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XPC anticorps

XPC Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7254403
  • Antigène Voir toutes XPC Anticorps
    XPC (Xeroderma Pigmentosum, Complementation Group C (XPC))
    Reactivité
    • 47
    • 3
    • 3
    • 1
    Humain
    Hôte
    • 44
    • 7
    Lapin
    Clonalité
    • 45
    • 6
    Polyclonal
    Conjugué
    • 28
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp XPC est non-conjugé
    Application
    • 37
    • 26
    • 10
    • 7
    • 6
    • 6
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Synthetic peptide of human XPC
    Isotype
    IgG
    Top Product
    Discover our top product XPC Anticorps primaire
  • Indications d'application
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.66 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    XPC (Xeroderma Pigmentosum, Complementation Group C (XPC))
    Autre désignation
    XPC (XPC Produits)
    Synonymes
    anticorps RAD4, anticorps XP3, anticorps XPCC, anticorps XPC complex subunit, DNA damage recognition and repair factor, anticorps xeroderma pigmentosum, complementation group C, anticorps XPC, anticorps Xpc
    Sujet
    The protein encoded by this gene is a key component of the XPC complex, which plays an important role in the early steps of global genome nucleotide excision repair (NER). The encoded protein is important for damage sensing and DNA binding, and shows a preference for single-stranded DNA. Mutations in this gene or some other NER components can result in Xeroderma pigmentosum, a rare autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age. Alternatively spliced transcript variants have been found for this gene.
    UniProt
    Q01831
    Pathways
    Signalisation p53, Réparation de l'ADN
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