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        <h1 class="post-title" style="">Ribonuclease H (RNase H)</h1>
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                            <span>Last updated on 2026-10-12</span>
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                        <img alt='surzyme' src='https://weavatar.com/avatar/af42555338bd02899f2f4c80494cf4fc9a3a807f2521d66cbd4749b27b995a25?s=24&#038;d=mm&#038;r=g' srcset='https://weavatar.com/avatar/af42555338bd02899f2f4c80494cf4fc9a3a807f2521d66cbd4749b27b995a25?s=48&#038;d=mm&#038;r=g 2x' class='avatar avatar-24 photo avatar-small' height='24' width='24' loading='lazy' decoding='async'/>                        surzyme                    </span>
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<p class="wp-block-paragraph">Ribonuclease H (RNase H) is an endoribonuclease that specifically degrades the RNA strand in RNA-DNA hybrids, generating 5´-phosphate-terminated oligoribonucleotides and single-stranded DNA.<br><br>Applications<br>Removal of mRNA during second-strand cDNA synthesis. Removal of poly(A) sequences from mRNA in the presence of Oligo(dT). Oligodeoxynucleotide-mediated RNA cleavage.<br><br>Source<br>Fermented and purified from recombinant <em>Escherichia coli</em>.<br><br>Performance and Quality Control<br>Tested for ribonuclease, non-specific deoxyribonuclease, 3´ and 5´ deoxyriboexonuclease activities.<br><br>Unit Definition<br>One unit is defined as the amount of enzyme that hydrolyzes 1 nmol of RNA in <sup>3</sup>H-labeled poly(A)·poly(dT) into acid-soluble material within 20 min at 37°C.<br><br>Unit Assay Conditions<br>20 mM Tris-HCl (pH 7.5), 0.1 M KCl, 10 mM MgCl<sub>2</sub>, 0.1 mM DTT, 5% (w/v) sucrose, 0.5 nmol <sup>3</sup>H-labeled poly(A)·poly(dT) and 50 µL enzyme, incubated at 37°C for 20 min.</p>

