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		<title><![CDATA[Cellagen Technology: Featured Products]]></title>
		<link>https://www.cellagentech.com</link>
		<description><![CDATA[A list of the featured products at Cellagen Technology.]]></description>
		<pubDate>Sun, 10 May 2026 11:55:26 +0000</pubDate>
		<isc:store_title><![CDATA[Cellagen Technology]]></isc:store_title>
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			<title><![CDATA[FlexiWash FW400]]></title>
			<link>https://www.cellagentech.com/flexiwash-fw400/</link>
			<pubDate>Wed, 07 Jun 2017 12:37:01 +0000</pubDate>
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			<description><![CDATA[<div style='float: right; padding: 10px;'><a href="https://www.cellagentech.com/flexiwash-fw400/"><img src="https://cdn11.bigcommerce.com/s-72skw3/products/313/images/696/FW400-front__42350.1496864300.120.120.png?c=2" alt="FW400 Front View" /></a></div><div id="Introduction" class="wrap">
<div class="head"><span style="font-size: large;">INTRODUCTION</span></div>
<p>The FlexiWash FW400 Automatic Membrane/Gel Wash Station is designed for automated Western blot membrane wash and incubation process. After proteins are transferred onto a membrane,..<p> </p>]]></description>
			<content:encoded><![CDATA[<div style='float: right; padding: 10px;'><a href="https://www.cellagentech.com/flexiwash-fw400/"><img src="https://cdn11.bigcommerce.com/s-72skw3/products/313/images/696/FW400-front__42350.1496864300.120.120.png?c=2" alt="FW400 Front View" /></a></div><div id="Introduction" class="wrap">
<div class="head"><span style="font-size: large;">INTRODUCTION</span></div>
<p>The FlexiWash FW400 Automatic Membrane/Gel Wash Station is designed for automated Western blot membrane wash and incubation process. After proteins are transferred onto a membrane,..<p> </p>]]></content:encoded>
			<isc:description><![CDATA[<div id="Introduction" class="wrap">
<div class="head"><span style="font-size: large;">INTRODUCTION</span></div>
<p>The FlexiWash FW400 Automatic Membrane/Gel Wash Station is designed for automated Western blot membrane wash and incubation process. After proteins are transferred onto a membrane,..]]></isc:description>
			<isc:productid><![CDATA[313]]></isc:productid>
			<isc:thumb><![CDATA[https://cdn11.bigcommerce.com/s-72skw3/products/313/images/696/FW400-front__42350.1496864300.120.120.png?c=2]]></isc:thumb>
			<isc:image><![CDATA[https://cdn11.bigcommerce.com/s-72skw3/products/313/images/696/FW400-front__42350.1496864300.1280.1280.png?c=2]]></isc:image>
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		<item>
			<title><![CDATA[TMP195 | Class IIa HDAC inhibitor]]></title>
			<link>https://www.cellagentech.com/tmp195/</link>
			<pubDate>Tue, 23 Jul 2013 11:52:20 +0000</pubDate>
			<guid isPermaLink="false">https://www.cellagentech.com/tmp195/</guid>
			<description><![CDATA[<div style='float: right; padding: 10px;'><a href="https://www.cellagentech.com/tmp195/"><img src="https://cdn11.bigcommerce.com/s-72skw3/products/288/images/643/TMP195__94693.1771532497.120.120.png?c=2" alt="TMP195, 400x400px, png" /></a></div><p>TMP195 is the most potent and selective class IIa HDAC inhibitor identified to date, with IC50s of 59 nM, 60 nM, 26 nM and 15 nM for HDAC4, HDAC5, HDAC7 and HDAC9 respectively. It has over 100-fold selectivity targeting other HDACs (IC50s&gt;10 &micro;M). TMP195 has an unprecedented zinc-bindin..<p><strong>Price: $159.00</strong> </p>]]></description>
			<content:encoded><![CDATA[<div style='float: right; padding: 10px;'><a href="https://www.cellagentech.com/tmp195/"><img src="https://cdn11.bigcommerce.com/s-72skw3/products/288/images/643/TMP195__94693.1771532497.120.120.png?c=2" alt="TMP195, 400x400px, png" /></a></div><p>TMP195 is the most potent and selective class IIa HDAC inhibitor identified to date, with IC50s of 59 nM, 60 nM, 26 nM and 15 nM for HDAC4, HDAC5, HDAC7 and HDAC9 respectively. It has over 100-fold selectivity targeting other HDACs (IC50s&gt;10 &micro;M). TMP195 has an unprecedented zinc-bindin..<p><strong>Price: $159.00</strong> </p>]]></content:encoded>
