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MSH2 Mouse anti-Human, Clone: UMAB259, liquid, UltraMAB™
SDP

Mouse Monoclonal Antibody

Supplier:  OriGene UM800149

Encompass_Preferred

Catalog No. 50-168-5423


May include imposed supplier surcharges.
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Description

Description

Germline mutations in human mismatch repair genes (hMSH2, hMSH6, hMLH1, hPMS2) account for majority of the hereditary non-polyposis colorectal carcinoma (HPNCC). CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations. These mutations cause a mismatch repair deficiency resulting in a mutator phenotype where the replication errors are not repaired. Microsatellites/simple repeatative sequences are prone to this type of replication errors and instability of these microsatellites correlates with the occurance of HPNCC. hMSH2 binds to another MutS homolog protein GTBP to form a heterodimeric complex called hMutSbeta, which binds to insertion/deletion loops in DNA.
Specifications

Specifications

MSH2
Monoclonal
Unconjugated
MSH2
COCA1, FCC1, HNPCC, HNPCC1, LCFS2
Mouse
Affinity Chromatography
RUO
4436
-20° C, Avoid Freeze/Thaw Cycles
Liquid
Immunohistochemistry (Paraffin)
UMAB259
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide
P43246
MSH2
Human recombit protein fragment corresponding to amino acids 1-304 of human MSH2 produced in E.coli.
100 μL
Primary
Human
Antibody
IgG2b
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