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	<title>S120308 &#8211; Tinzyme</title>
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		<title>Lambda Exonuclease</title>
		<link>https://www.tinzyme.com/exonuclease/lambda-exonuclease/</link>
		
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		<pubDate>Tue, 07 Apr 2026 05:53:11 +0000</pubDate>
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		<category><![CDATA[S120308]]></category>
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					<description><![CDATA[S120308, Lambda Exonuclease. Lambda Exonuclease, a...]]></description>
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<p><a href="https://www.tinzyme.com/man/S120308.pdf" target="_blank" rel="noreferrer noopener">Manual</a></p>



<p><strong>Product Number: S120308</strong></p>



<p><strong>Shipping and Storage</strong></p>



<p>Wet ice transportation; -Stored at 20℃, with a validity period of 12 months.</p>



<p><strong>Component</strong></p>



<figure class="wp-block-table"><table class="has-fixed-layout"><tbody><tr><td>Component<strong></strong></td><td>1000U</td></tr><tr><td>Lambda Exonuclease</td><td>200μL</td></tr><tr><td>10×Reaction Buffer</td><td>1mL</td></tr></tbody></table></figure>



<p><strong>Description</strong></p>



<p>Lambda Exonuclease, also known as lambda Exonuclease or lambda exonuclease, is a 5 &#8216;-3&#8217; deoxyribonuclease derived from the exonuclease gene of lambda bacteriophages and recombinant expressed in Escherichia coli. It can specifically hydrolyze the 5 &#8216;end phosphorylated strand in double stranded DNA along the 5&#8217; -3 &#8216;direction, but has low enzymatic activity for single stranded DNA and non phosphorylated dsDNA at the 5&#8217; end, and cannot be digested from DNA cuts or gaps.</p>



<p><strong>Application</strong></p>



<p>Production of single stranded PCR products, analysis of DNA single stranded conformational polymorphism, rolling ring amplification, PCR product cloning, etc.</p>



<p><strong>Features</strong></p>



<ol class="wp-block-list">
<li><strong>Source:</strong> Derived from λ bacteriophage, recombinant expressed by Escherichia coli.</li>



<li><strong>Enzyme activity definition: </strong>The amount of enzyme required to hydrolyze 10nmol of acid soluble deoxyribonucleotide from a double stranded DNA substrate in a 50μL reaction system at 37℃ within 1 minute is defined as one enzyme activity unit.</li>



<li><strong>Purity and concentration:</strong> SDS-PAGE detection shows a purity of ≥ 95%; Endogenous nucleic acid residue&lt;1 pg/μL (qPCR detection); Enzyme activity is 5U/μL.</li>



<li><strong>Inactivation or inhibition:</strong> Incubate at 75℃ for 10 minutes to inactivate.</li>



<li><strong>Enzyme storage buffer:</strong> 25mM Tris HCl, 50mM NaCl, 1 mM DTT, 0.1mM EDTA, 50% Glycerol, pH 8.</li>



<li><strong>10</strong>×<strong>Reaction Buffer:</strong> 670mM Glycine-KOH, 25mM MgCl<sub>2</sub>, 500μg/mL BSA, pH 9.4.</li>
</ol>



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