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MSH6 antibody

The Mouse Monoclonal anti-MSH6 antibody (Clone 3A10H7) (ABIN931485) specifically detects MSH6 in WB and ELISA. The antibody is reactive with Human samples.
Catalog No. ABIN931485
$1,458.04
Plus shipping costs $50.00
100 μL
Shipping to: United States
Delivery in 16 to 22 Business Days

Quick Overview for MSH6 antibody (ABIN931485)

Target

See all MSH6 Antibodies
MSH6 (MutS Homolog 6 (E. Coli) (MSH6))

Reactivity

  • 207
  • 57
  • 52
  • 8
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 119
  • 85
  • 3
Mouse

Clonality

  • 156
  • 50
  • 1
Monoclonal

Conjugate

  • 124
  • 10
  • 5
  • 5
  • 5
  • 5
  • 5
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MSH6 antibody is un-conjugated

Application

  • 140
  • 103
  • 80
  • 49
  • 48
  • 32
  • 29
  • 19
  • 14
  • 13
  • 8
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA

Clone

3A10H7
  • Immunogen

    MSH6 antibody was raised in Mouse using a purified recombinant fragment of MSH6 expressed in E. coli as the immunogen.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1:10,000, WB: 1:500-1:2000
    Optimal conditions should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    Lot specific

    Buffer

    Supplied as a liquid in ascitic fluid containing 0.03 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium Azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 4 °C for short term storage. Store at -20 °C for long term storage.
  • Target

    MSH6 (MutS Homolog 6 (E. Coli) (MSH6))

    Alternative Name

    MSH6

    Background

    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. Synonyms: Monoclonal MSH6 antibody, Anti-MSH6 antibody, Muts Homolog 6 antibody, GTBP antibody, HNPCC5 antibody, HSAP antibody.

    Pathways

    DNA Damage Repair, Chromatin Binding, Production of Molecular Mediator of Immune Response
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