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DDB2 anticorps

DDB2 Reactivité: Humain, Souris, Rat WB, IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7009799
  • Antigène Voir toutes DDB2 Anticorps
    DDB2 (Damage-Specific DNA Binding Protein 2, 48kDa (DDB2))
    Reactivité
    • 37
    • 16
    • 12
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 36
    • 3
    Lapin
    Clonalité
    • 27
    • 12
    Polyclonal
    Conjugué
    • 21
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Cet anticorp DDB2 est non-conjugé
    Application
    • 21
    • 9
    • 5
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human DDB2 (NP_000098.1).
    Isotype
    IgG
    Top Product
    Discover our top product DDB2 Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000 IF 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    DDB2 (Damage-Specific DNA Binding Protein 2, 48kDa (DDB2))
    Autre désignation
    DDB2 (DDB2 Produits)
    Synonymes
    anticorps 2610043A19Rik, anticorps si:dkey-45f10.3, anticorps DDBB, anticorps UV-DDB2, anticorps damage specific DNA binding protein 2, anticorps damage-specific DNA binding protein 2, anticorps DDB2, anticorps ddb2, anticorps Ddb2
    Sujet
    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. Two transcript variants encoding different isoforms have been found for this gene.
    Poids moléculaire

    Observed_MW: 48 kDa

    Calculated_MW: 17 kDa/26 kDa/40 kDa/47 kDa

    ID gène
    1643
    UniProt
    Q92466
    Pathways
    Réparation de l'ADN
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