <li>
-              <a href="/us/en/solutions/oligonucleotide-therapy/antisense-oligonucleotide-development-manufacturing.html" class="text-base text-white hover:text-danaherpurple-50 ">Antisense Oligonucleotide</a>
+              <a href="/us/en/solutions/oligonucleotide-therapy/antisense-oligonucleotide-development-manufacturing.html" class="text-base hover:text-danaherpurple-800 hover:underline">Antisense Oligonucleotide</a>
             </li>
             <li>
-              <a href="/us/en/solutions/pdna-synthesis.html" class="text-base text-white hover:text-danaherpurple-50 ">pDNA Synthesis</a>
+              <a href="/us/en/solutions/pdna-synthesis.html" class="text-base hover:text-danaherpurple-800 hover:underline">pDNA Synthesis</a>
             </li>
             <li>
-              <a href="/us/en/solutions/cell-therapy.html" class="text-base text-white hover:text-danaherpurple-50 ">Cell Therapy</a>
+              <a href="/us/en/solutions/small-molecule-drug-discovery.html" class="text-base hover:text-danaherpurple-800 hover:underline">Small Molecules</a>
+            </li>            
+            <li>
+              <a href="/us/en/solutions/cell-therapy.html" class="text-base hover:text-danaherpurple-800 hover:underline">Cell Therapy</a>
             </li>
             <li>
-              <a href="/us/en/solutions/gene-therapy.html" class="text-base text-white hover:text-danaherpurple-50 ">Gene Therapy</a>
+              <a href="/us/en/solutions/gene-therapy.html" class="text-base hover:text-danaherpurple-800 hover:underline">Gene Therapy</a>
             </li>
           </ul>
         </div>
         <div class="mt-12 md:mt-0">
-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Explore</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Explore</p>
           <ul role="list" class="mt-4 space-y-4">
             <li>
-              <a href="/us/en/products.html" class="text-base text-white hover:text-danaherpurple-50">Products</a>
+              <a href="/us/en/products.html" class="text-base hover:text-danaherpurple-800 hover:underline">Products</a>
             </li>
             <li>
-              <a href="/us/en/solutions.html" class="text-base text-white hover:text-danaherpurple-50">Solutions</a>
+              <a href="/us/en/solutions.html" class="text-base hover:text-danaherpurple-800 hover:underline">Solutions</a>
             </li>
             <li>
-              <a href="/us/en/application.html" class="text-base text-white hover:text-danaherpurple-50">Applications</a>
+              <a href="/us/en/application.html" class="text-base hover:text-danaherpurple-800 hover:underline">Applications</a>
             </li>
             <li>
-              <a href="/us/en/library.html" class="text-base text-white hover:text-danaherpurple-50">Technical Library</a>
+              <a href="/us/en/library.html" class="text-base hover:text-danaherpurple-800 hover:underline">Technical Library</a>
             </li>
             <li>
-              <a href="/us/en/expert.html" class="text-base text-white hover:text-danaherpurple-50">Talk
+              <a href="/us/en/expert.html" class="text-base hover:text-danaherpurple-800 hover:underline">Talk
                 to an Expert</a>
             </li>
             <li>
-              <a href="/us/en/quote-cart.html" class="text-base text-white hover:text-danaherpurple-50">Request a Quote</a>
+              <a href="/us/en/quote-cart.html" class="text-base hover:text-danaherpurple-800 hover:underline">Request a Quote</a>
             </li>
           </ul>
         </div>
         <div class="mt-12 md:mt-0">
-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Company</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Company</p>
           <ul role="list" class="mt-4 space-y-4">
             <li>
-              <a href="/us/en/about-us.html" class="text-base text-white hover:text-danaherpurple-50">About</a>
+              <a href="/us/en/about-us.html" class="text-base hover:text-danaherpurple-800 hover:underline">About</a>
             </li>
             <li>
-              <a href="/us/en/news.html" class="text-base text-white hover:text-danaherpurple-50">News</a>
+              <a href="/us/en/news.html" class="text-base hover:text-danaherpurple-800 hover:underline">News</a>
             </li>
             <li>
-              <a href="/us/en/blog.html" class="text-base text-white hover:text-danaherpurple-50">Blog</a>
+              <a href="/us/en/blog.html" class="text-base hover:text-danaherpurple-800 hover:underline">Blog</a>
             </li>
             <li>
-              <a href="https://jobs.danaher.com/global/en?utm_source=dhls_website&utm_medium=referral&utm_content=footer" class="text-base text-white hover:text-danaherpurple-50">Careers</a>
+              <a href="https://jobs.danaher.com/global/en?utm_source=dhls_website&utm_medium=referral&utm_content=footer" class="text-base hover:text-danaherpurple-800 hover:underline">Careers</a>
             </li>
           </ul>
         </div>
         <div class="mt-12 md:mt-0">
-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Legal</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Legal</p>
           <ul role="list" class="mt-4 space-y-4">
             <li>
-              <a href="/us/en/legal/cookies.html" class="text-base text-white hover:text-danaherpurple-50 ">Cookie Policy</a>
+              <a href="/us/en/legal/cookies.html" class="text-base hover:text-danaherpurple-800 hover:underline">Cookie Policy</a>
             </li>
-
             <li>
-              <a href="/us/en/legal/ccpa.html" class="text-base text-white hover:text-danaherpurple-50">Do Not Sell or Share My Data</a>
+              <a href="/us/en/legal/ccpa.html" class="text-base hover:text-danaherpurple-800 hover:underline">Do Not Sell or Share My Data</a>
             </li>
             <li>
-              <a href="#" class="text-base text-white hover:text-danaherpurple-50 ot-sdk-show-settings">Manage Cookies</a>
+              <a href="#" class="text-base hover:text-danaherpurple-800 hover:underlineot-sdk-show-settings">Manage Cookies</a>
             </li>
- 
             <li>
-              <a href="/us/en/legal/privacy-policy.html" class="text-base text-white hover:text-danaherpurple-50">Privacy Policy</a>
+              <a href="/us/en/legal/privacy-policy.html" class="text-base hover:text-danaherpurple-800 hover:underline">Privacy Policy</a>
             </li>
             <li>
-              <a href="/us/en/legal/terms-of-use.html" class="text-base text-white hover:text-danaherpurple-50">Terms of Use</a>
+              <a href="/us/en/legal/terms-of-use.html" class="text-base hover:text-danaherpurple-800 hover:underline">Terms of Use</a>
             </li>
           </ul>
         </div>
@@ -1492,13 +1665,13 @@
 
