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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 |
Recommended dilutions |
100-200x |
Certifications |
Health Canada, IVD CE |
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