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WB analysis of multiple cells treated with 10-Gy IR using GTX25360 FANCD2 antibody [FI-17]. Dilution : 1:1000
WB analysis of multiple cells treated with 10-Gy IR using GTX25360 FANCD2 antibody [FI-17]. Dilution : 1:1000
WB analysis of multiple cells treated with 10-Gy IR using GTX25360 FANCD2 antibody [FI-17]. Dilution : 1:1000

FANCD2 antibody [FI-17]

GTX25360
GeneTex
ApplicationsImmunoPrecipitation, Western Blot, ChIP Chromatin ImmunoPrecipitation
Product group Antibodies
ReactivityHuman
TargetFANCD2
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Overview

  • Supplier
    GeneTex
  • Product Name
    FANCD2 antibody [FI-17] - Orthogonal Validated
  • Delivery Days Customer
    9
  • Antibody Specificity
    We do not recommend use of this product for Hamster,Mouse.
  • Application Supplier Note
    WB: 1:1000 - 1:2000. ChIP assay: 1:10 - 1:500. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoPrecipitation, Western Blot, ChIP Chromatin ImmunoPrecipitation
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    FI-17
  • Conjugate
    Unconjugated
  • Gene ID2177
  • Target name
    FANCD2
  • Target description
    FA complementation group D2
  • Target synonyms
    FA4; FACD; FAD; FAD2; FA-D2; FANCD; Fanconi anemia complementation group D2; Fanconi anemia group D2 protein
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDQ9BXW9
  • Protein Name
    Fanconi anemia group D2 protein
  • Scientific 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 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 two transcript variants encoding different isoforms. [provided by RefSeq]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203