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FANCF antibody

FANCF Reactivity: Human ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7236947
  • Target See all FANCF Antibodies
    FANCF (Fanconi Anemia, Complementation Group F (FANCF))
    Reactivity
    • 17
    • 2
    • 1
    Human
    Host
    • 14
    • 2
    • 2
    Rabbit
    Clonality
    • 17
    • 1
    Polyclonal
    Conjugate
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FANCF antibody is un-conjugated
    Application
    • 10
    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human FANCF
    Isotype
    IgG
    Top Product
    Discover our top product FANCF Primary Antibody
  • Application Notes
    IHC 1:100-1:300
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.8 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    FANCF (Fanconi Anemia, Complementation Group F (FANCF))
    Alternative Name
    FANCF (FANCF Products)
    Synonyms
    FAF antibody, A730016A17 antibody, RGD1561456 antibody, Fanconi anemia complementation group F L homeolog antibody, Fanconi anemia, complementation group F antibody, Fanconi anemia complementation group F antibody, fancf.L antibody, fancf antibody, FANCF antibody, Fancf antibody
    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 F.
    NCBI Accession
    NP_073562
    UniProt
    Q9NPI8
    Pathways
    DNA Damage Repair
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