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Merck
CN

KEM0004

Sigma-Aldrich

Exonuclease III

Ultra-pure enzyme for nucleic acid modifications

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等级

Molecular Biology

方案

>99% (SDS-PAGE)

表单

buffered aqueous solution

比活

100,000 U/mg

浓度

100,000 U/mL

运输

dry ice

储存温度

−20°C

一般描述

Exonuclease III is a 3′ → 5′ exonuclease which acts by digesting one strand of a dsDNA duplex at a time or digesting the RNA strand of an RNA-DNA heteroduplex. Exonuclease III breaks phosphodiester bonds on the 5′ side of AP sites in both dsDNA and ssDNA, removes 3′ terminal groups on dsDNA, increases MutY turnover, and efficiently degrades 3′ recessed but not 3′ protruding DNA ends (creating 5′ overhangs). Exo III removes a limited number of nucleotides per binding event, resulting in coordinated progressive deletions within the population of DNA molecules.

应用

Suitable for removal of nucleotide(s) from duplex DNA in 3′ – 5′ direction.

特点和优势

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

外形

Supplied in 25 mM Tris-HCl, 50 mM KCl, 1.0 mM DTT, 0.1 mM EDTA and 50% glycerol at pH 8.0 @ 25° C.

其他说明

1 unit is defined as the amount of enzyme required to produce 1 nmol of acid-soluble total nucleotide in 30 minutes at 37° C.
Source of protein: Purified from a strain of E. coli that expresses the recombinant Exonuclease III gene.
Supplied with:KEM0004B (10X Yellow Buffer)
Unit size: 50,000 U

储存分类代码

10 - Combustible liquids

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

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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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