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Damage-Specific DNA Binding Protein 2, 48kDa (DDB2) Peptide

DDB2 Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN939596
  • Target See all DDB2 products
    DDB2 (Damage-Specific DNA Binding Protein 2, 48kDa (DDB2))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 2
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    IVVGRYPDPN FKSCTPYELR TIDVFDGNSG KMMCQLYDPE SSGISSLNEF
    Characteristics
    A synthetic peptide for use as a blocking control in assays to test for specificity of DDB2 antibody,
    Alternative Names: DDB2 control peptide, DDB2 antibody Blocking Peptide, Anti-DDB2 Blocking Peptide, damage-specific DNA binding protein 2, 48kDa Blocking Peptide, DDBB Blocking Peptide, FLJ34321 Blocking Peptide, UV-DDB2 Blocking Peptide, DDB2, DDB-2, DDB 2, DDB-2 Blocking Peptide, DDB 2 Blocking Peptide
  • Application Notes
    Optimal conditions should be determined by the investigator
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20 °C long term.
  • Target
    DDB2 (Damage-Specific DNA Binding Protein 2, 48kDa (DDB2))
    Background
    This gene encodes a protein that is necessary for the repair of ultraviolet light-damaged DNA. This protein is the smaller subunit of a heterodimeric protein complex that participates in nucleotide excision repair, and this complex mediates the ubiquitylation of histones H3 and H4, which facilitates the cellular response to DNA damage. This subunit appears to be required for DNA binding. Mutations in this gene cause xeroderma pigmentosum complementation group E, a recessive disease that is characterized by an increased sensitivity to UV light and a high predisposition for skin cancer development, in some cases accompanied by neurological abnormalities.
    Molecular Weight
    48 kDa
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