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WB analysis of HeLa cell lysate using GTX30142 FANCD2 antibody.
WB analysis of HeLa cell lysate using GTX30142 FANCD2 antibody.
WB analysis of HeLa cell lysate using GTX30142 FANCD2 antibody.

FANCD2 antibody

GTX30142
GeneTex
ApplicationsFlow Cytometry, ImmunoPrecipitation, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityCanine, Human, Mouse, Primate
TargetFANCD2
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Overview

  • Supplier
    GeneTex
  • Product Name
    FANCD2 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:10000 - 1:20000. IHC-P: 2.5 - 5 microg/ml. IP: 1:10 - 1:500. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Flow Cytometry, ImmunoPrecipitation, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID2177
  • Target name
    FANCD2
  • Target description
    FA complementation group D2
  • Target synonyms
    FA-D2, FA4, FACD, FAD, FAD2, FANCD, Fanconi anemia group D2 protein, Fanconi anemia complementation group D2
  • Host
    Rabbit
  • Isotype
    IgG
  • 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
    Canine, Human, Mouse, Primate
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Oberholster L, Mathias A, Perriot S, et al. Comprehensive proteomic analysis of JC polyomavirus-infected human astrocytes and their extracellular vesicles. Microbiol Spectr. 2023,11(6):e0275123. doi: 10.1128/spectrum.02751-23
    Read this paper
  • Niraj J, Caron MC, Drapeau K, et al. The identification of FANCD2 DNA binding domains reveals nuclear localization sequences. Nucleic Acids Res. 2017,45(14):8341-8357. doi: 10.1093/nar/gkx543
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  • Huehls AM, Huntoon CJ, Joshi PM, et al. Genomically Incorporated 5-Fluorouracil that Escapes UNG-Initiated Base Excision Repair Blocks DNA Replication and Activates Homologous Recombination. Mol Pharmacol. 2016,89(1):53-62. doi: 10.1124/mol.115.100164
    Read this paper
  • Truong LN, Li Y, Sun E, et al. Homologous recombination is a primary pathway to repair DNA double-strand breaks generated during DNA rereplication. J Biol Chem. 2014,289(42):28910-23. doi: 10.1074/jbc.M114.576488
    Read this paper
  • Castillo A, Paul A, Sun B, et al. The BRCA1-interacting protein Abraxas is required for genomic stability and tumor suppression. Cell Rep. 2014,8(3):807-17. doi: 10.1016/j.celrep.2014.06.050
    Read this paper
  • Liu R, Hu T, Li JH, et al. Diagnosis of Fanconi anemia in children with atypical clinical features: a primary study. Chin Med J (Engl). 2013,126(23):4483-6.
    Read this paper
  • Geng L, Huntoon CJ, Karnitz LM. RAD18-mediated ubiquitination of PCNA activates the Fanconi anemia DNA repair network. J Cell Biol. 2010,191(2):249-57. doi: 10.1083/jcb.201005101
    Read this paper
  • Boichuk S, Hu L, Hein J, et al. Multiple DNA damage signaling and repair pathways deregulated by simian virus 40 large T antigen. J Virol. 2010,84(16):8007-20. doi: 10.1128/JVI.00334-10
    Read this paper
  • Hicks JK, Chute CL, Paulsen MT, et al. Differential roles for DNA polymerases eta, zeta, and REV1 in lesion bypass of intrastrand versus interstrand DNA cross-links. Mol Cell Biol. 2010,30(5):1217-30. doi: 10.1128/MCB.00993-09
    Read this paper
  • Wagner JM, Karnitz LM. Cisplatin-induced DNA damage activates replication checkpoint signaling components that differentially affect tumor cell survival. Mol Pharmacol. 2009,76(1):208-14. doi: 10.1124/mol.109.055178
    Read this paper