RNase H2
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RNase H2 is the predominant source of RNase H activity in mammalian and human cells. RNase H2 protects genome integrity. RNase H2 has been associated with ribonucleotide removal from genomic DNA in yeast and mouse, where it is required for embryonic development.
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
Description
In Vitro
Product Information
This product is recombinantly expressed in E. coli. In addition to degrading the RNA chain in the R-loop and DNA-RNA complex chain, it can also specifically cut single ribonucleotides in the DNA double-stranded chain to repair the DNA double-stranded chain.
Storage buffer: 20 mM Tris-HCl, 100 mM KCI, 1 mM DTT, 1 mM EDTA, 50% Glycerol, pH 8.0
Instructions
1. Add 100 pmol double-stranded DNA substrate, 0.2-0.5 μL RNase H2, 5 μL reaction buffer (200 mM Tris-HCl, 100 mM (NH4) 2SO4, 100 mM KCl, 20 mM MgSO4, 1% Triton X-100, pH 8.8) according to the reaction system, and add Nuclease-free Water to make up to 50 μL;
2. After mixing, incubate the sample at 37°C for 30 min.
| Specification | Type | Components | Volume | Quantity |
| 100 U | A | RNase H2 | 100 U | 1 |
| 100 U | B | 10x RNase H2 Reaction Buffer | 200 μL | 2 |
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
EC Number
3.1.26.4
Enzyme Activity
>5 U/μl
Unit Definition
One unit is defined as the amount of enzyme that can cleave 1 nmol of synthetic DNA/RNA hybrid double-stranded body substrate containing a single R-loop per min at 37°C
Chemical Information
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Appearance Liquid
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Color Colorless to light yellow
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SMILES
[RNase H2]
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocole
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Protocol for Southern Blot
Southern blot is a DNA hybridization assay used to detect a defined DNA sequence within restriction-digested or otherwise fragmented genomic DNA. The method separates DNA fragments by agarose gel electrophoresis, transfers the size-resolved DNA pattern onto a solid support, denatures the DNA to permit base pairing, and detects fragments that hybridize with a complementary labeled probe; the readout is a band, smear, or fragment-size distribution corresponding to the target sequence and its restriction-fragment context. The assay reflects sequence presence, restriction fragment length, gene copy pattern, structural rearrangement, insertion or deletion affecting restriction sites, and some repeat-length or terminal restriction fragment applications when the experimental design links the probe to those genomic features. Classic applications include Southern blot-based telomere terminal restriction fragment analysis and minisatellite-based DNA fingerprinting, which illustrate how the same
Pureté et documentation
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Fiche technique (268 KB)
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SDS (251 KB)
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Instruction de manipulation (2659 KB)
Références
[1]. Feng S, Cao Z. Is the role of human RNase H2 restricted to its enzyme activity? Prog Biophys Mol Biol. 2016 May;121(1):66-73. [Content Brief]
[2]. Chon H, et al. RNase H2 roles in genome integrity revealed by unlinking its activities. Nucleic Acids Res. 2013 Mar 1;41(5):3130-43. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)