XPA Antibody

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.
    Product/Catalog #SpecificationsPrice
    XPA Antibody
    A301-780A
    Reactivity: Human
    Applications: WB, IP, IHC-P, IF
    $314.00
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    XPA IHC Antibody
    IHC-00344
    Applications: IHC-P, IF
    Reactivity: Human, Mouse
    Quantity: 0.1 ml (50 - 250 slides)
    $360.00
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