			<isc:description><![CDATA[<p>TMP195 is the most potent and selective class IIa HDAC inhibitor identified to date, with IC50s of 59 nM, 60 nM, 26 nM and 15 nM for HDAC4, HDAC5, HDAC7 and HDAC9 respectively. It has over 100-fold selectivity targeting other HDACs (IC50s&gt;10 &micro;M). TMP195 has an unprecedented zinc-bindin..]]></isc:description>
			<isc:productid><![CDATA[288]]></isc:productid>
			<isc:thumb><![CDATA[https://cdn11.bigcommerce.com/s-72skw3/products/288/images/643/TMP195__94693.1771532497.120.120.png?c=2]]></isc:thumb>
			<isc:image><![CDATA[https://cdn11.bigcommerce.com/s-72skw3/products/288/images/643/TMP195__94693.1771532497.1280.1280.png?c=2]]></isc:image>
			<isc:price><![CDATA[$159.00]]></isc:price>
		</item>
		<item>
			<title><![CDATA[TMP269 | Class IIa HDAC inhibitor]]></title>
			<link>https://www.cellagentech.com/tmp269/</link>
			<pubDate>Tue, 23 Jul 2013 11:33:01 +0000</pubDate>
			<guid isPermaLink="false">https://www.cellagentech.com/tmp269/</guid>
			<description><![CDATA[<div style='float: right; padding: 10px;'><a href="https://www.cellagentech.com/tmp269/"><img src="https://cdn11.bigcommerce.com/s-72skw3/products/287/images/639/TMP269__23972.1771532503.120.120.png?c=2" alt="TMP269, 400x400px, png" /></a></div><p>TMP269 is a highly potent and selective class IIa HDAC inhibitor identified, with IC50s of 126 nM, 80 nM, 36 nM and 19 nM for HDAC4, HDAC5, HDAC7 and HDAC9 respectively. TMP269 has an unprecedented metal-binding group, trifluoromethyloxadiazole (TFMO). The co-crystal structure of TMP 269 and HD..<p><strong>Price: $139.00</strong> </p>]]></description>
			<content:encoded><![CDATA[<div style='float: right; padding: 10px;'><a href="https://www.cellagentech.com/tmp269/"><img src="https://cdn11.bigcommerce.com/s-72skw3/products/287/images/639/TMP269__23972.1771532503.120.120.png?c=2" alt="TMP269, 400x400px, png" /></a></div><p>TMP269 is a highly potent and selective class IIa HDAC inhibitor identified, with IC50s of 126 nM, 80 nM, 36 nM and 19 nM for HDAC4, HDAC5, HDAC7 and HDAC9 respectively. TMP269 has an unprecedented metal-binding group, trifluoromethyloxadiazole (TFMO). The co-crystal structure of TMP 269 and HD..<p><strong>Price: $139.00</strong> </p>]]></content:encoded>
			<isc:description><![CDATA[<p>TMP269 is a highly potent and selective class IIa HDAC inhibitor identified, with IC50s of 126 nM, 80 nM, 36 nM and 19 nM for HDAC4, HDAC5, HDAC7 and HDAC9 respectively. TMP269 has an unprecedented metal-binding group, trifluoromethyloxadiazole (TFMO). The co-crystal structure of TMP 269 and HD..]]></isc:description>
			<isc:productid><![CDATA[287]]></isc:productid>
			<isc:thumb><![CDATA[https://cdn11.bigcommerce.com/s-72skw3/products/287/images/639/TMP269__23972.1771532503.120.120.png?c=2]]></isc:thumb>
			<isc:image><![CDATA[https://cdn11.bigcommerce.com/s-72skw3/products/287/images/639/TMP269__23972.1771532503.1280.1280.png?c=2]]></isc:image>
			<isc:price><![CDATA[$139.00]]></isc:price>
		</item>
		<item>
			<title><![CDATA[GSK126 | EZH2 inhibitor]]></title>
			<link>https://www.cellagentech.com/gsk126/</link>
			<pubDate>Thu, 16 May 2013 03:11:22 +0000</pubDate>
			<guid isPermaLink="false">https://www.cellagentech.com/gsk126/</guid>
			<description><![CDATA[<div style='float: right; padding: 10px;'><a href="https://www.cellagentech.com/gsk126/"><img src="https://cdn11.bigcommerce.com/s-72skw3/products/242/images/552/GSK126__24471.1771531213.120.120.png?c=2" alt="GSK126, 400x400px, png" /></a></div><p>GSK126 is an indole-based inhibitor of EZH2 methyltransferase activity, with an Ki-app of 0.5-3 nM independent of substrate used. It is competitive with S-adenosyl methionine (SAM) and non-competitive with peptide substrates. GSK126 is highly selective against many other protein classes and met..<p><strong>Price: $159.00</strong> </p>]]></description>
