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	<title>Nascent Protein Synthesis &#8211; VectorLabs</title>
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	<title>Nascent Protein Synthesis &#8211; VectorLabs</title>
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		<title>O-propargyl-puromycine (OPP)</title>
		<link>https://staging.vectorlabs.com/products/o-propargyl-puromycine-opp/</link>
		
		<dc:creator><![CDATA[Vector Laboratories R&D]]></dc:creator>
		<pubDate>Tue, 19 Sep 2023 19:32:43 +0000</pubDate>
				<guid isPermaLink="false">https://staging.vectorlabs.com/?post_type=product&#038;p=22065</guid>

					<description><![CDATA[<h3>Description</h3>
<p>O-propargyl-puromycin (OPP) is an alkyne analog of puromycin that is efficiently incorporated into newly translated proteins, which are rapidly turned over by the proteasome and can be visualized or captured by copper(I)-catalyzed azide-alkyne cycloaddition. Unlike methionine analogs, OPP does not require methionine-free conditions and, uniquely, can be used to label and assay nascent proteins in whole organisms.</p>
<h3>Specifications</h3>
<table id="product-attribute-specs-table" class="data table additional-attributes" width="585">
<tbody>
<tr>
<th class="col label" scope="row">Unit Size</th>
<td class="col data" data-th="Unit Size">5 mg, 25 mg, 100 mg</td>
</tr>
<tr>
<th class="col label" scope="row">Molecular weight</th>
<td class="col data" data-th="Applications">495.54</td>
</tr>
<tr>
<th class="col label" scope="row">Chemical composition</th>
<td class="col data" data-th="Target Species">C24H29N7O5</td>
</tr>
<tr>
<th class="col label" scope="row">CAS</th>
<td class="col data" data-th="Conjugate">1416561-90-4</td>
</tr>
<tr>
<th class="col label" scope="row">Solubility</th>
<td class="col data" data-th="Format">DMSO, DMF</td>
</tr>
<tr>
<th class="col label" scope="row">Purity</th>
<td class="col data" data-th="Format">&#62;95% (HPLC)</td>
</tr>
<tr>
<th class="col label" scope="row">Appearance</th>
<td class="col data" data-th="Format">Off-white to slightly grey crystalline</td>
</tr>
<tr>
<th class="col label" scope="row">Storage Conditions</th>
<td class="col data" data-th="Format">-20°C.</td>
</tr>
<tr>
<th class="col label" scope="row">Shipping Conditions</th>
<td class="col data" data-th="Format">Ambient temperature</td>
</tr>
</tbody>
</table>
<p>The post <a rel="nofollow" href="https://staging.vectorlabs.com/products/o-propargyl-puromycine-opp/">O-propargyl-puromycine (OPP)</a> appeared first on <a rel="nofollow" href="https://staging.vectorlabs.com">VectorLabs</a>.</p>
]]></description>
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                                                            <h2 class="eael-tab-title title-after-icon" >Description</h2>                                                    </li>
                                            <li id="specifications" class="inactive eael-tab-item-trigger eael-tab-nav-item" aria-selected="false" data-tab="2" role="tab" tabindex="-1" aria-controls="specifications-tab" aria-expanded="false">
                            
                            
                            
                                                            <h2 class="eael-tab-title title-after-icon" >Specifications</h2>                                                    </li>
                                            <li id="documents" class="inactive eael-tab-item-trigger eael-tab-nav-item" aria-selected="false" data-tab="3" role="tab" tabindex="-1" aria-controls="documents-tab" aria-expanded="false">
                            
                            
                            
                                                            <h2 class="eael-tab-title title-after-icon" >Documents</h2>                                                    </li>
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                                                            <h2 class="eael-tab-title title-after-icon" >Selected References</h2>                                                    </li>
                                    </ul>
            </div>
            
            <div class="eael-tabs-content">
		        
                    <div id="description-tab" class="clearfix eael-tab-content-item inactive" data-title-link="description-tab">
				        <h3>Description</h3><p>O-propargyl-puromycin (OPP) is an alkyne analog of puromycin that is efficiently incorporated into newly translated proteins, which are rapidly turned over by the proteasome and can be visualized or captured by copper(I)-catalyzed azide-alkyne cycloaddition. Unlike methionine analogs, OPP does not require methionine-free conditions and, uniquely, can be used to label and assay nascent proteins in whole organisms.</p>                    </div>
		        
