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XPA anticorps (AA 1-50)

XPA Reactivité: Humain WB, IP, IHC (fp) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7454782
  • Antigène Voir toutes XPA Anticorps
    XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))
    Épitope
    • 13
    • 8
    • 8
    • 7
    • 5
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-50
    Reactivité
    • 60
    • 24
    • 11
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 54
    • 6
    Lapin
    Clonalité
    • 56
    • 4
    Polyclonal
    Conjugué
    • 31
    • 5
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp XPA est non-conjugé
    Application
    • 43
    • 25
    • 10
    • 8
    • 8
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
    Fonction
    Rabbit anti-XPA Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogène
    Between AA 1 and 50
    Isotype
    IgG
    Top Product
    Discover our top product XPA Anticorps primaire
  • Indications d'application

    IHC: 1:200 to 1:1000. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions
    For Research Use only
  • Concentration
    200 μg/mL
    Buffer
    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide
    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
    4 °C
    Date de péremption
    12 months
  • Antigène
    XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))
    Autre désignation
    XPA (XPA Produits)
    Synonymes
    anticorps CG6358, anticorps DhR14, anticorps DhXPA, anticorps DmXPA, anticorps Dmel\\CG6358, anticorps Dxpa, anticorps EG:EG0007.8, anticorps XPAC, anticorps XPA_DROME, anticorps Xpa, anticorps dmXPA, anticorps dxpa, anticorps XP1, anticorps AI573865, anticorps Xpac, anticorps xpac, anticorps xxpa, anticorps Xeroderma pigmentosum group A-like, anticorps XPA, DNA damage recognition and repair factor, anticorps xeroderma pigmentosum, complementation group A, anticorps xeroderma pigmentosum, complementation group A L homeolog, anticorps Xpac, anticorps XPA, anticorps Xpa, anticorps xpa.L
    Sujet
    Background: Mutations in XPA (xeroderma pigmentosum group A-complementing protein) are the cause of xeroderma pigmentosum A (XP-A), an autosomal recessive disease that is mainly characterized by a susceptibility to UV-induced skin cancer and in some cases neurological abnormalities. XPA is one of seven XP complementation groups that have been identified. The XP complementation groups represent genes critical to the nucleotide excision repair (NER) pathway. XPA is thought to function in the recognition of DNA damage and as a processivity factor for XPF and XPG.
    ID gène
    7507
    NCBI Accession
    NP_000371
    UniProt
    P23025
    Pathways
    Réparation de l'ADN
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