       <div class="mt-8 border-t border-danaherpurple-500 pt-8 sm:mt-8 lg:mt-8 lg:flex lg:items-center lg:justify-between">
         <div>
-          <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe to our newsletter</h3>
-          <p class="mt-2 leading-6 text-base text-white">The latest news, articles, and resources, sent to your inbox
+          <h3 class="text-sm font-semibold tracking-wider uppercase">Subscribe to our newsletter</h3>
+          <p class="mt-2 leading-6 text-base">The latest news, articles, and resources, sent to your inbox
             weekly.</p>
         </div>
         <div class="mt-6 sm:flex sm:max-w-md lg:mt-0">
           <div class="mt-4 sm:ml-4 sm:mt-0 sm:flex-shrink-0">
-            <a href="/us/en/connect/newsletter.html" class="btn border-2 px-8 my-auto ml-auto btn-primary">Subscribe</a>
+            <a href="/us/en/connect/newsletter.html" class="btn border-2 px-8 my-auto ml-auto btn-outline-trending-brand">Subscribe</a>
           </div>
         </div>
       </div>
@@ -1507,41 +1680,15 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
         <div class="flex space-x-6 md:order-2">
           <a href="https://www.linkedin.com/company/danaher-life-sciences/" class="text-gray-500 hover:text-danaherpurple-50">
             <span class="sr-only">LinkedIn</span>
-            <svg xmlns="http://www.w3.org/2000/svg" width="24" height="24" viewBox="0 0 24 24" style="fill: white;"><path d="M4.98 3.5c0 1.381-1.11 2.5-2.48 2.5s-2.48-1.119-2.48-2.5c0-1.38 1.11-2.5 2.48-2.5s2.48 1.12 2.48 2.5zm.02 4.5h-5v16h5v-16zm7.982 0h-4.968v16h4.969v-8.399c0-4.67 6.029-5.052 6.029 0v8.399h4.988v-10.131c0-7.88-8.922-7.593-11.018-3.714v-2.155z"/></svg>
+            <svg xmlns="http://www.w3.org/2000/svg" width="24" height="24" viewBox="0 0 24 24"><path d="M4.98 3.5c0 1.381-1.11 2.5-2.48 2.5s-2.48-1.119-2.48-2.5c0-1.38 1.11-2.5 2.48-2.5s2.48 1.12 2.48 2.5zm.02 4.5h-5v16h5v-16zm7.982 0h-4.968v16h4.969v-8.399c0-4.67 6.029-5.052 6.029 0v8.399h4.988v-10.131c0-7.88-8.922-7.593-11.018-3.714v-2.155z"/></svg>
           </a>
         </div>
-        <p class="mt-8 text-base text-white md:mt-0 md:order-1"> © 2023 DH Life Sciences, LLC. All Rights Reserved.
+        <p class="mt-8 text-base md:mt-0 md:order-1"> © 2024 DH Life Sciences, LLC. All Rights Reserved.
         </p>
       </div>
     </div>
   </footer>
 </div></div>
-</div>
-<div class="script">
-<div><component :is="'script'">
-window.onload = function() {
-
-var anchors = document.getElementsByTagName("a");
-
-for (var i = 0; i < anchors.length; i++) {
-    anchors[i].href = anchors[i].href.replace("/content/danaher/ls", "")
-
-    if (anchors[i].href.includes("?") || anchors[i].href.includes("lifesciences.danaher.com") ) {
-
-    } else {
-        anchors[i].href = anchors[i].href.concat("?utm_source=dhls_website")
-    }
-}
-
-}
-</component >
-
-<component :is="'style'">
-    .btn.orange {
-        background-color: #dc6016;
-        color: white;
-    }
-</component ></div>
 </div>
 
         
@@ -1585,7 +1732,7 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
 
     
     
-<script src="/etc.clientlibs/core/wcm/components/commons/datalayer/v1/clientlibs/core.wcm.components.commons.datalayer.v1.lc-904d3c2f1e821ab45124d66de422b409-lc.min.js"></script>
+<script src="/etc.clientlibs/core/wcm/components/commons/datalayer/v1/clientlibs/core.wcm.components.commons.datalayer.v1.lc-70264651675213ed7f7cc5a02a00f621-lc.min.js"></script>
 
 
 
@@ -1595,14 +1742,14 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
         
     
 <script src="/etc.clientlibs/core/wcm/components/commons/site/clientlibs/container.lc-0a6aff292f5cc42142779cde92054524-lc.min.js"></script>
-<script src="/etc.clientlibs/danaher/clientlibs/clientlib-base.lc-d2ce98f15d18ed03c818947635149abb-lc.min.js"></script>
+<script src="/etc.clientlibs/danaher/clientlibs/clientlib-base.lc-2a85512656f79a4d72626fea0d606318-lc.min.js"></script>
 
 
 
 
     
 <script src="/etc.clientlibs/danaher/clientlibs/clientlib-dependencies.lc-d41d8cd98f00b204e9800998ecf8427e-lc.min.js"></script>
-<script src="/etc.clientlibs/danaher/clientlibs/clientlib-site.lc-7ba46db2b072016ab9ddfd178cec52ba-lc.min.js"></script>
+<script src="/etc.clientlibs/danaher/clientlibs/clientlib-site.lc-26d30872729a07b9af9948e2214046af-lc.min.js"></script>
 
 
 
@@ -1673,6 +1820,8 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
 
 </script>
 
+<script src="https://cdn.usefathom.com/script.js" data-site="KGTBOGMR" defer></script>
+
 
