MSH6 (3A10) Antibody

Cat no: 252761

Supplier: ABBIOTEC

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Description
Additional Information

MSH6 (DNA mismatch repair protein Msh6) mutations 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 e, Xenopus/Amphibian,tra-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.

Catalogue number:	252761
Reactivities:	Human
Applications:	Western Blot
Size:	0.1 ml
Accession:	P52701
Antigen:	Purified recombinant fragment of MSH6 e, Xenopus/Amphibian,pressed in E. coli.
Format:	Each vial contains 0.1 ml ascitic fluid with 0.03% sodium azide.
P type:	Mouse Monoclonal Antibody
Isotype:	Mouse IgG1
Clonality:	3A10H7
Additional info:	DNA mismatch repair protein Msh6; hMSH6; G/T mismatch-binding protein; GTBP; GTMBP; MutS-alpha 160 kDa subunit; p160; HSAP; HNPCC5