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 Specifications
    Catalog # Size Price
    XPA AntibodyReactivity: Human
    Applications: WB, IP, IHC-P, IF
    Immunogen: Between 1 and 50
    A301-780A100 µl (0.2 mg/ml) $339Add to Cart
    A301-780A-M100 µl (10 blots) $229Add to Cart
    A301-780A-T20 µl (2 blots) $50Add to Cart
    XPA IHC AntibodyApplications: IHC-P, IF
    Reactivity: Human, Mouse
    Immunogen: Between 1 and 50
    IHC-00344100 µl (50+ slides) $360Add to Cart
    IHC-00344-T10 µl (5+ slides) $50Add to Cart

    Please note that Cookies and JavaScript are required for you to view this website.

    Check if you have Cookies and JavaScript enabled in your browser