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FANCD2 antibody

FANCD2 Reactivity: Human WB Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7267126
  • Target See all FANCD2 Antibodies
    FANCD2 (Fanconi Anemia, Complementation Group D2 (FANCD2))
    Reactivity
    • 67
    • 26
    • 23
    • 1
    • 1
    • 1
    Human
    Host
    • 66
    • 1
    Rabbit
    Clonality
    • 58
    • 9
    Monoclonal
    Conjugate
    • 27
    • 5
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FANCD2 antibody is un-conjugated
    Application
    • 23
    • 21
    • 15
    • 14
    • 14
    • 14
    • 8
    • 6
    • 5
    • 5
    • 4
    • 1
    • 1
    Western Blotting (WB)
    Purpose
    FANCD2 Rabbit mAb
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthesized peptide derived from human FANCD2.
    Isotype
    IgG
    Top Product
    Discover our top product FANCD2 Primary Antibody
  • 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
    FANCD2 (Fanconi Anemia, Complementation Group D2 (FANCD2))
    Alternative Name
    FANCD2 (FANCD2 Products)
    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 D2. This protein is monoubiquinated in response to DNA damage, resulting in its localization to nuclear foci with other proteins (BRCA1 AND BRCA2) involved in homology-directed DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016],FA4,FAD,FACD,FAD2,FA-D2,FANCD,FANCD2,Cell Biology & Developmental Biology,Cell Cycle,DNA Damage & Repair,Epigenetics & Nuclear Signaling,G2/M DNA Damage Checkpoint,FANCD2
    Molecular Weight
    166kDa
    Gene ID
    2177
    UniProt
    Q9BXW9
    Pathways
    DNA Damage Repair
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