     
 </body>
diff --git a/tools/actions/convert/test/fixtures/product3-converted.html b/tools/actions/convert/test/fixtures/product3-converted.html
index 5963780ff..19adec201 100644
--- a/tools/actions/convert/test/fixtures/product3-converted.html
+++ b/tools/actions/convert/test/fixtures/product3-converted.html
@@ -54,7 +54,23 @@ <h2>No constraints - 4x more data with 100% correlation</h2>
       <div class="columns">
         <div>
           <div>
-            <p><a href="https://player.vimeo.com/video/809017220?h=c59cdbdab2&#x26;badge=0&#x26;autopause=0&#x26;player_id=0&#x26;app_id=58479">Video Player</a></p>
+            <table>
+              <thead>
+                <tr>
+                  <th>Video Player</th>
+                </tr>
+              </thead>
+              <tbody>
+                <tr>
+                  <td>
+                    <p>
+                      <img src="https://vimeo.com/api/oembed.json?url=https%3A//vimeo.com/vimeo.com/video/809017220,809017220" alt="">
+                    </p>
+                    <p><a href="https://player.vimeo.com/video/809017220?h=c59cdbdab2;badge=0;autopause=0;player%5C_id=0;app%5C_id=58479">https://player.vimeo.com/video/809017220?h=c59cdbdab2;badge=0;autopause=0;player\_id=0;app\_id=58479</a></p>
+                  </td>
+                </tr>
+              </tbody>
+            </table>
             <p>3D Cell Culture, 7d spheroid formation of U343 cells. tfLC3 EGFP and mRFP + DAPI + WGA Alexa680. Objective: 20x NA 0.70 DRY</p>
           </div>
           <div>
@@ -72,7 +88,7 @@ <h2>No constraints - Select the right modality in real time</h2>
       <div class="columns">
         <div>
           <div>
-            <h1>No constraints - Achieve physiological-like conditions thoughout your experiments</h1>
+            <h2>No constraints - Achieve physiological-like conditions thoughout your experiments</h2>
             <p>Live cell experiments require the cells to be in optimal shape. Typically, 2D and 3D cells in media require the temperature and the pH (via CO2) in the environment to be controlled. Stable nutrition and ion concentrations require the evaporation to be minimal. Some experiments even demand the O2 to be mimicked closer to physiological levels. Mica can provide the right conditions in the live cell configuration.</p>
             <ul>
               <li><strong>Mica is an incubator</strong>: The entire encapsulated inner sample space can be climate controlled (temperature, CO2 and humidity regulation) and offers ideal conditions for short and long-term live cell observation.</li>
@@ -82,7 +98,23 @@ <h1>No constraints - Achieve physiological-like conditions thoughout your experi
             </ul>
           </div>
           <div>
-            <p><a href="https://player.vimeo.com/video/809768643?h=0814b7152d&#x26;badge=0&#x26;autopause=0&#x26;player_id=0&#x26;app_id=58479">Video Player</a></p>
+            <table>
+              <thead>
+                <tr>
+                  <th>Video Player</th>
+                </tr>
+              </thead>
+              <tbody>
+                <tr>
+                  <td>
+                    <p>
+                      <img src="https://vimeo.com/api/oembed.json?url=https%3A//vimeo.com/vimeo.com/video/809768643,809768643" alt="">
+                    </p>
+                    <p><a href="https://player.vimeo.com/video/809768643?h=0814b7152d%5C&#x26;badge=0%5C&#x26;autopause=0%5C&#x26;player%5C_id=0%5C&#x26;app%5C_id=58479">https://player.vimeo.com/video/809768643?h=0814b7152d\&#x26;badge=0\&#x26;autopause=0\&#x26;player\_id=0\&#x26;app\_id=58479</a></p>
+                  </td>
+                </tr>
+              </tbody>
+            </table>
             <p>Formation of 3D spheroids from 1000 stably transfected MDCK MX1-GFP cells per well (left half) and 1000 U2OS cells per well (right half). Time-lapse acquisition over 60 hours, with 30-minute intervals. Green, GFP. Gray, integrated modulation contrast.</p>
           </div>
         </div>
@@ -139,7 +171,7 @@ <h2>The Microhub era is now!</h2>
       <div class="section-metadata">
         <div>
           <div>tabIcon</div>
-          <div>/content/dam/danaher/system/icons/Chart bar.svg</div>
+          <div>/content/dam/danaher/system/icons/Chart-bar.svg</div>
         </div>
         <div>
           <div>tabName</div>
@@ -187,7 +219,7 @@ <h2>The Microhub era is now!</h2>
       <div class="section-metadata">
         <div>
           <div>tabIcon</div>
-          <div>/content/dam/danaher/system/icons/Clipboard list.svg</div>
+          <div>/content/dam/danaher/system/icons/Clipboard-list.svg</div>
         </div>
         <div>
           <div>tabName</div>
@@ -215,15 +247,15 @@ <h2>The Microhub era is now!</h2>
         </div>
         <div>
           <div>creationDate</div>
-          <div>Fri, 21 Jul 2023 18:49:46 GMT</div>
+          <div>Fri, 10 May 2024 13:58:04 GMT</div>
         </div>
         <div>
           <div>updateDate</div>
-          <div>Thu, 21 Dec 2023 09:59:35 GMT</div>
+          <div>Fri, 19 Jul 2024 05:16:57 GMT</div>
         </div>
       </div>
     </div>
   </main>
   <footer></footer>
 </body>
-</html>
+</html>
\ No newline at end of file
diff --git a/tools/actions/convert/test/fixtures/product3.html b/tools/actions/convert/test/fixtures/product3.html
index 00b725162..8839b57bf 100644
--- a/tools/actions/convert/test/fixtures/product3.html
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Mica can provide the right conditions in the live cell configuration.\\n\\nMica is an incubator: the entire encapsulated inner sample space can be climate controlled (temperature, CO2 and humidity regulation) and offers ideal conditions for short and long-term live cell observation.\\nFrom dark to light: Mica also enables you to enjoy a brightly lit lab\\u2014freeing you from the constraints of sitting in a dark room for hours monitoring your experiment.\\nRadically simplified workflows\\nIntelligent automation and AI-supported analysis enables greater efficiency and a faster track to publication.\\n\\nReduce over 60% of process steps through system intelligence\\nReduce time and effort from sample to insight by simplifying your entire workflow\\nEnable 100% reproducibility and repeatability throughout your experiment\\nKey Applications\\nFluosync\\nImage Acquisition\\nMicrohubimaging\\nMultiplexing\\nSpatial Biology\\nWidefield Microscopy\\nFluorescence\\nLive Cell Imaging\\nConfocal Microscopy\\nImage Analysis\\nDAPI\\nCell Biology\\nCancer Research\\nOrganoids and 3D Cell Culture\\nModel Organisms in Research\\nNeuroscience\\nThe Microhub era is now!\\nExperience the future.\&#34;], \&#34;microscopegroup\&#34;: [\&#34;Light Microscope\&#34;], \&#34;microscopelaser\&#34;: [\&#34;Fixed Wave Length\&#34;], \&#34;microscopetypes\&#34;: [\&#34;Inverted Microscope\&#34;, \&#34;Inverted Microscope\&#34;, \&#34;Digital Microscope\&#34;], \&#34;richdescription\&#34;: [\&#34;&lt;h4>This changes everything.&lt;/h4>\\n&lt;p>More than a highly automated microscope,&amp;nbsp;&lt;a>Mica&lt;/a>&amp;nbsp;unites widefield and confocal imaging in a sample protecting, incubating environment. With the simple push of a button, you have everything you need - all in one place - to supercharge fluorescence imaging workflows and get meaningful scientific results faster.&lt;/p>\\n&lt;p>Now you can focus on your science, not figuring out your microscope.&lt;/p>\\n&lt;ul>\\n&lt;li>Access for all\\n&lt;p>Mica provides a clear sample overview and allows to easily change observation conditions with just a few clicks&lt;/p>\\n&lt;/li>\\n&lt;li>No constraints\\n&lt;p>4x more data with 100% correlation. Select the right modality in real time. Achieve physiological-like conditions thoughout your experiments&lt;/p>\\n&lt;/li>\\n&lt;li>Radically simplified workflows\\n&lt;p>Intelligent automation and AI-supported analysis enables greater efficiency and a faster track to publication&lt;/p>\\n&lt;/li>\\n&lt;/ul>\&#34;], \&#34;numspecifications\&#34;: [13], \&#34;contrastingmethods\&#34;: [\&#34;Brightfield\&#34;, \&#34;Fluorescence\&#34;, \&#34;Integrated Modulation Contrast\&#34;], \&#34;specificationsjson\&#34;: [\&#34;{}\&#34;], \&#34;defaultcategoryname\&#34;: [\&#34;Digital Microscopes\&#34;], \&#34;hasresonancescanner\&#34;: [\&#34;No\&#34;], \&#34;microscopytechnique\&#34;: [\&#34;Confocal Microscopy\&#34;], \&#34;richlongdescription\&#34;: [\&#34;&lt;h2>The world&amp;rsquo;s first imaging Microhub. Mica&lt;/h2>\\n&lt;h3>Access for all&lt;/h3>\\n&lt;p>Everyone can now leverage microscopy to make more discoveries.&lt;/p>\\n&lt;p>&lt;a>Mica&lt;/a> provides a clear sample overview and allows to easily change observation conditions with just a few clicks.&lt;/p>\\n&lt;ul>\\n&lt;li>85% fewer steps to the first image&lt;/li>\\n&lt;li>33% less time to the first image&lt;/li>\\n&lt;li>50% of the training time&lt;/li>\\n&lt;/ul>\\n&lt;h3>No constraints - 4x more data with 100% correlation&lt;/h3>\\n&lt;p>The Microhub enables you to simultaneously capture all 4 labels of different structures in a single acquisition for widefield or confocal, without ever moving your sample. This overcomes the spatiotemporal mismatch between labels of moving objects during sequential acquisition. All powered by our patented FluoSync technology, a fast and gentle method for multicolor fluorescence imaging.