                    <div id="specifications-tab" class="clearfix eael-tab-content-item inactive" data-title-link="specifications-tab">
				        <h3>Specifications</h3><table id="product-attribute-specs-table" class="data table additional-attributes" style="height: 186px;" width="585"><tbody><tr><th class="col label" scope="row">Unit Size</th><td class="col data" data-th="Unit Size">5 mg, 25 mg, 100 mg</td></tr><tr><th class="col label" scope="row">Molecular weight</th><td class="col data" data-th="Applications">495.54</td></tr><tr><th class="col label" scope="row">Chemical composition</th><td class="col data" data-th="Target Species">C24H29N7O5</td></tr><tr><th class="col label" scope="row">CAS</th><td class="col data" data-th="Conjugate">1416561-90-4</td></tr><tr><th class="col label" scope="row">Solubility</th><td class="col data" data-th="Format">DMSO, DMF</td></tr><tr><th class="col label" scope="row">Purity</th><td class="col data" data-th="Format">&gt;95% (HPLC)</td></tr><tr><th class="col label" scope="row">Appearance</th><td class="col data" data-th="Format">Off-white to slightly grey crystalline</td></tr><tr><th class="col label" scope="row">Storage Conditions</th><td class="col data" data-th="Format">-20°C.</td></tr><tr><th class="col label" scope="row">Shipping Conditions</th><td class="col data" data-th="Format">Ambient temperature</td></tr></tbody></table>                    </div>
		        
                    <div id="documents-tab" class="clearfix eael-tab-content-item inactive" data-title-link="documents-tab">
				        <h3>Documents</h3><div class="explorer_section applications container documentSection catalog-product-document"><ul class="document_list"><li class="documentContainer documentItem"><a class="documentTitle" href="https://staging.vectorlabs.com/productattachments/sds/VL_CCT-1407_sds.pdf">Safety Data Sheet</a></li><li><a href="https://staging.vectorlabs.com/resources/certificate-of-analysis/">Download CoA</a></li><li><a class="woocommerce-print-products-pdf-link" href="https://staging.vectorlabs.com/products/o-propargyl-puromycine-opp/?print-products=pdf" target="_blank">Datasheet</a></li></ul></div>                    </div>
		        
                    <div id="selected-references-tab" class="clearfix eael-tab-content-item inactive" data-title-link="selected-references-tab">
				        <h3>Selected References</h3><ol><li>Leach, R. W., <em>et al.</em> (2021). Activity-based RNA-modifying enzyme probing reveals DUS3L-mediated dihydrouridylation. <em>Nat Chem Biol.</em>, <strong>17 (11)</strong>, 1178-1187. [<a href="https://pubmed.ncbi.nlm.nih.gov/34556860/" target="_blank" rel="noopener">PubMed</a>]</li><li>Morral, C., <em>et al.</em> (2020). Zonation of Ribosomal DNA Transcription Defines a Stem Cell Hierarchy in Colorectal Cancer. <em>Cell Stem Cell.</em>, <strong>26 (6)</strong>, 845-861.e12. [<a href="https://pubmed.ncbi.nlm.nih.gov/32396863/" target="_blank" rel="noopener">PubMed</a>]</li><li>Uchiyama, J., <em>et al.</em> (2020). Quantitative nascent proteome profiling by dual pulse labeling with O-propargyl-puromycin and stable isotope labeled amino acids. <em>The Journal of Biochemistry</em>, <strong>10</strong>, 1093. [<a href="https://academic.oup.com/jb/advance-article/doi/10.1093/jb/mvaa104/5905495" target="_blank" rel="noopener">Oxford Academic</a>]</li><li>Lui, J., <em>et al.</em> (2012). Imaging protein synthesis in cells and tissues with an alkyne analog of puromycin. <em>PNAS</em>, <strong>109</strong>, 413-8. [<a href="https://www.ncbi.nlm.nih.gov/pubmed/22160674" target="_blank" rel="noopener">PubMed</a>]</li><li>Forester, C.M., <em>et al</em>. (2018). Revealing nascent proteomics in signaling pathways and cell differentiation.<em>PNAS</em>, <strong>115</strong>, 2353-8. [<a href="https://www.ncbi.nlm.nih.gov/pubmed/29467287" target="_blank" rel="noopener">PubMed</a>]</li><li>Tong, M., <em>et al</em>. (2020). Effective Method for Accurate and Sensitive Quantitation of Rapid Changes of Newly Synthesized Proteins. <em>Anal. Chem.</em>, <strong>92(14)</strong>, 10048-57. [<a href="https://pubmed.ncbi.nlm.nih.gov/32531160/" target="_blank" rel="noopener">PubMed</a>]</li></ol>                    </div>
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		<p>The post <a rel="nofollow" href="https://staging.vectorlabs.com/products/o-propargyl-puromycine-opp/">O-propargyl-puromycine (OPP)</a> appeared first on <a rel="nofollow" href="https://staging.vectorlabs.com">VectorLabs</a>.</p>
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		<item>
		<title>4-Azido-L-phenylalanine</title>
		<link>https://staging.vectorlabs.com/products/4-azido-l-phenylalanine/</link>
		