			<content:encoded><![CDATA[<div style='float: right; padding: 10px;'><a href="https://www.cellagentech.com/gsk126/"><img src="https://cdn11.bigcommerce.com/s-72skw3/products/242/images/552/GSK126__24471.1771531213.120.120.png?c=2" alt="GSK126, 400x400px, png" /></a></div><p>GSK126 is an indole-based inhibitor of EZH2 methyltransferase activity, with an Ki-app of 0.5-3 nM independent of substrate used. It is competitive with S-adenosyl methionine (SAM) and non-competitive with peptide substrates. GSK126 is highly selective against many other protein classes and met..<p><strong>Price: $159.00</strong> </p>]]></content:encoded>
			<isc:description><![CDATA[<p>GSK126 is an indole-based inhibitor of EZH2 methyltransferase activity, with an Ki-app of 0.5-3 nM independent of substrate used. It is competitive with S-adenosyl methionine (SAM) and non-competitive with peptide substrates. GSK126 is highly selective against many other protein classes and met..]]></isc:description>
			<isc:productid><![CDATA[242]]></isc:productid>
			<isc:thumb><![CDATA[https://cdn11.bigcommerce.com/s-72skw3/products/242/images/552/GSK126__24471.1771531213.120.120.png?c=2]]></isc:thumb>
			<isc:image><![CDATA[https://cdn11.bigcommerce.com/s-72skw3/products/242/images/552/GSK126__24471.1771531213.1280.1280.png?c=2]]></isc:image>
			<isc:price><![CDATA[$159.00]]></isc:price>
		</item>
		<item>
			<title><![CDATA[SU5402 | FGFR/VEGFR/PDGFR inhibitor]]></title>
			<link>https://www.cellagentech.com/su5402/</link>
			<pubDate>Wed, 13 Mar 2013 12:15:23 +0000</pubDate>
			<guid isPermaLink="false">https://www.cellagentech.com/su5402/</guid>
			<description><![CDATA[<div style='float: right; padding: 10px;'><a href="https://www.cellagentech.com/su5402/"><img src="https://cdn11.bigcommerce.com/s-72skw3/products/216/images/273/SU5402__05530.1771532329.120.120.png?c=2" alt="SU5402, 400x400px, png" /></a></div><p>SU5402 is a fibroblast growth factor receptor (FGFR)-specific tyrosine kinase inhibitor with IC50 ~0.03&micro;M. Multiple myeloma studies suggest that SU 5402 inhibits FGFR3 phosphorylation in vitro.&nbsp;SU5402 is also very potent in inhibiting VEGFR, and PDGFR.&nbsp; Research shows that it in..<p><strong>Price: <span class="SalePrice">$59.00</span></strong> </p>]]></description>
			<content:encoded><![CDATA[<div style='float: right; padding: 10px;'><a href="https://www.cellagentech.com/su5402/"><img src="https://cdn11.bigcommerce.com/s-72skw3/products/216/images/273/SU5402__05530.1771532329.120.120.png?c=2" alt="SU5402, 400x400px, png" /></a></div><p>SU5402 is a fibroblast growth factor receptor (FGFR)-specific tyrosine kinase inhibitor with IC50 ~0.03&micro;M. Multiple myeloma studies suggest that SU 5402 inhibits FGFR3 phosphorylation in vitro.&nbsp;SU5402 is also very potent in inhibiting VEGFR, and PDGFR.&nbsp; Research shows that it in..<p><strong>Price: <span class="SalePrice">$59.00</span></strong> </p>]]></content:encoded>
			<isc:description><![CDATA[<p>SU5402 is a fibroblast growth factor receptor (FGFR)-specific tyrosine kinase inhibitor with IC50 ~0.03&micro;M. Multiple myeloma studies suggest that SU 5402 inhibits FGFR3 phosphorylation in vitro.&nbsp;SU5402 is also very potent in inhibiting VEGFR, and PDGFR.&nbsp; Research shows that it in..]]></isc:description>
			<isc:productid><![CDATA[216]]></isc:productid>
			<isc:thumb><![CDATA[https://cdn11.bigcommerce.com/s-72skw3/products/216/images/273/SU5402__05530.1771532329.120.120.png?c=2]]></isc:thumb>
			<isc:image><![CDATA[https://cdn11.bigcommerce.com/s-72skw3/products/216/images/273/SU5402__05530.1771532329.1280.1280.png?c=2]]></isc:image>
			<isc:price><![CDATA[<span class="SalePrice">$59.00</span>]]></isc:price>
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