PTMScan   Phospho-Thr-X-Arg Motif (T*XR) Immunoaffinity Beads__®

PTMScan Phospho-Thr-X-Arg Mo

tif (T*XR) Immunoaffinity Beads__®
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  • 询价
  • Cell Signaling Technology已认证
  • 1988
  • USA
  • 2025年10月05日
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    • 详细信息
    • 技术资料
    • 抗体英文名

      PTMScan Phospho-Thr-X-Arg Motif (T*XR) Immunoaffinity Beads__®

    • 级别

      详见MSDS文件

    • 供应商

      CST

    • 库存

      大量

    • 保质期

      详见说明书

    • 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-Thr-X-Arg Motif (T*XR) Immunoaffinity Beads #1988

    No.   Services Information
    1988 In Stock ptmscan@cellsignal.com
    Consenus Site Cell or Tissue Type Study No. Modified Peptides Identified
    T*X(K/R) HeLa (human epithelial carcinoma) 2655 82 PDF XLS

    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-Thr-X-Arg Motif (T*XR) Immunoaffinity Beads detect and capture endogenous levels of peptide derived from protease digested cellular proteins containing the phospho-Thr-X-Arg motif. Pro is preferred but not necessary at +1 position. (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.)

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa cells, untreated or nocodazole-treated, using Phospho-Threonine-X-Arginine Antibody, the unconjugated antibody corresponding to PTMScan® Phospho-Thr-X-Arg Motif (T*XR) Immunoaffinity Beads.

    Background

    Some signaling molecules can be regulated by phosphorylation at a specific threonine followed by arginine or lysine at the +2 position. For example, conventional PKC isozymes phosphorylate substrates containing serine or threonine with Arg or Lys at the -3, -2 and +2 positions (1-2). c-Raf, a mitogen-activated protein kinase and the main effector recruited by GTP-bound Ras, is phosphorylated at Thr481 and Thr491 followed by Lys at the +2 position (3). Phosphorylation of these sites is important for enzyme activities. To determine the phosphorylation state of Thr in the Thr-X-Arg motif, and to identify potential new phosphorylation sites with this motif, Cell Signaling Technology has developed a Phospho-Threonine X-Arginine Antibody that recognizes phosphorylated Thr followed by Arg or Lys at the +2 position.

    1. Nishikawa, K. et al. (1997) J Biol Chem 272, 952-60.
    2. Pearson, R.B. and Kemp, B.E. (1991) Methods Enzymol 200, 62-81.
    3. Zhang, B.H. and Guan, K.L. (2000) EMBO J 19, 5429-39.

    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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