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|Tested species reactivity||Human|
|Host / Isotype||Mouse / IgG1|
|Immunogen||Fusion protein derived from human muscle.|
|Storage buffer||PBS, pH 7.4, with 1% BSA|
|Contains||0.1% sodium azide|
|Storage Conditions||4° C|
|Tested Applications||Dilution *|
|Immunohistochemistry (Paraffin) (IHC (P))||Assay Dependent|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
Defects in MSH6 are a cause of hereditary non-polyposis colorectal cancer (HNPCC) (Lynch syndrome). HNPCC is an autosomal, dominantly inherited disease associated with marked increase in cancer susceptibility. it is characterized by a familial predisposition to early onset colorectal carcinoma (crc) and extra-colonic cancers of the gastrointestinal, urological and female reproductive tracts. HNPCC is reported to be the most common form of inherited colorectal cancer in the western world. MSH6 is central to mismatch DNA repair.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
G/T mismatch-binding protein; GTBP; GTMBP; MSH6; mutS-alpha 160 kDa subunit; p160; sperm-associated protein
GTBP; GTMBP; HNPCC5; HSAP; MSH6; p160