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	<title>RT05 &#8211; Tinzyme</title>
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	<description>Enzymes, dNTP and rNTP</description>
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		<title>HiFi II MMLV Reverse Transcriptase (RNase H-)</title>
		<link>https://www.tinzyme.com/rt-pcr/hifi-ii-mmlv-reverse-transcriptase-rnase-h/</link>
		
		<dc:creator><![CDATA[tinzyme]]></dc:creator>
		<pubDate>Fri, 03 Jan 2025 02:00:07 +0000</pubDate>
				<category><![CDATA[RT PCR]]></category>
		<category><![CDATA[MMLV]]></category>
		<category><![CDATA[RT05]]></category>
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					<description><![CDATA[RT05-HiFi II M-MLV Reverse Transcriptase (RNase H-...]]></description>
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<p><a href="https://www.tinzyme.com/man/RT05.pdf" data-type="link" data-id="https://www.tinzyme.com/man/RT05.pdf" target="_blank" rel="noreferrer noopener">Manual</a></p>



<p><strong>Product Number: </strong><strong>RT05</strong><strong></strong></p>



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



<p>-20°C</p>



<p><strong>Components</strong></p>



<figure class="wp-block-table"><table class="has-fixed-layout"><tbody><tr><td>Component</td><td>RT05 10000U</td></tr><tr><td>HiFi II M-MLV(H-) (200U /μL) 5×SuperRT Buffer</td><td>50 μL 1 mL</td></tr></tbody></table></figure>



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



<p>HiFi II M-MLV(H-) is a reverse transcription enzyme in which the mutant M-MLV gene is recombined and expressed by Escherichia coli engineering bacteria. The enzyme can catalyze the polymerization of complementary DNA using RNA or DNA: RNA hybrid chain as template. The mutation of HiFi II M-MLV reverse transcriptase RNase H activity is lost, reducing the degradation of RNA in reverse transcription and facilitating the acquisition of full-length cDNA. HiFi II M-MLV reverse transcriptase can synthesize the first strand cDNA at 55°C, providing higher specificity and stability, and can synthesize up to 12 KB cDNA with high cDNA yield. It is suitable for synthesis of first strand cDNA, RT-PCR, RT-QPCR and construction of full-length cDNA library.</p>



<p><strong>Activity Definition</strong></p>



<p>Using Poly (A) as template and Oligo (dT) as primer, the amount of enzyme required for catalytic incorporation of 1 nmol dTTP within 10 minutes was defined as an activity unit (U) at 37°C.</p>



<p><strong>Quality Control</strong></p>



<p>The electrophoretic bands of RNA did not change after the reaction of 200 U of this enzyme with 1 μg of 16 S and 23 S rRNA at 37°C for 1 hour.</p>
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