&lt;/p>\\n&lt;p>&lt;a>Read the whitepaper on FluoSync&lt;/a>&lt;/p>\\n&lt;h3>No constraints - Select the right modality in real time&lt;/h3>\\n&lt;p>&lt;a>Mica&lt;/a> unifies transmitted and fluorescence light imaging modalities. You can select from multiple imaging modalities all within one Microhub, including widefield, confocal, THUNDER imaging, LIGHTNING, Z-stacks, time-lapse and more.&lt;/p>\\n&lt;p>This enables you to&lt;/p>\\n&lt;ul>\\n&lt;li>generate fast overviews with widefield at low magnification&lt;/li>\\n&lt;li>gradually zoom in on the regions of interest&lt;/li>\\n&lt;li>switch to confocal when and where needed without ever moving the sample to a different system&lt;/li>\\n&lt;/ul>\\n&lt;h3>No constraints - Achieve physiological-like conditions thoughout your experiments&lt;/h3>\\n&lt;p>Live cell experiments require the cells to be in optimal shape. Typically, 2D and 3D cells in media require the temperature and the pH (via CO2) in the environment to be controlled. Stable nutrition and ion concentrations require the evaporation to be minimal. Some experiments even demand the O2 to be mimicked closer to physiological levels. Mica can provide the right conditions in the live cell configuration.&lt;/p>\\n&lt;ul>\\n&lt;li>&lt;a>Mica&lt;/a> is an incubator: the entire encapsulated inner sample space can be climate controlled (temperature, CO2 and humidity regulation) and offers ideal conditions for short and long-term live cell observation.&lt;/li>\\n&lt;li>From dark to light: &lt;a>Mica&lt;/a> also enables you to enjoy a brightly lit lab&amp;mdash;freeing you from the constraints of sitting in a dark room for hours monitoring your experiment.&lt;/li>\\n&lt;/ul>\\n&lt;h3>Radically simplified workflows&lt;/h3>\\n&lt;p>Intelligent automation and AI-supported analysis enables greater efficiency and a faster track to publication.&lt;/p>\\n&lt;ul>\\n&lt;li>Reduce over 60% of process steps through system intelligence&lt;/li>\\n&lt;li>Reduce time and effort from sample to insight by simplifying your entire workflow&lt;/li>\\n&lt;li>Enable 100% reproducibility and repeatability throughout your experiment&lt;/li>\\n&lt;/ul>\\n&lt;h3>Key Applications&lt;/h3>\\n&lt;ul>\\n&lt;li>Fluosync&lt;/li>\\n&lt;li>Image Acquisition&lt;/li>\\n&lt;li>Microhubimaging&lt;/li>\\n&lt;li>Multiplexing&lt;/li>\\n&lt;li>Spatial Biology&lt;/li>\\n&lt;li>Widefield Microscopy&lt;/li>\\n&lt;li>Fluorescence&lt;/li>\\n&lt;li>Live Cell Imaging&lt;/li>\\n&lt;li>Confocal Microscopy&lt;/li>\\n&lt;li>Image Analysis&lt;/li>\\n&lt;li>DAPI&lt;/li>\\n&lt;li>Cell Biology&lt;/li>\\n&lt;li>Cancer Research&lt;/li>\\n&lt;li>Organoids and 3D Cell Culture&lt;/li>\\n&lt;li>Model Organisms in Research&lt;/li>\\n&lt;li>Neuroscience&lt;/li>\\n&lt;/ul>\\n&lt;h3>The Microhub era is now!&lt;/h3>\\n&lt;p>Experience the future.&lt;/p>\&#34;], \&#34;microscopestagetypes\&#34;: [\&#34;Motorized\&#34;], \&#34;microscopecameraoptions\&#34;: [\&#34;Integrated\&#34;], \&#34;microscopysoftwareavailable\&#34;: [\&#34;2D Anaylsis\&#34;, \&#34;3D Acquisition (Z-Stacking)\&#34;, \&#34;3D Analysis\&#34;, \&#34;Deconvolution\&#34;, \&#34;Documentation\&#34;, \&#34;Live Cell Imaging\&#34;, \&#34;Multichannel Acquisition\&#34;, \&#34;Multiposition Acquisition\&#34;, \&#34;Super Resolution\&#34;, \&#34;Tile Stitching\&#34;, \&#34;Time Lapse Imaging\&#34;], \&#34;microscopeenvironmentalcontrol\&#34;: [\&#34;Box\&#34;]}}, {\&#34;Origin\&#34;: \&#34;field decomposition\&#34;, \&#34;Values\&#34;: {\&#34;decomposed_sku\&#34;: [\&#34;mic\&#34;, \&#34;mica\&#34;], \&#34;decomposed_productid\&#34;: [\&#34;mic\&#34;, \&#34;mica\&#34;]}}, {\&#34;Origin\&#34;: \&#34;view all metadata\&#34;, \&#34;Values\&#34;: {}}]&#34;,&#34;richlongdescription&#34;:&#34;&lt;h2>The world&amp;rsquo;s first imaging Microhub. Mica&lt;/h2>\n&lt;h3>Access for all&lt;/h3>\n&lt;p>Everyone can now leverage microscopy to make more discoveries.&lt;/p>\n&lt;p>&lt;a>Mica&lt;/a> provides a clear sample overview and allows to easily change observation conditions with just a few clicks.&lt;/p>\n&lt;ul>\n&lt;li>85% fewer steps to the first image&lt;/li>\n&lt;li>33% less time to the first image&lt;/li>\n&lt;li>50% of the training time&lt;/li>\n&lt;/ul>\n&lt;h3>No constraints - 4x more data with 100% correlation&lt;/h3>\n&lt;p>The Microhub enables you to simultaneously capture all 4 labels of different structures in a single acquisition for widefield or confocal, without ever moving your sample. This overcomes the spatiotemporal mismatch between labels of moving objects during sequential acquisition. All powered by our patented FluoSync technology, a fast and gentle method for multicolor fluorescence imaging.&lt;/p>\n&lt;p>&lt;a>Read the whitepaper on FluoSync&lt;/a>&lt;/p>\n&lt;h3>No constraints - Select the right modality in real time&lt;/h3>\n&lt;p>&lt;a>Mica&lt;/a> unifies transmitted and fluorescence light imaging modalities. You can select from multiple imaging modalities all within one Microhub, including widefield, confocal, THUNDER imaging, LIGHTNING, Z-stacks, time-lapse and more.&lt;/p>\n&lt;p>This enables you to&lt;/p>\n&lt;ul>\n&lt;li>generate fast overviews with widefield at low magnification&lt;/li>\n&lt;li>gradually zoom in on the regions of interest&lt;/li>\n&lt;li>switch to confocal when and where needed without ever moving the sample to a different system&lt;/li>\n&lt;/ul>\n&lt;h3>No constraints - Achieve physiological-like conditions thoughout your experiments&lt;/h3>\n&lt;p>Live cell experiments require the cells to be in optimal shape. Typically, 2D and 3D cells in media require the temperature and the pH (via CO2) in the environment to be controlled. Stable nutrition and ion concentrations require the evaporation to be minimal. Some experiments even demand the O2 to be mimicked closer to physiological levels. Mica can provide the right conditions in the live cell configuration.&lt;/p>\n&lt;ul>\n&lt;li>&lt;a>Mica&lt;/a> is an incubator: the entire encapsulated inner sample space can be climate controlled (temperature, CO2 and humidity regulation) and offers ideal conditions for short and long-term live cell observation.&lt;/li>\n&lt;li>From dark to light: &lt;a>Mica&lt;/a> also enables you to enjoy a brightly lit lab&amp;mdash;freeing you from the constraints of sitting in a dark room for hours monitoring your experiment.&lt;/li>\n&lt;/ul>\n&lt;h3>Radically simplified workflows&lt;/h3>\n&lt;p>Intelligent automation and AI-supported analysis enables greater efficiency and a faster track to publication.&lt;/p>\n&lt;ul>\n&lt;li>Reduce over 60% of process steps through system intelligence&lt;/li>\n&lt;li>Reduce time and effort from sample to insight by simplifying your entire workflow&lt;/li>\n&lt;li>Enable 100% reproducibility and repeatability throughout your experiment&lt;/li>\n&lt;/ul>\n&lt;h3>Key Applications&lt;/h3>\n&lt;ul>\n&lt;li>Fluosync&lt;/li>\n&lt;li>Image Acquisition&lt;/li>\n&lt;li>Microhubimaging&lt;/li>\n&lt;li>Multiplexing&lt;/li>\n&lt;li>Spatial Biology&lt;/li>\n&lt;li>Widefield Microscopy&lt;/li>\n&lt;li>Fluorescence&lt;/li>\n&lt;li>Live Cell Imaging&lt;/li>\n&lt;li>Confocal Microscopy&lt;/li>\n&lt;li>Image Analysis&lt;/li>\n&lt;li>DAPI&lt;/li>\n&lt;li>Cell Biology&lt;/li>\n&lt;li>Cancer Research&lt;/li>\n&lt;li>Organoids and 3D Cell Culture&lt;/li>\n&lt;li>Model Organisms in Research&lt;/li>\n&lt;li>Neuroscience&lt;/li>\n&lt;/ul>\n&lt;h3>The Microhub era is now!&lt;/h3>\n&lt;p>Experience the future.&lt;/p>&#34;,&#34;numresources&#34;:2,&#34;microscopeenvironmentalcontrol&#34;:&#34;Box&#34;,&#34;richdescription&#34;:&#34;&lt;h4>This changes everything.&lt;/h4>\n&lt;p>More than a highly automated microscope,&amp;nbsp;&lt;a>Mica&lt;/a>&amp;nbsp;unites widefield and confocal imaging in a sample protecting, incubating environment. With the simple push of a button, you have everything you need - all in one place - to supercharge fluorescence imaging workflows and get meaningful scientific results faster.&lt;/p>\n&lt;p>Now you can focus on your science, not figuring out your microscope.&lt;/p>\n&lt;ul>\n&lt;li>Access for all\n&lt;p>Mica provides a clear sample overview and allows to easily change observation conditions with just a few clicks&lt;/p>\n&lt;/li>\n&lt;li>No constraints\n&lt;p>4x more data with 100% correlation. Select the right modality in real time. Achieve physiological-like conditions thoughout your experiments&lt;/p>\n&lt;/li>\n&lt;li>Radically simplified workflows\n&lt;p>Intelligent automation and AI-supported analysis enables greater efficiency and a faster track to publication&lt;/p>\n&lt;/li>\n&lt;/ul>&#34;,&#34;obsolete&#34;:&#34;false&#34;,&#34;longdescription&#34;:&#34;The world’s first imaging Microhub. Mica\nThis changes everything.\nMore than a highly automated microscope, Mica unites widefield and confocal imaging in a sample protecting, incubating environment. With the simple push of a button, you have everything you need - all in one place - to supercharge fluorescence imaging workflows and get meaningful scientific results faster.\n\nNow you can focus on your science, not figuring out your microscope.\n\nAccess for all\nNo constraints\nRadically simplified workflows\nAccess for all\nEveryone can now leverage microscopy to make more discoveries.\n\nMica provides a clear sample overview and allows to easily change observation conditions with just a few clicks.\n\n85% fewer steps to the first image\n33% less time to the first image\n50% of the training time\nNo constraints - 4x more data with 100% correlation\nThe Microhub enables you to simultaneously capture all 4 labels of different structures in a single acquisition for widefield or confocal, without ever moving your sample. This overcomes the spatiotemporal mismatch between labels of moving objects during sequential acquisition. All powered by our patented FluoSync technology, a fast and gentle method for multicolor fluorescence imaging.