		<dc:creator><![CDATA[Vector Laboratories R&D]]></dc:creator>
		<pubDate>Tue, 19 Sep 2023 19:23:37 +0000</pubDate>
				<guid isPermaLink="false">https://staging.vectorlabs.com/?post_type=product&#038;p=21867</guid>

					<description><![CDATA[<h3>Description</h3>
<p>4-Azido-L-phenylalanine is an unnatural derivative of L-phenylalanine that can be incorporated by recombinant methods into proteins allowing site-specific modification, e.g. by ‘click chemistry’, Staudinger reaction, or by UV-irradiation at 254 nm. The azido-modified protein can be detected with either fluorescent alkyne or biotin alkyne. Detection sensitivity with these reagents in 1-D gels and Western blots is in the low femtomole range and compatible with downstream LC-MS⁄MS and MALDI MS analysis.</p>
<h3>Specifications</h3>
<table id="product-attribute-specs-table" class="data table additional-attributes" width="585">
<tbody>
<tr>
<th class="col label" scope="row">Unit Size</th>
<td class="col data" data-th="Unit Size">1 g, 5 g, 25 g</td>
</tr>
<tr>
<th class="col label" scope="row">Molecular weight</th>
<td class="col data" data-th="Applications"><span data-olk-copy-source="MessageBody">242.66</span></td>
</tr>
<tr>
<th class="col label" scope="row">Chemical composition</th>
<td class="col data" data-th="Target Species">C9H10N4O2</td>
</tr>
<tr>
<th class="col label" scope="row">CAS</th>
<td class="col data" data-th="Conjugate">33173-53-4</td>
</tr>
<tr>
<th class="col label" scope="row">Solubility</th>
<td class="col data" data-th="Format">Water, DMSO, DMF</td>
</tr>
<tr>
<th class="col label" scope="row">Purity</th>
<td class="col data" data-th="Format">&#62;95% (H NMR)</td>
</tr>
<tr>
<th class="col label" scope="row">Appearance</th>
<td class="col data" data-th="Format">Off-white to slightly grey crystalline</td>
</tr>
<tr>
<th class="col label" scope="row">Storage Conditions</th>
<td class="col data" data-th="Format">-20°C.</td>
</tr>
<tr>
<th class="col label" scope="row">Shipping Conditions</th>
<td class="col data" data-th="Format">Ambient temperature</td>
</tr>
</tbody>
</table>
<p>The post <a rel="nofollow" href="https://staging.vectorlabs.com/products/4-azido-l-phenylalanine/">4-Azido-L-phenylalanine</a> appeared first on <a rel="nofollow" href="https://staging.vectorlabs.com">VectorLabs</a>.</p>
]]></description>
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                                                            <h2 class="eael-tab-title title-after-icon" >Description</h2>                                                    </li>
                                            <li id="specifications" class="inactive eael-tab-item-trigger eael-tab-nav-item" aria-selected="false" data-tab="2" role="tab" tabindex="-1" aria-controls="specifications-tab" aria-expanded="false">
                            
