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MSH2 Antibody [3A2B8C]

Product Specifications

Background

MSH2 is a 100 kDa nuclear antigen and encodes a protein of 934 amino acids. The MSH2 gene is one of 4 known genes encoding proteins involved in the repair of mismatch nucleotides following DNA replication or repair. Mutations in the MSH2 gene contribute to the development of sporadic colorectal carcinoma. MSHS mutations are responsible for 50% of inherited non-polyposis colorectal (HNPCC) . The repair of mismatch DNA is essential to maintaining the integrity of genetic information over time. An alteration of microsatellite repeats is the result of slippage owing to strand misalignment during DNA replication and is referred to as microsatellite instability (MSI) . These defects in DNA repair pathways have been related to human carcinogenesis. MSH-2 is involved in the initial cognition of mismatch nucleotides during the replication mismatch repair process.

NCBI Gene ID

4436

Swiss Prot

P43246

Accession Number

P43246

Host

Mouse

Reactivity

Human

Immunogen

Ni-NTA purified recombinant human MSH2 expressed in E. Coli strain BL21 (DE3) .

Clonality

Monoclonal

Clone

3A2B8C

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Other

Concentration

Batch dependent

Buffer

Ascitic fluid containing 0.03% sodium azide.

Modification

None

Shipping Conditions

Blue Ice

Storage Conditions

MSH2 monoclonal antibody can be stored at -20˚ C, stable for one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Fragment

IgG1

Symbol

MSH2

NCBI Official Name

MutS homolog 2

NCBI Organism

Homo sapiens

Background Reference 01

Papadopoulos, N. 1994. Science 263: 1625-1629.

Background Reference 02

Palombo, F. 1994. Nature 367:417-418.

Other Product Names

MutS protein homolog 2, hMSH2, FCC1, COCA1, HNPCC, LCFS2, HNPCC1

Tested Applications

ELISA, WB, IHC

Protein ID

1171032

Frequently Asked Questions

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