Anti-Human ATM (Clone FHC-116) – Purified No Carrier Protein

Anti-Human ATM (Clone FHC-116) – Purified No Carrier Protein

Product No.: LTCC234

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Clone
FHC-116
Target
ATM
Formats AvailableView All
Product Type
Recombinant 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 Details

Product Details

Reactive Species
Human
Host Species
HEK-293
Immunogen
ATM synthetic peptide SLEIS[+80]QSYTTTQR
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.

Description

Description

Specificity
FHC-116-38-6 activity is directed against human ATM peptide sequence SLEISQSYTTTQR.
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-116-38-6 was generated in rabbit for use in immuno-MRM assays using a synthetic peptide derived from residues 363-375 of human ATM that was phosphorylated at S367, SLEIS[ph]QSYTTTQR2,3,4. https://antibodies.cancer.gov/detail/CPTC-ATM-2#CPTC-ATM-2
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
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Tumor Suppressors
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DNA Damage
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Neurodegeneration

References & Citations

1 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-3211

Formats Available

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Disclaimer AlertProducts are for research use only. Not for use in diagnostic or therapeutic procedures.