Progen Matériel de laboratoire

Description

MSH2 is a rabbit monoclonal antibody for immunohistochemistry from Bio SB. MSH2 is a mismatch repair gene commonly associated with Hereditary Non-Polyposis Colorectal Cancer (HNPCC). This gene was identified as a locus frequently mutated in HNPCC. When cloned, it is a human homolog of the E. coli DNA mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. MSH2 is abnormally deficient in a high proportion of patients with microsatellite instability (MSI-H). This finding is associated with the autosomal dominant condition found in Hereditary Non-Polyposis Colon Cancer. This anti-MSH2 antibody (along with MLH1 antibody) is useful in screening patients and families for this rare condition. Colon cancers that are microsatellite unstable have a better prognosis than their microsatellite stable counterparts.

Synonymes

COCA1, DNA mismatch repair protein Msh2, FCC1, hMSH2, HNPCC, HNPCC1, homolog 2 colon cancer nonpolyposis type 1 E coli, MutS protein homolog 2, msh-2, anti-msh2, anti-msh-2, anti-msh-2, anti msh2, anti msh-2, anti msh 2

Caractéristiques

Type
Rabbit Monoclonal
Clone
RBT-MSH2
Isotype
IgG
Réactivité
Paraffin, Frozen
Localisation
Nuclear
Contrôle
Colon Mucosa, Colon Carcinoma
Usage prévu
For In Vitro Diagnostic Use

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