                            
                            
                                                            <h2 class="eael-tab-title title-after-icon" >Specifications</h2>                                                    </li>
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                    <div id="description-tab" class="clearfix eael-tab-content-item inactive" data-title-link="description-tab">
				        <h3>Description</h3><p>4-Azido-L-phenylalanine is an unnatural derivative of L-phenylalanine that can be incorporated by recombinant methods into proteins allowing site-specific modification, e.g. by ‘click chemistry’, Staudinger reaction, or by UV-irradiation at 254 nm. The azido-modified protein can be detected with either fluorescent alkyne or biotin alkyne. Detection sensitivity with these reagents in 1-D gels and Western blots is in the low femtomole range and compatible with downstream LC-MS⁄MS and MALDI MS analysis.</p>                    </div>
		        
                    <div id="specifications-tab" class="clearfix eael-tab-content-item inactive" data-title-link="specifications-tab">
				        <h3>Specifications</h3><table id="product-attribute-specs-table" class="data table additional-attributes" style="height: 186px;" width="585"><tbody><tr><th class="col label" scope="row">Unit Size</th><td class="col data" data-th="Unit Size">1 g, 5 g, 25 g</td></tr><tr><th class="col label" scope="row">Molecular weight</th><td class="col data" data-th="Applications">242.66</td></tr><tr><th class="col label" scope="row">Chemical composition</th><td class="col data" data-th="Target Species">C9H10N4O2</td></tr><tr><th class="col label" scope="row">CAS</th><td class="col data" data-th="Conjugate">33173-53-4</td></tr><tr><th class="col label" scope="row">Solubility</th><td class="col data" data-th="Format">Water, DMSO, DMF</td></tr><tr><th class="col label" scope="row">Purity</th><td class="col data" data-th="Format">&gt;95% (H NMR)</td></tr><tr><th class="col label" scope="row">Appearance</th><td class="col data" data-th="Format">Off-white to slightly grey crystalline</td></tr><tr><th class="col label" scope="row">Storage Conditions</th><td class="col data" data-th="Format">-20°C.</td></tr><tr><th class="col label" scope="row">Shipping Conditions</th><td class="col data" data-th="Format">Ambient temperature</td></tr></tbody></table>                    </div>
		        
                    <div id="documents-tab" class="clearfix eael-tab-content-item inactive" data-title-link="documents-tab">
				        <h3>Documents</h3><div class="explorer_section applications container documentSection catalog-product-document"><ul class="document_list"><li class="documentContainer documentItem"><a class="documentTitle" href="https://staging.vectorlabs.com/productattachments/sds/VL_CCT-1406_sds.pdf">Safety Data Sheet</a></li><li><a href="https://staging.vectorlabs.com/resources/certificate-of-analysis/">Download CoA</a></li><li><a class="woocommerce-print-products-pdf-link" href="https://staging.vectorlabs.com/products/4-azido-l-phenylalanine/?print-products=pdf" target="_blank">Datasheet</a></li></ul></div>                    </div>
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		<p>The post <a rel="nofollow" href="https://staging.vectorlabs.com/products/4-azido-l-phenylalanine/">4-Azido-L-phenylalanine</a> appeared first on <a rel="nofollow" href="https://staging.vectorlabs.com">VectorLabs</a>.</p>
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			</item>
		<item>
		<title>L-Homopropargylglycine (HPG)</title>
		<link>https://staging.vectorlabs.com/products/l-homopropargylglycine-hpg/</link>
		
		<dc:creator><![CDATA[Vector Laboratories R&D]]></dc:creator>
		<pubDate>Tue, 19 Sep 2023 19:15:27 +0000</pubDate>
				<guid isPermaLink="false">https://staging.vectorlabs.com/?post_type=product&#038;p=21753</guid>

