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 - RTULCR-0640-06
Catalog number - Conc.LCM-0640-1.0
Antibody typeRabbit monoclonal antibody
CloneRED2
Cellular localizationNucleus
Positive controlTonsils
Antigen retrievingCitrate
CertificationsHealth Canada, IVD CE