Phospho-ATM/ATR Substrate Motif [(pS/pT) QG] MultiMab®Rabbit Monoclonal Antibody mix#6966,Cell Signaling Technology (CST),6966
Phospho-ATM/ATR Substrate Motif [(pS/pT) QG] MultiMab®Rabbit Monoclonal Antibody mix recognizes proteins containing phospho-Ser or phospho-Thr followed by Gln and Gly residues. To some extent, this antibody also recongizes proteins with an S*/T*Q motif.
Host
Rabbit
Reactivity
All Species Expected
Application
Western Blotting: 1:1000 Immunoprecipitation: 1:100
Platform ID
BAB119886778
Cell Signaling Technology (CST)
Contact
Tel: 877-616-2355,978-867-2388
Fax: 877-616-2355
Email:
Specifications
Scientific Background
Ataxia telangiectasia mutated kinase (ATM) and ataxia telangiectasia and Rad3-related kinase (ATR) are related kinases that regulate cell cycle checkpoints and DNA repair (1). The identified substrates for ATM are p53, p95/NBS1, MDM2, Chk2, BRCA1, CtIP, 4E-BP1, and Chk1 (1,2) The essential requirement for the substrates of ATM/ATR is S*/T*Q. Hydrophobic amino acids at positions -3 and -1, and negatively charged amino acids at position +1 are positive determinants for substrate recognition by these kinases. Positively charged residues surrounding the S*/T*Q are negative determinants for substrate phosphorylation (3). The complex phenotype of AT cells suggests that it likely has additional substrates (3). To better understand the kinase and identify substrates for ATM and the related kinase ATR, CST has developed antibodies that recognize phosphorylated serine or threonine in the S*/T*Q motif.Kastan, M.B. and Lim, D.S. (2000)Nature Rev. Mol. Cell Biol.1, 179-186.Zhao, H. and Piwnica-Worms, H. (2001)Mol. Cell. Biol.21, 4129-4139.Kim, S. T. et al. (1999)J. Biol. Chem.274, 37538-37543.
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