					<description><![CDATA[<h3>Description</h3>
<p>L-Homopropargylglycine (HPG) is an amino acid analog of methionine that contains a very small modification, specifically an alkyne moiety that can be fed to cultured cells and incorporated into proteins during active protein synthesis. Detection utilizes the chemoselective ligation or “click ” reaction between an azide and an alkyne or cyclooctyne. The alkyne-modified protein is detected with either fluorescent azide or biotin azide. Detection sensitivity with these reagents in 1-D gels and Western blots is in the low femtomole range and compatible with downstream LC-MS⁄MS and MALDI MS analysis.</p>
<h3>Specifications</h3>
<table id="product-attribute-specs-table" class="data table additional-attributes" width="585">
<tbody>
<tr>
<th class="col label" scope="row">Unit Size</th>
<td class="col data" data-th="Unit Size">25 mg, 100 mg, 1000 mg</td>
</tr>
<tr>
<th class="col label" scope="row">Molecular weight</th>
<td class="col data" data-th="Applications">163.60 (HCl salt)</td>
</tr>
<tr>
<th class="col label" scope="row">Chemical composition</th>
<td class="col data" data-th="Target Species">C6H10ClNO2</td>
</tr>
<tr>
<th class="col label" scope="row">CAS</th>
<td class="col data" data-th="Conjugate">942518-19-6</td>
</tr>
<tr>
<th class="col label" scope="row">Solubility</th>
<td class="col data" data-th="Format">Water, DMSO, DMF</td>
</tr>
<tr>
<th class="col label" scope="row">Purity</th>
<td class="col data" data-th="Format">&#62;95% (H NMR)</td>
</tr>
<tr>
<th class="col label" scope="row">Appearance</th>
<td class="col data" data-th="Format">White crystalline</td>
</tr>
<tr>
<th class="col label" scope="row">Storage Conditions</th>
<td class="col data" data-th="Format">-20°C.</td>
</tr>
<tr>
<th class="col label" scope="row">Shipping Conditions</th>
<td class="col data" data-th="Format">Ambient temperature</td>
</tr>
</tbody>
</table>
<p>The post <a rel="nofollow" href="https://staging.vectorlabs.com/products/l-homopropargylglycine-hpg/">L-Homopropargylglycine (HPG)</a> appeared first on <a rel="nofollow" href="https://staging.vectorlabs.com">VectorLabs</a>.</p>
]]></description>
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                                                            <h2 class="eael-tab-title title-after-icon" >Description</h2>                                                    </li>
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                                                            <h2 class="eael-tab-title title-after-icon" >Specifications</h2>                                                    </li>
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                                                            <h2 class="eael-tab-title title-after-icon" >Selected References</h2>                                                    </li>
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				        <h3>Description</h3><p>L-Homopropargylglycine (HPG) is an amino acid analog of methionine that contains a very small modification, specifically an alkyne moiety that can be fed to cultured cells and incorporated into proteins during active protein synthesis. Detection utilizes the chemoselective ligation or “click ” reaction between an azide and an alkyne or cyclooctyne. The alkyne-modified protein is detected with either fluorescent azide or biotin azide. Detection sensitivity with these reagents in 1-D gels and Western blots is in the low femtomole range and compatible with downstream LC-MS⁄MS and MALDI MS analysis.</p>                    </div>
		        
                    <div id="specifications-tab" class="clearfix eael-tab-content-item inactive" data-title-link="specifications-tab">
				        <h3>Specifications</h3><table id="product-attribute-specs-table" class="data table additional-attributes" style="height: 186px;" width="585"><tbody><tr><th class="col label" scope="row">Unit Size</th><td class="col data" data-th="Unit Size">25 mg, 100 mg, 1000 mg</td></tr><tr><th class="col label" scope="row">Molecular weight</th><td class="col data" data-th="Applications">163.60 (HCl salt)</td></tr><tr><th class="col label" scope="row">Chemical composition</th><td class="col data" data-th="Target Species">C6H10ClNO2</td></tr><tr><th class="col label" scope="row">CAS</th><td class="col data" data-th="Conjugate">942518-19-6</td></tr><tr><th class="col label" scope="row">Solubility</th><td class="col data" data-th="Format">Water, DMSO, DMF</td></tr><tr><th class="col label" scope="row">Purity</th><td class="col data" data-th="Format">&gt;95% (H NMR)</td></tr><tr><th class="col label" scope="row">Appearance</th><td class="col data" data-th="Format">White crystalline</td></tr><tr><th class="col label" scope="row">Storage Conditions</th><td class="col data" data-th="Format">-20°C.</td></tr><tr><th class="col label" scope="row">Shipping Conditions</th><td class="col data" data-th="Format">Ambient temperature</td></tr></tbody></table>                    </div>
		        
