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RAD51C antibody (AA 1-135)

This Rabbit Polyclonal antibody specifically detects RAD51C in IF. It exhibits reactivity toward Human.
Catalog No. ABIN6146644

Quick Overview for RAD51C antibody (AA 1-135) (ABIN6146644)

Target

See all RAD51C Antibodies
RAD51C (DNA Repair Protein RAD51 Homolog 3 (RAD51C))

Reactivity

  • 39
  • 4
  • 2
  • 2
Human

Host

  • 32
  • 6
  • 1
Rabbit

Clonality

  • 34
  • 5
Polyclonal

Conjugate

  • 27
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This RAD51C antibody is un-conjugated

Application

  • 31
  • 19
  • 11
  • 7
  • 2
  • 2
  • 2
  • 1
  • 1
Immunofluorescence (IF)
  • Binding Specificity

    • 9
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-135

    Sequence

    MRGKTFRFEM QRDLVSFPLS PAVRVKLVSA GFQTAEELLE VKPSELSKEV GISKAEALET LQIIRRECLT NKPRYAGTSE SHKKCTALEL LEQEHTQGFI ITFCSALDDI LGGGVPLMKT TEICGAPGVG KTQLW

    Cross-Reactivity

    Human

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-135 of human RAD51C (NP_002867.1).

    Isotype

    IgG
  • Application Notes

    IF,1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    RAD51C (DNA Repair Protein RAD51 Homolog 3 (RAD51C))

    Alternative Name

    RAD51C

    Background

    This gene is a member of the RAD51 family. RAD51 family members are highly similar to bacterial RecA and Saccharomyces cerevisiae Rad51 and are known to be involved in the homologous recombination and repair of DNA. This protein can interact with other RAD51 paralogs and is reported to be important for Holliday junction resolution. Mutations in this gene are associated with Fanconi anemia-like syndrome. This gene is one of four localized to a region of chromosome 17q23 where amplification occurs frequently in breast tumors. Overexpression of the four genes during amplification has been observed and suggests a possible role in tumor progression. Alternative splicing results in multiple transcript variants.,RAD51C,BROVCA3,FANCO,R51H3,RAD51L2,Epigenetics & Nuclear Signaling,DNA Damage & Repair,RAD51C

    Molecular Weight

    14 kDa/42 kDa

    Gene ID

    5889

    UniProt

    O43502

    Pathways

    DNA Damage Repair
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