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You are here:Home » Antibodies » Abs to Transcription Factors » Anti -MSH6 (MutS Homolog 6 (E. coli), DNA Mismatch Repair Protein MSH6, G/T Mismatch Binding Protein, GTBP, GTMBP, Hereditary Nonpolyposis Colorectal Cancer Type 5, HNPCC5, MutS alpha 160kD Subunit, p160, Sperm Associated Protein, hSAP)

Anti -MSH6 (MutS Homolog 6 (E. coli), DNA Mismatch Repair Protein MSH6, G/T Mismatch
Binding Protein, GTBP, GTMBP, Hereditary Nonpolyposis Colorectal Cancer Type 5, HNPCC5,
MutS alpha 160kD Subunit, p160, Sperm Associated Protein, hSAP)

Pricing

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Specifications

Clone Host Grade Applications
Monoclonal Mouse Affinity Purified IH
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. The MSH2-MSH6 complex recognizes a single-based mispair insertion/deletion loop. An alteration of microsatellite repeats is the result of slippage owing to strand misalignment during DNA replication and is referred to as microsatellite instability (MSI). These defects in DNA repair pathways have been related human carcinogenesis. Studies have shown the mutations of MLH-1, MSH2 and MSH6 genes contribute to the development of sporadic colorectal carcinoma. The repair of mismatch DNA is essential to maintaining the integrity of genetic information over time.
Catalog #M4692-36F
ApplicationsSuitable for use in Immunohistochemistry. Other applications not tested.
Recommended DilutionsImmunohistochemistry (paraffin): Neat
Optimal dilutions to be determined by the researcher.
Positive ControlTonsil, colon carcinoma
Storage and StabilityMay be stored at 4°C. For long-term storage, aliquot and store at 4°C. Do not freeze. Aliquots are stable for 12 months. For maximum recovery of product, centrifuge the original vial prior to removing the cap. Further dilutions can be made in assay buffer.
Clone TypeMonoclonal
IsotypeIgG1
Clone No8L806
HostMouse
SourceHuman
ConcentrationNot Determined
FormSupplied as a liquid in PBS, pH 7.5, sodium azide, BSA, 6M Urea.
PurityPurified by Protein G affinity chromatography.
ImmunogenSynthetic peptide corresponding to human MSH6. Cellular Localization: Nuclear.
SpecificityRecognizes human MSH6. MSH6 is a heterodimer of MSH2 and binds to DNA containing G/T mismatches.
Species CrossreactivityMouse, rat and canine
Important NoteThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.


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