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Merck
CN

KEM0015

Sigma-Aldrich

RNAse H

Ultra-pure enzyme for nucleic acid modifications

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Molecular Biology

Assay

>99% (SDS-PAGE)

form

buffered aqueous solution

specific activity

625,000 U/mg

concentration

5,000 U/mL

shipped in

dry ice

storage temp.

−20°C

General description

E. coli RNAse H (rnh) is an endoribonuclease which degrades the RNA strand of RNA/DNA hybrid molecules. RNAse H digestion produces ribonucleotide molecules with 5′-phosphate and 3′-hydroxyl termini. RNAse H is nearly inactive against single or double-stranded RNA molecules.

Application

Suitable for:
  • Cleavage of RNA strand of a DNA:RNA hybrid
  • Removing mRNA during second strand cDNA synthesis

Features and Benefits

  • Ultra-purification process for ultimate enzyme performance
  • Highest quality specifications for ultimate product consistency
  • Undetectable DNA and nuclease contamination

Physical form

Supplied in 20 mM Tris-HCl, 100 mM KCl, 10 mM MgCl2, 0.1 mM EDTA, 0.1 mM DTT and 50% glycerol at pH @ 25° C.

Other Notes

1 unit is defined as the amount of enzyme that will hydrolyze 1 nmol of RNA from an 3H-labeled DNA:RNA hybrid molecule into acid-soluble material in 20 minutes at 37° C.
Source of protein: A recombinant E.coli strain carrying the RNAse H (rnh) gene.
Supplied with:KEM0015 B (10X RNAse H Buffer)
Unit size: 5,000 U

Pictograms

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Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

Regulatory Information

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Laure Rittié et al.
Journal of cell communication and signaling, 2(1-2), 25-45 (2008-09-04)
Since molecular cloning has become routine laboratory technique, manufacturers offer countless sources of enzymes to generate and manipulate nucleic acids. Thus, selecting the appropriate enzyme for a specific task may seem difficult to the novice. This review aims at providing

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