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The image on the left is immunohistochemistry of paraffin-embedded Human cervical cancer tissue using CSB-PA056628(DDB1 Antibody) at dilution 1/5, on the right is treated with synthetic peptide. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human cervical cancer tissue using CSB-PA056628(DDB1 Antibody) at dilution 1/5, on the right is treated with synthetic peptide. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human cervical cancer tissue using CSB-PA056628(DDB1 Antibody) at dilution 1/5, on the right is treated with synthetic peptide. (Original magnification: x200)

DDB1 Antibody

CSB-PA056628
Cusabio
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetDDB1
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Overview

  • Supplier
    Cusabio
  • Product Name
    DDB1 Antibody
  • Delivery Days Customer
    20
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID1642
  • Target name
    DDB1
  • Target description
    damage specific DNA binding protein 1
  • Target synonyms
    DDBA, UV-DDB1, WHIKERS, XAP1, XPCE, XPE, XPE-BF, DNA damage-binding protein 1, DDB p127 subunit, DNA damage-binding protein a, HBV X-associated protein 1, UV-DDB 1, UV-damaged DNA-binding factor, UV-damaged DNA-binding protein 1, XAP-1, XPE-binding factor, damage-specific DNA binding protein 1, 127kDa, xeroderma pigmentosum group E-complementing protein
  • Host
    Rabbit
  • 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.
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    41116161