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

DDB1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN8098512
168,15 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour Damage Specific DNA Binding Protein 1 (DDB1) (Middle Region) Peptide (ABIN8098512)

Antigène

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

Origine

Humain

Source

  • 7
Synthetic

Application

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

    Middle Region

    Fonction

    DDB1 Peptide - middle region

    Séquence

    IGIHEHASID LPGIKGLWPL RSDPNRETDD TLVLSFVGQT RVLMLNGEEV
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Commentaires

    This is a synthetic peptide designed for use in combination with anti-DDB1 Antibody (ARP73816_P050),. 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. Please inquire for more details.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Buffer

    Lyophilized powder

    Stock

    -20 °C

    Stockage commentaire

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

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

    Sujet

    Background Information: 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.

    Alternative Symbols: DDB1,XAP1,

    Poids moléculaire

    125kDa

    ID gène

    1642

    NCBI Accession

    XP_005273861

    UniProt

    Q16531
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