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				        <h3>Documents</h3><div class="explorer_section applications container documentSection catalog-product-document"><ul class="document_list"><li class="documentContainer documentItem"><a class="documentTitle" href="https://staging.vectorlabs.com/productattachments/sds/VL_CCT-1067_sds.pdf">Safety Data Sheet</a></li><li><a href="https://staging.vectorlabs.com/resources/certificate-of-analysis/">Download CoA</a></li><li><a class="woocommerce-print-products-pdf-link" href="https://staging.vectorlabs.com/products/l-homopropargylglycine-hpg/?print-products=pdf" target="_blank">Datasheet</a></li></ul></div>                    </div>
		        
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				        <h3>Selected References</h3><ol class="prod-ref_list"><li>Couradeau, E., <em>et al.</em> (2019). Probing the active fraction of soil microbiomes using BONCAT-FACS <em>Nat Commun,</em> <strong>10</strong>, 2770-80. [<a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591230/" target="_blank" rel="noopener">PubMed</a>]</li></ol>                    </div>
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		<p>The post <a rel="nofollow" href="https://staging.vectorlabs.com/products/l-homopropargylglycine-hpg/">L-Homopropargylglycine (HPG)</a> appeared first on <a rel="nofollow" href="https://staging.vectorlabs.com">VectorLabs</a>.</p>
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		<title>L-Azidohomoalanine (AHA)</title>
		<link>https://staging.vectorlabs.com/products/l-azidohomoalanine-aha/</link>
		
		<dc:creator><![CDATA[Vector Laboratories R&D]]></dc:creator>
		<pubDate>Tue, 19 Sep 2023 19:15:26 +0000</pubDate>
				<guid isPermaLink="false">https://staging.vectorlabs.com/?post_type=product&#038;p=21748</guid>

