SKU: 29048665280

RNase Ⅲ

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Description

RNase ⅢProduct Specification Synonyms Ribonuclease 3,Ribonuclease III,RNase III Amino Acid Sequence Molecular Weight 70 kD Purity 95% by SDS PAGE Conjugation Unconjugated Physical Appearance Liquid Storage Buffer 500 mM NaCl10 mM Tris HCl0. 5 mM EDTA1 mM DTT50% Glycerol pH 8 @ 25C Reconstitution Stability & Storage Store at 25 ~ 15 for 2 years Reference [1] Nicholson AW. Ribonuclease III mechanisms of double stranded RNA cleavage. Wiley Interdiscip Rev RNA.

Product Specification


Synonyms Ribonuclease 3,Ribonuclease III,RNase III
Amino Acid Sequence

/

Molecular Weight

70 kD

Purity >95% by SDS-PAGE
Conjugation Unconjugated
Physical Appearance Liquid
Storage Buffer 500 mM NaCl、10 mM Tris-HCl、0.5 mM EDTA、1 mM DTT、50% Glycerol (pH 8 @ 25°C)
Reconstitution

/

Stability & Storage

Store at -25 ~ -15℃ for 2 years

Reference

[1] Nicholson AW. Ribonuclease III mechanisms of double-stranded RNA cleavage. Wiley Interdiscip Rev RNA. 2014 Jan-Feb;5(1):31-48. [2] Wu CX, Xu XJ, Zheng K, Liu F, Yang XD, Chen CF, Chen HC, Liu ZF. Characterization of ribonuclease III from Brucella. Gene. 2016 Apr 1;579(2):183-92. [3] Sun, Weimei et al. Catalytic mechanism of Escherichia coli ribonuclease III: kinetic and inhibitor evidence for the involvement of two magnesium ions in RNA phosphodiester hydrolysis. Nucleic Acids Research 33 (2005): 807 - 815.

Background

The processing of double-stranded(ds) RNA by RNase III family members is an essential step in the maturation and decay of coding and noncoding RNAs, including miRNAs and siRNAs. RNase III family members share a unique fold (RNase III domain) that can dimerize to form a structure that binds dsRNA and cleaves phosphodiesters on each strand, providing the characteristic 2 nt, 3'-overhang product ends. RNase III converts long double-stranded RNA into a heterogeneous mix of short (18–25 bp) interfering RNAs (siRNA).

Components

Storage Solution: 2U/μl RNase Ⅲ、500 mM NaCl、10 mM Tris-HCl、0.5 mM EDTA、1 mM DTT、50% Glycerol(pH 8 @ 25°C) 10*Reaction Buffer: 500 mM Tris-HCl、1 mM DTT 50 mM NaCl (pH 7.5 @ 25°C) 10*EDTA: 500 mM 10*MnCl2: 200 mM

Protocol

Set-up a typical reaction as follows 1)Add the following components in sequence 2)Incubate at 37°C for 20 minutes This reaction can be scaled up according to experimental needs.

Guidelines

Please avoid repeated freeze-thaw cycles.

Unit Definition

One unit is the amount of enzyme required to digest 1 μg of dsRNA to siRNA in 20 minutes at 37°C in a total reaction volume of 50 μl.
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SKU: 29048665280

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