\n\nRead the whitepaper on FluoSync\n\nNo constraints - Select the right modality in real time\nMica unifies transmitted and fluorescence light imaging modalities. You can select from multiple imaging modalities all within one Microhub, including widefield, confocal, THUNDER imaging, LIGHTNING, Z-stacks, time-lapse and more.\n\nThis enables you to\n\ngenerate fast overviews with widefield at low magnification\ngradually zoom in on the regions of interest\nswitch to confocal when and where needed without ever moving the sample to a different system\nNo constraints - Achieve physiological-like conditions thoughout your experiments\nLive cell experiments require the cells to be in optimal shape. Typically, 2D and 3D cells in media require the temperature and the pH (via CO2) in the environment to be controlled. Stable nutrition and ion concentrations require the evaporation to be minimal. Some experiments even demand the O2 to be mimicked closer to physiological levels. 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Mica\nThis changes everything.\nMore than a highly automated microscope, Mica unites widefield and confocal imaging in a sample protecting, incubating environment. With the simple push of a button, you have everything you need - all in one place - to supercharge fluorescence imaging workflows and get meaningful scientific results faster.\n\nNow you can focus on your science, not figuring out your microscope.\n\nAccess for all\nNo constraints\nRadically simplified workflows\nAccess for all\nEveryone can now leverage microscopy to make more discoveries.\n\nMica provides a clear sample overview and allows to easily change observation conditions with just a few clicks.\n\n85% fewer steps to the first image\n33% less time to the first image\n50% of the training time\nNo constraints - 4x more data with 100% correlation\nThe Microhub enables you to simultaneously capture all 4 labels of different structures in a single acquisition for widefield or confocal, without ever moving your sample. This overcomes the spatiotemporal mismatch between labels of moving objects during sequential acquisition. All powered by our patented FluoSync technology, a fast and gentle method for multicolor fluorescence imaging.\n\nRead the whitepaper on FluoSync\n\nNo constraints - Select the right modality in real time\nMica unifies transmitted and fluorescence light imaging modalities. You can select from multiple imaging modalities all within one Microhub, including widefield, confocal, THUNDER imaging, LIGHTNING, Z-stacks, time-lapse and more.\n\nThis enables you to\n\ngenerate fast overviews with widefield at low magnification\ngradually zoom in on the regions of interest\nswitch to confocal when and where needed without ever moving the sample to a different system\nNo constraints - Achieve physiological-like conditions thoughout your experiments\nLive cell experiments require the cells to be in optimal shape. 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Mica&lt;/h2>\n&lt;h3>Access for all&lt;/h3>\n&lt;p>Everyone can now leverage microscopy to make more discoveries.&lt;/p>\n&lt;p>&lt;a>Mica&lt;/a> provides a clear sample overview and allows to easily change observation conditions with just a few clicks.&lt;/p>\n&lt;ul>\n&lt;li>85% fewer steps to the first image&lt;/li>\n&lt;li>33% less time to the first image&lt;/li>\n&lt;li>50% of the training time&lt;/li>\n&lt;/ul>\n&lt;h3>No constraints - 4x more data with 100% correlation&lt;/h3>\n&lt;p>The Microhub enables you to simultaneously capture all 4 labels of different structures in a single acquisition for widefield or confocal, without ever moving your sample. This overcomes the spatiotemporal mismatch between labels of moving objects during sequential acquisition. All powered by our patented FluoSync technology, a fast and gentle method for multicolor fluorescence imaging.&lt;/p>\n&lt;p>&lt;a>Read the whitepaper on FluoSync&lt;/a>&lt;/p>\n&lt;h3>No constraints - Select the right modality in real time&lt;/h3>\n&lt;p>&lt;a>Mica&lt;/a> unifies transmitted and fluorescence light imaging modalities. You can select from multiple imaging modalities all within one Microhub, including widefield, confocal, THUNDER imaging, LIGHTNING, Z-stacks, time-lapse and more.&lt;/p>\n&lt;p>This enables you to&lt;/p>\n&lt;ul>\n&lt;li>generate fast overviews with widefield at low magnification&lt;/li>\n&lt;li>gradually zoom in on the regions of interest&lt;/li>\n&lt;li>switch to confocal when and where needed without ever moving the sample to a different system&lt;/li>\n&lt;/ul>\n&lt;h3>No constraints - Achieve physiological-like conditions thoughout your experiments&lt;/h3>\n&lt;p>Live cell experiments require the cells to be in optimal shape. 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With the simple push of a button, you have everything you need - all in one place - to supercharge fluorescence imaging workflows and get meaningful scientific results faster.&lt;/p>\n&lt;p>Now you can focus on your science, not figuring out your microscope.&lt;/p>\n&lt;ul>\n&lt;li>Access for all\n&lt;p>Mica provides a clear sample overview and allows to easily change observation conditions with just a few clicks&lt;/p>\n&lt;/li>\n&lt;li>No constraints\n&lt;p>4x more data with 100% correlation. Select the right modality in real time. Achieve physiological-like conditions thoughout your experiments&lt;/p>\n&lt;/li>\n&lt;li>Radically simplified workflows\n&lt;p>Intelligent automation and AI-supported analysis enables greater efficiency and a faster track to publication&lt;/p>\n&lt;/li>\n&lt;/ul>&#34;,&#34;obsolete&#34;:&#34;false&#34;,&#34;longdescription&#34;:&#34;The world’s first imaging Microhub. 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This overcomes the spatiotemporal mismatch between labels of moving objects during sequential acquisition. All powered by our patented FluoSync technology, a fast and gentle method for multicolor fluorescence imaging.\n\nRead the whitepaper on FluoSync\n\nNo constraints - Select the right modality in real time\nMica unifies transmitted and fluorescence light imaging modalities. You can select from multiple imaging modalities all within one Microhub, including widefield, confocal, THUNDER imaging, LIGHTNING, Z-stacks, time-lapse and more.\n\nThis enables you to\n\ngenerate fast overviews with widefield at low magnification\ngradually zoom in on the regions of interest\nswitch to confocal when and where needed without ever moving the sample to a different system\nNo constraints - Achieve physiological-like conditions thoughout your experiments\nLive cell experiments require the cells to be in optimal shape. 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+<div><div style="padding:100% 0 0 0;position:relative;"><iframe src="https://player.vimeo.com/video/809017220?h=c59cdbdab2;badge=0;autopause=0;player_id=0;app_id=58479" frameborder="0" allow="autoplay; fullscreen; picture-in-picture" allowfullscreen style="position:absolute;top:0;left:0;width:100%;height:100%;" title="lms-mica-spheroids-4_10"></iframe></div></div>
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+    <feature-image textwidth="w-3/4" title="No constraints - Select the right modality in real time" titlesize="xxxl" description="&lt;p>Mica unifies transmitted and fluorescence light imaging modalities. You can&amp;nbsp;select from multiple imaging modalities all within one Microhub, including widefield, confocal, THUNDER imaging, LIGHTNING, Z-stacks, time-lapse and more.&lt;/p>
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+    <feature-image textwidth="_self" title="No constraints - Achieve physiological-like conditions thoughout your experiments" titlesize="xxxl" description="&lt;p>Live cell experiments require the cells to be in optimal shape. Typically, 2D and 3D cells in media require the temperature and the pH (via CO2) in the environment to be controlled. Stable nutrition and ion concentrations require the evaporation to be minimal. Some experiments even demand the O2 to be mimicked closer to physiological levels. Mica can provide the right conditions in the live cell configuration. &lt;/p>
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+&lt;ul>
+&lt;li>&lt;b>Mica is an incubator&lt;/b>: The entire encapsulated inner sample space can be climate controlled (temperature, CO2 and humidity regulation) and offers ideal conditions for short and long-term live cell observation.&lt;/li>
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+&lt;ul>
+&lt;li>&lt;b>From dark to light&lt;/b>: Mica also enables you to enjoy a brightly lit lab—freeing you from the constraints of sitting in a dark room for hours monitoring your experiment.&lt;/li>
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+    <div class="text"><div data-cmp-data-layer="{&#34;text-d461b05208&#34;:{&#34;@type&#34;:&#34;danaher/components/content/marketing/text&#34;,&#34;repo:modifyDate&#34;:&#34;2023-03-23T00:14:09Z&#34;,&#34;xdm:text&#34;:&#34;&lt;p>&lt;span style=\&#34;color: #AAAAAA;\&#34;>U2OS cells were labelled with SiR-Actin, TMRE (mitochondria activity), CellEvent™ (caspase activity), and DAPI (nuclei). 63x magnification, widefield mode.&lt;/span>&lt;/p>\r\n&#34;}}" id="text-d461b05208" class="cmp-text href-text">
     