					<description><![CDATA[<h3>Description</h3>
<p>L-Azidohomoalanine (AHA) is an amino acid analog of methionine that contains a very small modification, specifically an azido moiety that can be fed to cultured cells and incorporated into proteins during active protein synthesis. Detection utilizes the chemoselective ligation or “click ” reaction between an azide and an alkyne or cyclooctyne. The azido-modified protein is detected with either fluorescent alkyne or biotin alkyne. Detection sensitivity with these reagents in 1-D gels and Western blots is in the low femtomole range and compatible with downstream LC-MS⁄MS and MALDI MS analysis.</p>
<h3>Specifications</h3>
<table id="product-attribute-specs-table" class="data table additional-attributes" width="585">
<tbody>
<tr>
<th class="col label" scope="row">Unit Size</th>
<td class="col data" data-th="Unit Size">25 mg, 100 mg, 1000 mg, 5 g</td>
</tr>
<tr>
<th class="col label" scope="row">Molecular weight</th>
<td class="col data" data-th="Applications">180.59 (HCl salt)</td>
</tr>
<tr>
<th class="col label" scope="row">Chemical composition</th>
<td class="col data" data-th="Target Species">C4H9ClN4O2 (HCl salt)</td>
</tr>
<tr>
<th class="col label" scope="row">CAS</th>
<td class="col data" data-th="Conjugate">942518-29-8</td>
</tr>
<tr>
<th class="col label" scope="row">Solubility</th>
<td class="col data" data-th="Format">Water, DMSO, DMF</td>
</tr>
<tr>
<th class="col label" scope="row">Purity</th>
<td class="col data" data-th="Format">&#62;95% (H NMR)</td>
</tr>
<tr>
<th class="col label" scope="row">Appearance</th>
<td class="col data" data-th="Format">White crystalline</td>
</tr>
<tr>
<th class="col label" scope="row">Storage Conditions</th>
<td class="col data" data-th="Format">-20°C.</td>
</tr>
<tr>
<th class="col label" scope="row">Shipping Conditions</th>
<td class="col data" data-th="Format">Ambient temperature</td>
</tr>
</tbody>
</table>
<p>&#160;</p>
<p>The post <a rel="nofollow" href="https://staging.vectorlabs.com/products/l-azidohomoalanine-aha/">L-Azidohomoalanine (AHA)</a> appeared first on <a rel="nofollow" href="https://staging.vectorlabs.com">VectorLabs</a>.</p>
]]></description>
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                                                            <h2 class="eael-tab-title title-after-icon" >Description</h2>                                                    </li>
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                                                            <h2 class="eael-tab-title title-after-icon" >Specifications</h2>                                                    </li>
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                                                            <h2 class="eael-tab-title title-after-icon" >Selected References</h2>                                                    </li>
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                    <div id="description-tab" class="clearfix eael-tab-content-item inactive" data-title-link="description-tab">
				        <h3>Description</h3><p>L-Azidohomoalanine (AHA) is an amino acid analog of methionine that contains a very small modification, specifically an azido moiety that can be fed to cultured cells and incorporated into proteins during active protein synthesis. Detection utilizes the chemoselective ligation or “click ” reaction between an azide and an alkyne or cyclooctyne. The azido-modified protein is detected with either fluorescent alkyne or biotin alkyne. Detection sensitivity with these reagents in 1-D gels and Western blots is in the low femtomole range and compatible with downstream LC-MS⁄MS and MALDI MS analysis.</p>                    </div>
		        
                    <div id="specifications-tab" class="clearfix eael-tab-content-item inactive" data-title-link="specifications-tab">
				        <h3>Specifications</h3><table id="product-attribute-specs-table" class="data table additional-attributes" style="height: 186px;" width="585"><tbody><tr><th class="col label" scope="row">Unit Size</th><td class="col data" data-th="Unit Size">25 mg, 100 mg, 1000 mg, 5 g</td></tr><tr><th class="col label" scope="row">Molecular weight</th><td class="col data" data-th="Applications">180.59 (HCl salt)</td></tr><tr><th class="col label" scope="row">Chemical composition</th><td class="col data" data-th="Target Species">C4H9ClN4O2 (HCl salt)</td></tr><tr><th class="col label" scope="row">CAS</th><td class="col data" data-th="Conjugate">942518-29-8</td></tr><tr><th class="col label" scope="row">Solubility</th><td class="col data" data-th="Format">Water, DMSO, DMF</td></tr><tr><th class="col label" scope="row">Purity</th><td class="col data" data-th="Format">&gt;95% (H NMR)</td></tr><tr><th class="col label" scope="row">Appearance</th><td class="col data" data-th="Format">White crystalline</td></tr><tr><th class="col label" scope="row">Storage Conditions</th><td class="col data" data-th="Format">-20°C.</td></tr><tr><th class="col label" scope="row">Shipping Conditions</th><td class="col data" data-th="Format">Ambient temperature</td></tr></tbody></table>                    </div>
		        
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				        <h3>Documents</h3><div class="explorer_section applications container documentSection catalog-product-document"><ul class="document_list"><li class="documentContainer documentItem"><a class="documentTitle" href="https://staging.vectorlabs.com/productattachments/sds/VL_CCT-1066_sds.pdf">Safety Data Sheet</a></li><li><a href="https://staging.vectorlabs.com/resources/certificate-of-analysis/">Download CoA</a></li><li><a class="woocommerce-print-products-pdf-link" href="https://staging.vectorlabs.com/products/l-azidohomoalanine-aha/?print-products=pdf" target="_blank">Datasheet</a></li></ul></div>                    </div>
		        
