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FANCG antibody (C-Term)

The Rabbit Polyclonal anti-FANCG antibody has been validated for WB and IHC. It is suitable to detect FANCG in samples from Human.
Catalog No. ABIN2798702

Quick Overview for FANCG antibody (C-Term) (ABIN2798702)

Target

See all FANCG Antibodies
FANCG (Fanconi Anemia Complementation Group G (FANCG))

Reactivity

  • 64
  • 5
  • 2
Human

Host

  • 59
  • 4
  • 1
Rabbit

Clonality

  • 62
  • 2
Polyclonal

Conjugate

  • 25
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FANCG antibody is un-conjugated

Application

  • 56
  • 26
  • 26
  • 22
  • 12
  • 9
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 23
    • 15
    • 8
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    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 540-568, C-Term

    Purpose

    Rabbit Anti-Human FANCG (C-term) Antibody

    Immunogen

    This FANCG antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 540-568 amino acids from the C-terminal region of human FANCG.

    Isotype

    Ig Fraction
  • Application Notes

    Western Blot, Immunohistochemistry
    Recommended Dilutions
    WB: 1:1000, IHC: 1:10-50FANCG Antibody (C-term) for immunohistochemistry. Clinical relevance has not been evaluated.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.500 mg/mL

    Storage

    4 °C,-20 °C

    Storage Comment

    2-8°C (short-term), -20°C (long-term)
  • Target

    FANCG (Fanconi Anemia Complementation Group G (FANCG))

    Alternative Name

    FANCG

    Background

    Target Description: The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity, they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group G.

    Gene Symbol: FANCG

    Molecular Weight

    68554 Da

    Gene ID

    2189

    UniProt

    O15287

    Pathways

    DNA Damage Repair
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