Anti-Human ATM [Clone CPTC-ATM-4] – Purified No Carrier Protein
Anti-Human ATM [Clone CPTC-ATM-4] – Purified No Carrier Protein
Product No.: LTCC233
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Clone FHC-114 Target ATM Formats AvailableView All Product Type Hybridoma Monoclonal Antibody Alternate Names Serine-protein kinase ATM, EC:2.7.11.1, Ataxia telangiectasia mutated (A-T mutated) Isotype Rabbit IgG Applications immuno-MRM |
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Antibody DetailsProduct DetailsReactive Species Human Host Species HEK-293 Immunogen ATM synthetic peptide phospho NLS[+80]DIDQSFNK Product Concentration ≥1.0 mg/ml Purity ≥90% monomer by analytical SEC Formulation This monoclonal antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 - 7.4 with no carrier protein, potassium, calcium or preservatives added. State of Matter Liquid Product Preparation Purified antibodies are manufactured in an animal free facility using only in vitro protein free cell culture techniques and are purified by a multi-step process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates. Storage and Handling This antibody may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at ≤ -70°C. Avoid Repeated Freeze Thaw Cycles. Regulatory Status Research Use Only Country of Origin USA Shipping 2 – 8° C Wet Ice Additional Applications Reported In Literature ? Immuno-MRM Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change. DescriptionDescriptionSpecificity FHC-114-18-2 activity is directed against human ATM peptide sequence
NLSDIDQSFNK. CPTC Clone ID CPTC-ATM-4 Background ATM is a phosphoinositide 3-kinase-related kinase1 that functions in the DNA damage response
(DDR) pathway by mediating a large phosphosignaling network in conjunction with ATR
kinases2. ATM is canonically activated by double-strand DNA breaks1. Phosphosignaling is then
used to modulate protein activity and interactions of ATM substrates and to affect their sub-
cellular localization2. Several hundred ATM substrates have been identified, many of which are
involved in DNA repair, cell cycle checkpoints, and/or apoptosis1. ATM kinase activity is
usually specific to serine or threonine residues, and less commonly glutamine. Oxidative stress
can also induce ATM activity and is used to modulate mitochondrial homeostasis. ATM dysregulation leads to radiation sensitivity, increases the risk of cancer, and is associated with neurological and immunological disorders2. Additionally, nonsense or missense mutations in the ATM gene cause ataxia telangiectasia, a rare autosomal recessive disorder that causes cerebellar degeneration, ataxia, immunodeficiency, thymic and gonadal atrophy, radiation sensitivity, and a predisposition to cancer1. FHC-114-18-2 was generated in rabbit for use in immuno-MRM assays using a synthetic peptide derived from residues 2994-3004 of human ATM that was phosphorylated at S2996, NLS[ph]DIDQSFNK2,3,4. https://antibodies.cancer.gov/detail/CPTC-ATM-4#CPTC-ATM-4 Antigen Distribution ATM is widely expressed and primarily located in the nucleus but is also
found in endocytic vesicles in association with beta-adaptin and can be translocated to
peroxisomes in response to reactive oxygen species. Ligand/Receptor p53/TP53, ABL1, BRCA1, TERF1, MRN complex NCBI Gene Bank ID UniProt.org Research Area Immuno-Oncology . Tumor Suppressors . DNA Damage . Neurodegeneration References & Citations1 Lee JH, Paull TT. Nat Rev Mol Cell Biol. 22(12):796-814. 2021. 2 Whiteaker JR, Zhao L, Saul R, et al. Radiat Res. 189(5):505-518. 2018. 3 Whiteaker JR, Lundeen RA, Zhao L, et al. Front Immunol. 12:765898. 2021. 4 https://assays.cancer.gov/CPTAC-5979 |
Formats Available
Products are for research use only. Not for use in diagnostic or therapeutic procedures.
