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FANCI antibody

FANCI Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6569525
  • Target See all FANCI Antibodies
    FANCI (Fanconi Anemia Complementation Group I (FANCI))
    Reactivity
    • 14
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 13
    • 1
    Rabbit
    Clonality
    • 14
    Polyclonal
    Conjugate
    • 11
    • 1
    • 1
    • 1
    This FANCI antibody is un-conjugated
    Application
    • 9
    • 5
    • 3
    • 2
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human FANCI
    Isotype
    IgG
    Top Product
    Discover our top product FANCI Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    Buffer
    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
    FANCI (Fanconi Anemia Complementation Group I (FANCI))
    Alternative Name
    FANCI (FANCI Products)
    Synonyms
    KIAA1794 antibody, Fanconi anemia complementation group I antibody, Fanconi anemia, complementation group I antibody, FANCI antibody, Fanci antibody
    Background

    Synonyms: FANCI,FANCI gene,FANCI,Fanconi anemia group I protein,Fanconi anemia, complementation group I,FLJ10719,FLJ14658,KIAA1794,Protein FACI,Protein FANCI

    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 I. Alternative splicing results in two transcript variants encoding different isoforms.

    Molecular Weight

    Observed_MW: 170kDa

    Calculated_MW: 27kDa/142kDa/149kDa

    Gene ID
    55215
    UniProt
    Q9NVI1
    Pathways
    DNA Damage Repair
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