NBS1 Antibody

Mutations in NBS1 (Nijmegen Breakage Syndrome 1), also known as nibrin, are associated with the autosomal recessive syndrome, Nijmegen breakage syndrome, characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. At the cellular level, NBS1 is part of the MRE11/RAD50 double-strand break repair complex that is critical to the DNA damage response, DNA recombination, telomere integrity, and cell cycle checkpoint control.
    Product/Catalog #SpecificationsPrice
    NBS1 Antibody
    A300-187A
    Reactivity: Human
    Applications: WB, IP
    $314.00
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    NBS1 Antibody
    A301-284A
    Reactivity: Mouse
    Applications: WB, IP
    $314.00
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    NBS1 Antibody
    A301-289A
    Reactivity: Human
    Applications: WB, IP, IHC-P, IF
    $314.00
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    NBS1 Antibody
    A301-290A
    Reactivity: Human
    Applications: WB, IP, IHC-P, IF, PLA
    $314.00
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    NBS1 Antibody AbVantageâ„¢ Pack
    A310-448A
    Applications: WB, IP, IHC-P, IF, PLA
    Reactivity: Human
    Quantity: 1 each of A300-187A, A301-284A, A301-289A, and A301-290A
    $868.00
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    NBS1 IHC Antibody
    IHC-00258
    Applications: IHC-P, IF
    Reactivity: Human
    Quantity: 0.1 ml (50 - 250 slides)
    $360.00
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