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- 详细信息
- 文献和实验
- 技术资料
- 抗体英文名:
PTMScan Phospho-ATM/ATR Substrate (S*Q) Immunoaffinity Beads__®
- 供应商:
CST
- 级别:
详见MSDS文件
- 保质期:
详见说明书
- 库存:
大量
- 是否单克隆:
0
- 保存条件:
-20°c
| 规格: | 产品价格: | ¥请询价 | |
|---|---|---|---|
| 规格: | 产品价格: | ¥请询价 |
Product Pathways - Motif Antibodies
PTMScan® Phospho-ATM/ATR Substrate (S*Q) Immunoaffinity Beads #9884
| No. | Services Information | |
|---|---|---|
| 9884 | ptmscan@cellsignal.com |
| Consenus Site | Cell or Tissue Type | Study No. | Modified Peptides Identified |
|---|---|---|---|
| S*Q |
Services Information
This product is not for individual sale. It is only available as a component of the PTMScan® Proteomics System . PTMScan® Proteomics System orders must be priced out individually. Please email us at ptmscan@cellsignal.com to receive the most accurate pricing.
Description
PTMScan® Immunoaffinity Beads are custom preparations of motif antibodies coupled to protein A beads. They are intended only for use for PTMScan® and are available as components of the PTMScan® Proteomics System.
Specificity / Sensitivity
PTMScan® Phospho-ATM/ATR Substrate Motif (pS/pTQ) Immunoaffinity Beads detect and capture endogenous levels of peptide derived from protease digested cellular proteins containing phospho-Ser/Thr followed by Gln at the +1 position. The antibody does not cross-react with corresponding nonphosphorylated sequences or with other phospho-Ser/Thr-containing motifs. (U.S. Patent No's.: 6,441,140; 6,982,318; 7,259,022; 7,344,714; U.S.S.N. 11,484,485; and all foreign equivalents.)
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.
Application References
Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !
For Research Use Only. Not For Use In Diagnostic Procedures.
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文献和实验obtained with use of cells synchronized such way as representing unperturbed cells. The protocol presented in this chapter describes the methodology of assessment of phosphorylation of histone H2AX-Ser 139, ATM/ATR substrate on Ser/Thr at SQ/TQ cluster
acquiring the instrumentation required for real-time analysis, this technique is becoming the dominant RT-PCR-based quantitation technique. Real-Time PCR Chemistries Currently four different chemistries, TaqMan® (Applied Biosystems, Foster City, CA, USA
Genome‐Wide Location Analysis by Pull Down of In Vivo Biotinylated Transcription Factors
, H., McPhillips, T., Xu, X., Cao, A.R., Iyengar, S., Nicolet, C.M., Ludascher, B., Korf, I., and Farnham, P.J. 2010. Sole‐Search: An integrated analysis program for peak detection and functional annotation using ChIP‐seq data. Nucleic Acids Res. 38
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