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WB analysis of NIH-3T3 (A) and NS0 (B) lysate. using GTX89975 DDB1 antibody, C-term. Dilution : 0.01microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of NIH-3T3 (A) and NS0 (B) lysate. using GTX89975 DDB1 antibody, C-term. Dilution : 0.01microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of NIH-3T3 (A) and NS0 (B) lysate. using GTX89975 DDB1 antibody, C-term. Dilution : 0.01microg/ml Loading : 35microg protein in RIPA buffer

DDB1 antibody, C-term

GTX89975
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman, Mouse
TargetDDB1
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Overview

  • Supplier
    GeneTex
  • Product Name
    DDB1 antibody, C-term
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 1-2microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID1642
  • Target name
    DDB1
  • Target description
    damage specific DNA binding protein 1
  • Target synonyms
    damage-specific DNA binding protein 1, 127kDa; DDB p127 subunit; DDBA; DNA damage-binding protein 1; DNA damage-binding protein a; HBV X-associated protein 1; UV-damaged DNA-binding factor; UV-damaged DNA-binding protein 1; UV-DDB 1; UV-DDB1; WHIKERS; XAP1; XAP-1; xeroderma pigmentosum group E-complementing protein; XPCE; XPE; XPE-BF; XPE-binding factor
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ16531
  • Protein Name
    DNA damage-binding protein 1
  • Scientific Description
    The protein encoded by this gene is the large subunit (p127) of the heterodimeric DNA damage-binding (DDB) complex while another protein (p48) forms the small subunit. This protein complex functions in nucleotide-excision repair and binds to DNA following UV damage. Defective activity of this complex causes the repair defect in patients with xeroderma pigmentosum complementation group E (XPE) - an autosomal recessive disorder characterized by photosensitivity and early onset of carcinomas. However, it remains for mutation analysis to demonstrate whether the defect in XPE patients is in this gene or the gene encoding the small subunit. In addition, Best vitelliform mascular dystrophy is mapped to the same region as this gene on 11q, but no sequence alternations of this gene are demonstrated in Best disease patients. The protein encoded by this gene also functions as an adaptor molecule for the cullin 4 (CUL4) ubiquitin E3 ligase complex by facilitating the binding of substrates to this complex and the ubiquitination of proteins. [provided by RefSeq, May 2012]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203