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+              <a href="/us/en/solutions/small-molecule-drug-discovery.html" class="text-base hover:text-danaherpurple-800 hover:underline">Small Molecules</a>
+            </li>            
+            <li>
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-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Explore</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Explore</p>
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-              <a href="/us/en/products.html" class="text-base text-white hover:text-danaherpurple-50">Products</a>
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             <li>
-              <a href="/us/en/expert.html" class="text-base text-white hover:text-danaherpurple-50">Talk
+              <a href="/us/en/expert.html" class="text-base hover:text-danaherpurple-800 hover:underline">Talk
                 to an Expert</a>
             </li>
             <li>
-              <a href="/us/en/quote-cart.html" class="text-base text-white hover:text-danaherpurple-50">Request a Quote</a>
+              <a href="/us/en/quote-cart.html" class="text-base hover:text-danaherpurple-800 hover:underline">Request a Quote</a>
             </li>
           </ul>
         </div>
         <div class="mt-12 md:mt-0">
-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Company</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Company</p>
           <ul role="list" class="mt-4 space-y-4">
             <li>
-              <a href="/us/en/about-us.html" class="text-base text-white hover:text-danaherpurple-50">About</a>
+              <a href="/us/en/about-us.html" class="text-base hover:text-danaherpurple-800 hover:underline">About</a>
             </li>
             <li>
-              <a href="/us/en/news.html" class="text-base text-white hover:text-danaherpurple-50">News</a>
+              <a href="/us/en/news.html" class="text-base hover:text-danaherpurple-800 hover:underline">News</a>
             </li>
             <li>
-              <a href="/us/en/blog.html" class="text-base text-white hover:text-danaherpurple-50">Blog</a>
+              <a href="/us/en/blog.html" class="text-base hover:text-danaherpurple-800 hover:underline">Blog</a>
             </li>
             <li>
-              <a href="https://jobs.danaher.com/global/en?utm_source=dhls_website&utm_medium=referral&utm_content=footer" class="text-base text-white hover:text-danaherpurple-50">Careers</a>
+              <a href="https://jobs.danaher.com/global/en?utm_source=dhls_website&utm_medium=referral&utm_content=footer" class="text-base hover:text-danaherpurple-800 hover:underline">Careers</a>
             </li>
           </ul>
         </div>
         <div class="mt-12 md:mt-0">
-          <p class="text-sm font-semibold text-white tracking-wider uppercase">Legal</p>
+          <p class="text-sm font-semibold tracking-wider uppercase">Legal</p>
           <ul role="list" class="mt-4 space-y-4">
             <li>
-              <a href="/us/en/legal/cookies.html" class="text-base text-white hover:text-danaherpurple-50 ">Cookie Policy</a>
+              <a href="/us/en/legal/cookies.html" class="text-base hover:text-danaherpurple-800 hover:underline">Cookie Policy</a>
             </li>
-
             <li>
-              <a href="/us/en/legal/ccpa.html" class="text-base text-white hover:text-danaherpurple-50">Do Not Sell or Share My Data</a>
+              <a href="/us/en/legal/ccpa.html" class="text-base hover:text-danaherpurple-800 hover:underline">Do Not Sell or Share My Data</a>
             </li>
             <li>
-              <a href="#" class="text-base text-white hover:text-danaherpurple-50 ot-sdk-show-settings">Manage Cookies</a>
+              <a href="#" class="text-base hover:text-danaherpurple-800 hover:underlineot-sdk-show-settings">Manage Cookies</a>
             </li>
- 
             <li>
-              <a href="/us/en/legal/privacy-policy.html" class="text-base text-white hover:text-danaherpurple-50">Privacy Policy</a>
+              <a href="/us/en/legal/privacy-policy.html" class="text-base hover:text-danaherpurple-800 hover:underline">Privacy Policy</a>
             </li>
             <li>
-              <a href="/us/en/legal/terms-of-use.html" class="text-base text-white hover:text-danaherpurple-50">Terms of Use</a>
+              <a href="/us/en/legal/terms-of-use.html" class="text-base hover:text-danaherpurple-800 hover:underline">Terms of Use</a>
             </li>
           </ul>
         </div>
@@ -1319,13 +1216,13 @@
 