                    <div id="selected-references-tab" class="clearfix eael-tab-content-item inactive" data-title-link="selected-references-tab">
				        <h3>Selected References</h3><div class="product-tab"><div class="tab-content"><div id="tab-second_tab_content" class="tab-pane fade woocommerce-Tabs-panel--second_tab_content active show" role="tabpanel" aria-labelledby="tab-title-second_tab_content"><ol class="prod-ref_list"><li>Loebel , C., <em>et al.</em> (2022). Metabolic labeling of secreted matrix to investigate cell-material interactions in tissue engineering and mechanobiology. <em>Nat Protoc.</em>, <strong>10.1038</strong>, Online ahead of print. [<a href="https://pubmed.ncbi.nlm.nih.gov/35140408/" target="_blank" rel="noopener">PubMed</a>]</li><li>Bruna, R. E., <em>et al.</em> (2021). Limitation of phosphate assimilation maintains cytoplasmic magnesium homeostasis. <em>Proc Natl Acad Sci U S A.</em>, <strong>118 (11)</strong>, e2021370118. [<a href="https://pubmed.ncbi.nlm.nih.gov/33707210/" target="_blank" rel="noopener">PubMed</a>]</li><li>Costello, A., <em>et al.</em> (2021). Directed evolution of rRNA improves translation kinetics and recombinant protein yield. <em>Nat Commun.</em>, <strong>12 (1)</strong>, 5638. [<a href="https://pubmed.ncbi.nlm.nih.gov/34561441/" target="_blank" rel="noopener">PubMed</a>]</li><li>Kwong, J. Q., <em>et al.</em> (2021). Mitochondrial functional resilience after TFAM ablation in the adult heart. <em>Am J Physiol Cell Physiol.</em>, <strong>320 (6)</strong>, C929-C942. [<a href="https://pubmed.ncbi.nlm.nih.gov/33760663/" target="_blank" rel="noopener">PubMed</a>]</li><li>Heybrock, S., <em>et al.</em> (2021). S-palmitoylation determines TMEM55B-dependent positioning of lysosomes. <em>J Cell Sci.</em>, <strong>135 (5)</strong>, jcs258566. [<a href="https://pubmed.ncbi.nlm.nih.gov/34350967/" target="_blank" rel="noopener">PubMed</a>]</li><li>Coates, H. W. <em>et al.</em> (2021). The mammalian cholesterol synthesis enzyme squalene monooxygenase is proteasomally truncated to a constitutively active form. <em>J Biol Chem.</em>, Online ahead of print. [<a href="https://pubmed.ncbi.nlm.nih.gov/33933449/" target="_blank" rel="noopener">PubMed</a>]</li><li>Morral, C., <em>et al.</em> (2020). Zonation of Ribosomal DNA Transcription Defines a Stem Cell Hierarchy in Colorectal Cancer. <em>Cell Stem Cell.</em>, <strong>26 (6)</strong>, 845-861.e12. [<a href="https://pubmed.ncbi.nlm.nih.gov/32396863/" target="_blank" rel="noopener">PubMed</a>]</li><li>Smeekens, J. M., <em>et al.</em> (2020). Systematic quantification of the dynamics of newly synthesized proteins unveiling their degradation pathways in human cells. <em>Chem Sci.</em>, <strong>11 (13)</strong>, 3557-3568. [<a href="https://pubmed.ncbi.nlm.nih.gov/34109028/" target="_blank" rel="noopener">PubMed</a>]</li><li>Tao, W.A., <em>et al.</em> (2019). Identification and Quantification of Newly Synthesized Proteins Using Mass Spectrometry‐Based Chemical Proteomics. <em>Mass Spectrometry‐Based Chemical Proteomics. </em>[<a href="https://onlinelibrary.wiley.com/doi/abs/10.1002/9781118970195.ch8" target="_blank" rel="noopener">PubMed</a>]</li><li>Dumont, A. A., <em>et al.</em> (2018). ADAP1 limits neonatal cardiomyocyte hypertrophy by reducing integrin cell surface expression. <em>Sci Rep.</em>, <strong>8 (1)</strong>, 13605. [<a href="https://pubmed.ncbi.nlm.nih.gov/30206251/" target="_blank" rel="noopener">PubMed</a>]</li></ol></div></div></div>                    </div>
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