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MSH2 gene expression occurs in sporadic colorectal cancers. MSH2 gene mutations are associated with approximately 50% of familial and non-familial polyposis colorectal cancer (HNPCC). At present, it is mostly used together with MLH1, MSH6 and PMS2 to determine the gene mutations of hereditary nonpolyposis colorectal cancer.

Catalog number - RTU

LCR-0640-06

Catalog number - Conc.

LCM-0640-1.0

Antibody type

Rabbit monoclonal antibody

Clone

RED2

Cellular localization

Nucleus

Positive control

Tonsils

Antigen retrieving

Citrate

Certifications

Health Canada, IVD CE

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