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

DDB2 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN8098515
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 2, 48kDa (DDB2) (C-Term) Peptide (ABIN8098515)

Antigène

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

Origine

Humain

Source

  • 4
Synthetic

Application

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

    C-Term

    Fonction

    DDB2 Peptide - C-terminal region

    Séquence

    IVVGRYPDPN FKSCTPYELR TIDVFDGNSG KMMCQLYDPE SSGISSLNEF
  • 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-DDB2 Antibody (ARP60163_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

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

    Sujet

    Background Information: 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.

    Alternative Symbols: DDBB, FLJ34321, UV-DDB2

    Poids moléculaire

    48kDa

    ID gène

    1643

    NCBI Accession

    NP_000098

    UniProt

    Q92466
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