       <div class="mt-8 border-t border-danaherpurple-500 pt-8 sm:mt-8 lg:mt-8 lg:flex lg:items-center lg:justify-between">
         <div>
-          <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe to our newsletter</h3>
-          <p class="mt-2 leading-6 text-base text-white">The latest news, articles, and resources, sent to your inbox
+          <h3 class="text-sm font-semibold tracking-wider uppercase">Subscribe to our newsletter</h3>
+          <p class="mt-2 leading-6 text-base">The latest news, articles, and resources, sent to your inbox
             weekly.</p>
         </div>
         <div class="mt-6 sm:flex sm:max-w-md lg:mt-0">
           <div class="mt-4 sm:ml-4 sm:mt-0 sm:flex-shrink-0">
-            <a href="/us/en/connect/newsletter.html" class="btn border-2 px-8 my-auto ml-auto btn-primary">Subscribe</a>
+            <a href="/us/en/connect/newsletter.html" class="btn border-2 px-8 my-auto ml-auto btn-outline-trending-brand">Subscribe</a>
           </div>
         </div>
       </div>
@@ -1334,41 +1231,15 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
         <div class="flex space-x-6 md:order-2">
           <a href="https://www.linkedin.com/company/danaher-life-sciences/" class="text-gray-500 hover:text-danaherpurple-50">
             <span class="sr-only">LinkedIn</span>
-            <svg xmlns="http://www.w3.org/2000/svg" width="24" height="24" viewBox="0 0 24 24" style="fill: white;"><path d="M4.98 3.5c0 1.381-1.11 2.5-2.48 2.5s-2.48-1.119-2.48-2.5c0-1.38 1.11-2.5 2.48-2.5s2.48 1.12 2.48 2.5zm.02 4.5h-5v16h5v-16zm7.982 0h-4.968v16h4.969v-8.399c0-4.67 6.029-5.052 6.029 0v8.399h4.988v-10.131c0-7.88-8.922-7.593-11.018-3.714v-2.155z"/></svg>
+            <svg xmlns="http://www.w3.org/2000/svg" width="24" height="24" viewBox="0 0 24 24"><path d="M4.98 3.5c0 1.381-1.11 2.5-2.48 2.5s-2.48-1.119-2.48-2.5c0-1.38 1.11-2.5 2.48-2.5s2.48 1.12 2.48 2.5zm.02 4.5h-5v16h5v-16zm7.982 0h-4.968v16h4.969v-8.399c0-4.67 6.029-5.052 6.029 0v8.399h4.988v-10.131c0-7.88-8.922-7.593-11.018-3.714v-2.155z"/></svg>
           </a>
         </div>
-        <p class="mt-8 text-base text-white md:mt-0 md:order-1"> © 2023 DH Life Sciences, LLC. All Rights Reserved.
+        <p class="mt-8 text-base md:mt-0 md:order-1"> © 2024 DH Life Sciences, LLC. All Rights Reserved.
         </p>
       </div>
     </div>
   </footer>
 </div></div>
-</div>
-<div class="script">
-<div><component :is="'script'">
-window.onload = function() {
-
-var anchors = document.getElementsByTagName("a");
-
-for (var i = 0; i < anchors.length; i++) {
-    anchors[i].href = anchors[i].href.replace("/content/danaher/ls", "")
-
-    if (anchors[i].href.includes("?") || anchors[i].href.includes("lifesciences.danaher.com") ) {
-
-    } else {
-        anchors[i].href = anchors[i].href.concat("?utm_source=dhls_website")
-    }
-}
-
-}
-</component >
-
-<component :is="'style'">
-    .btn.orange {
-        background-color: #dc6016;
-        color: white;
-    }
-</component ></div>
 </div>
 
