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  • Anti Atm F858l Mouse Monoclonal Antibody - USA

    price: contact company for price

    Catalog Number: 26141

    Gene Symbol: ATM

    Description: Anti-ATM (F858L) Mouse Monoclonal Antibody

    Background: Ataxia telangiectasia mutated (ATM) is a serine/threonine protein kinase that is recruited and activated by DNA double-strand breaks. It phosphorylates several key proteins that initiate activation of the DNA damage checkpoint, leading to cell cycle arrest, DNA repair or apoptosis. Activity of ATM protein is under tight control, and mutation of ATM can cause disease such as Ataxia telangiectasia (AT) and cancers.

    Immunogen: A synthetic peptide from the internal region of ATM which includes the mutation of F858L, human origin.

    Applications: ELISA, WB, IHC

    Recommended Dilutions:

    ELISA: 1:1000-1:5000

    WB: 1:100-1:1000

    IHC: 1:50-1:100

    Concentration: 1 mg/ml

    Host: Mouse

    Format: Liquid

    Clonality: Monoclonal

    Isotype:

    Purity: Purified from ascites

    Storage buffer:

    Preservative: no

    Constituents: PBS (without Mg2+ and Ca2+), pH 7.4, 150 mM NaCl, 50% glycerol

    Species Reactivity: Recognizes ATM (F858L), but not wild type ATM protein from vertebrates.

    Storage Conditions: Store at -20°C. Avoid freeze / thaw cycles


    Company Contact:


    • Phone: 6109452007

    • Address: 24 Whitewoods Lane, Malvern, PA, USA

    • Email: Email


    Published date: June 6, 2013 -

    • Business Description: NewEast Biosciences are specialized in generating protein configuration specific monoclonal antibodies that recognize active (GTP bound) G proteins (including Ras superfamily small GTPases and heterotrimeric G proteins). These unique antibodies do not recognize the inactive (GDP bound) G proteins. These monoclonal antibodies have been successfully used to immunoprecipitate active G proteins from cell lysates, and for immunohistochemical staining of active G proteins in cultured cells or in tissue sections. Hence, these antibodies can be used to study the spatial and temporal dynamics of cellular signaling involving big and small G proteins, the future direction of signal transduction studies.

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