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MSH6 antibody

This Rabbit Polyclonal antibody specifically detects MSH6 in WB, IHC and IF. It exhibits reactivity toward Human, Mouse and Monkey.
Catalog No. ABIN6989836

Quick Overview for MSH6 antibody (ABIN6989836)

Target

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

Reactivity

  • 108
  • 35
  • 26
  • 6
  • 3
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Monkey

Host

  • 59
  • 46
  • 3
Rabbit

Clonality

  • 62
  • 45
  • 1
Polyclonal

Conjugate

  • 52
  • 7
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MSH6 antibody is un-conjugated

Application

  • 74
  • 58
  • 37
  • 33
  • 27
  • 18
  • 14
  • 13
  • 10
  • 10
  • 8
  • 6
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  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Cross-Reactivity

    Human, Monkey, Mouse

    Purification

    Purified by Protein A.

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-290 of human MSH6 (NP_000170.1).

    Isotype

    IgG
  • Application Notes

    WB 1:300-5000
    IHC()
    IF()

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C for 12 months.

    Expiry Date

    12 months
  • Target

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

    Alternative Name

    MSH6

    Background

    Synonyms: MSH6,GTBP,GTMBP,HNPCC5,HSAP,p160

    Background: This gene encodes a member of the DNA mismatch repair MutS family. In E. coli, the MutS protein helps in the recognition of mismatched nucleotides prior to their repair. A highly conserved region of approximately 150 aa, called the Walker-A adenine nucleotide binding motif, exists in MutS homologs. The encoded protein heterodimerizes with MSH2 to form a mismatch recognition complex that functions as a bidirectional molecular switch that exchanges ADP and ATP as DNA mismatches are bound and dissociated. Mutations in this gene may be associated with hereditary nonpolyposis colon cancer, colorectal cancer, and endometrial cancer. Transcripts variants encoding different isoforms have been described.

    Gene ID

    2956

    UniProt

    P52701

    Pathways

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