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MSH6 (3A10) Antibody
ABBIOTEC

Supplier:

ABBIOTEC

Cat no: 252761

MSH6 (3A10) Antibody

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.\r

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SPECIFICATIONS

Catalog Number

252761

Size

0.1 ml

Applications

WB

Reactivities

Hum

Format

Each vial contains 0.1 ml ascitic fluid with 0.03% sodium azide.

P Type

Mouse Monoclonal Antibody

Antigen

Purified recombinant fragment of MSH6 e, Xenopus/Amphibian,pressed in E. coli. \r<br>

Isotype

Mouse IgG1

Accession

P52701

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

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