         
@@ -1412,7 +1283,7 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
 
     
     
-<script src="/etc.clientlibs/core/wcm/components/commons/datalayer/v1/clientlibs/core.wcm.components.commons.datalayer.v1.lc-904d3c2f1e821ab45124d66de422b409-lc.min.js"></script>
+<script src="/etc.clientlibs/core/wcm/components/commons/datalayer/v1/clientlibs/core.wcm.components.commons.datalayer.v1.lc-70264651675213ed7f7cc5a02a00f621-lc.min.js"></script>
 
 
 
@@ -1422,14 +1293,14 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
         
     
 <script src="/etc.clientlibs/core/wcm/components/commons/site/clientlibs/container.lc-0a6aff292f5cc42142779cde92054524-lc.min.js"></script>
-<script src="/etc.clientlibs/danaher/clientlibs/clientlib-base.lc-d2ce98f15d18ed03c818947635149abb-lc.min.js"></script>
+<script src="/etc.clientlibs/danaher/clientlibs/clientlib-base.lc-2a85512656f79a4d72626fea0d606318-lc.min.js"></script>
 
 
 
 
     
 <script src="/etc.clientlibs/danaher/clientlibs/clientlib-dependencies.lc-d41d8cd98f00b204e9800998ecf8427e-lc.min.js"></script>
-<script src="/etc.clientlibs/danaher/clientlibs/clientlib-site.lc-7ba46db2b072016ab9ddfd178cec52ba-lc.min.js"></script>
+<script src="/etc.clientlibs/danaher/clientlibs/clientlib-site.lc-26d30872729a07b9af9948e2214046af-lc.min.js"></script>
 
 
 
@@ -1500,6 +1371,8 @@ <h3 class="text-sm font-semibold text-white tracking-wider uppercase">Subscribe
 
 </script>
 
+<script src="https://cdn.usefathom.com/script.js" data-site="KGTBOGMR" defer></script>
+
 
     
 </body>
diff --git a/tools/importer/transformers/util.js b/tools/importer/transformers/util.js
index bf1b3b591..2f0dee169 100644
--- a/tools/importer/transformers/util.js
+++ b/tools/importer/transformers/util.js
@@ -189,18 +189,75 @@ export const pdfembed = (embedEl, document) => {
   embedEl.append(table);
 };
 
+const getVideoThumbnail = (url, quality) => {
+  if (url) {
+    let videoId;
+    let thumbnail;
+    let type;
+    if (url.match(/youtube\.com.*(\?v=|\/embed\/)(.{11})/) || url.match(/youtu.be\/(.{11})/)) {
+      const result = url.match(/youtube\.com.*(\?v=|\/embed\/)(.{11})/);
+      videoId = result.pop();
+      type = 'youtube';
+    } else if (url.match(/vimeo.*\/(\d+)/i)) {
+      videoId = url.match(/vimeo.*\/(\d+)/i);
+      type = 'vimeo';
+    } else if (url.split('/').pop() !== 'watch') {
+      videoId = url.split('/').pop();
+      type = 'vidyard';
+    }
+    if (videoId) {
+      if (typeof quality !== 'undefined') {
+        let qualityKey = 'maxresdefault'; // Max quality
+        if (quality === 'low') {
+          qualityKey = 'sddefault';
+        } else if (quality === 'medium') {
+          qualityKey = 'mqdefault';
+        } else if (quality === 'high') {
+          qualityKey = 'hqdefault';
+        }
+        if (type === 'youtube') {
+          thumbnail = `http://img.youtube.com/vi/${videoId}/${qualityKey}.jpg`;
+        } else if (type === 'vimeo') {
+          thumbnail = `https://vimeo.com/api/oembed.json?url=https%3A//vimeo.com/${videoId}`;
+        } else if (type === 'vidyard') {
+          thumbnail = `http://share.vidyard.com/watch/${videoId}`;
+        } else {
+          thumbnail = false;
+        }
+      }
+      return thumbnail;
+    }
+  }
+  return false;
+};
+
 export const videoembed = (embedEl, document) => {
   const videoEl = embedEl?.querySelector('iframe');
-  embedEl.innerHTML = '';
   const anc = document.createElement('a');
   let href = videoEl.getAttribute('src');
   if (!href.startsWith('https:') && href.includes('vidyard')) {
     if (href[href.length - 1] === '?') href = href.slice(0, -1);
     href = `https:${href}`;
   }
+  const div = document.createElement('div');
+  const p1 = document.createElement('p');
+  const thumbnail = getVideoThumbnail(href, 'max');
+  if (thumbnail) {
+    const img = document.createElement('img');
+    img.src = thumbnail;
+    p1.append(img);
+    div.append(p1);
+  }
   anc.href = href;
-  anc.textContent = 'Video Player';
-  embedEl.append(anc);
+  const p2 = document.createElement('p');
+  if (href) {
+    p2.append([anc]);
+    div.append(p2);
+  }
+  const cells = [['Video Player'], [div]];
+  const block = WebImporter.DOMUtils.createTable(cells, document);
+  embedEl.innerHTML = '';
+  embedEl.append(block);
   return embedEl;
 };