Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Damage Specific DNA Binding Protein 1 (DDB1) (Middle Region) Peptide

DDB1 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN5672220

Quick Overview for Damage Specific DNA Binding Protein 1 (DDB1) (Middle Region) Peptide (ABIN5672220)

Target

DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))

Origin

Human

Source

  • 4
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Sequence

    SIDLPGIKGL WPLRSDPNRE TDDTLVLSFV GQTRVLMLNG EEVEETELMG

    Characteristics

    This is a synthetic peptide designed for use in combination with anti- DDB1 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))

    Background

    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.

    Alias Symbols: XPE, DDBA, XAP1, XPCE, XPE-BF, UV-DDB1

    Protein Size: 1140

    Gene ID

    1642

    NCBI Accession

    NM_001923, NP_001914

    UniProt

    Q16531
You are here:
Chat with us!