MutS Protein (Thermus aquaticus)

$0.00$2,181.03

The MutS DNA mismatch protein recognizes heteroduplex DNAs containing mispaired or unpaired bases.

SKU: SKU49548 Categories: ,
SKU OPTIONS PriceQuantity
MUTST-100 100 ug (1 mg/ml) $311.58
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MUTST -200 1 mg (1 mg/ml) $2,181.03
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MUTST -OEM Any size Please inquire
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Description

Description:
The MutS DNA mismatch protein recognizes heteroduplex DNAs containing mispaired or unpaired bases. This Muts protein binds in vitro to heteroduplex DNAs containing mispaired or unpaired bases over a wide temperature range from 4 to 70 °C and has a thermostable ATPase activity. This thermostable Taq MutS is active at temperature between 0 to 75°C. Since Taq MutS efficiently binds to 1-4 bases deletion (or insertion) and mismatch base pairs, it is useful for detecting these mutations. Mutations can be detected in polyacrylamide gels or on a solid phase such as Ni agarose or beads or magnetic Ni-NTA particles.

Applications:
• Remove mismatch DNA (error correction) from gene synthesis reaction
• Mutation detection and removal
• Rapid isothermal SNP detection

Full name:
Thermus aquaticus MutS DNA mismatch repair protein

Source:
expressed in E. coli

Fusion Tag:
6XHis tag at C-terminus

Accession #:
AAC43637

Molecule Weight:
92.8 kDa

Purity:
> 98 % as determined by SDS-PAGE

Storage Buffer:
20 mM Tris-HCl, pH 8.0, 250 mM NaCl, 0.1mM EDTA, 1 mM DTT, 50% Glycerol

Reaction Buffer:
100mM KCl, 50 mM Tris-HCl, pH 8.5, 10 mM MgCl2, 0.1 mM EDTA, 1 mM DTT, 2% Glycerol, 65 °C

Storage:
-20°C Avoid repeated freeze-thaw cycles.

References:

1. Protein-mediated error correction for de novo DNA synthesis. Nucleic Acids Res. 2004 Nov 23;32(20):e162.

2. Correcting errors in synthetic DNA through consensus shuffling. Nucleic Acids Res. 2005 Mar 30;33(6):e55.

3. MutS as a tool for mutation detection. Acta Biochim Pol. 2005;52(3):575-83. Epub 2005 Aug 4.

4. One tube mutation detection using sensitive fluorescent dyeing of MutS protected DNA. Nucleic Acids Res. 2000 Apr 15;28(8):E36.

5. Rapid SNP diagnostics using asymmetric isothermal amplification and a new mismatch-suppression technology. Nature Methods – 4, 257 – 262 (2007) doi:10.1038/nmeth1007

Additional information

OPTIONS

100 ug (1 mg/ml), 1 mg (1 mg/ml), Any size

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