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.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=32-196
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
Curated Selection
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