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FANCA antibody

The Rabbit Monoclonal anti-FANCA antibody has been validated for WB. It is suitable to detect FANCA in samples from Human.
Catalog No. ABIN7267124

Quick Overview for FANCA antibody (ABIN7267124)

Target

See all FANCA Antibodies
FANCA (Fanconi Anemia Group A Protein (FANCA))

Reactivity

  • 48
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  • 4
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  • 1
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Human

Host

  • 61
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Rabbit

Clonality

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Monoclonal

Conjugate

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  • 1
  • 1
  • 1
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This FANCA antibody is un-conjugated

Application

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Western Blotting (WB)
  • Purpose

    FANCA Rabbit mAb

    Cross-Reactivity

    Human

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human FANCA

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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

    FANCA (Fanconi Anemia Group A Protein (FANCA))

    Alternative Name

    FANCA

    Background

    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 A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq, Jul 2008],FA, FA-H, FA1, FAA, FACA, FAH, FANCH,DNA Damage & Repair,Epigenetics & Nuclear Signaling,FANCA

    Molecular Weight

    163Da

    Gene ID

    2175

    UniProt

    O15360

    Pathways

    DNA Damage Repair
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