Phospho-Threonine (42H4) Mouse mAb产品图

Phospho-Threonine (42H4) Mouse

mAb
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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2026年05月28日
  • W, IP, E-P
  • All
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名:

      Phospho-Threonine (42H4) Mouse mAb

    • 抗原:

      phospho-Thr-containing peptides

    • 应用范围:

      W, IP, E-P

    • 供应商:

      CST

    • 适应物种:

      All

    • 保质期:

      详见说明书

    • 库存:

      大量

    • 级别:

      详见MSDS文件

    • 是否单克隆:

      1

    • 保存条件:

      -20°c

    • 规格:

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting  IP=Immunoprecipitation  E-P=ELISA (Peptide)
    Reactivity Key: All=All species expected
    Species cross-reactivity is determined by western blot.

    Applications Reactivity Sensitivity Isotype
    W IP E-P All Endogenous Mouse IgM
    Protocols
    Specificity / Sensitivity

    Phospho-Threonine (42H4) Mouse mAb binds phosphorylated threonine residues in a manner largely independent of the surrounding amino acid sequence. The antibody is phospho-specific but does not cross-react with phospho-tyrosine-containing sequences. It does show slight cross-reactivity with a few phospho-serine-containing peptides. By ELISA, it recognizes a wide variety of threonine-phosphorylated peptides. (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.)

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with phospho-Thr-containing peptides.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from A431 cells, untreated or treated with calyculin A, a threonine phosphatase inhibitor, or extracts from NIH/3T3 cells, untreated or treated with pervanadate, a tyrosine phosphatase inhibitor, using Phospho-Threonine (42H4) Mouse mAb (upper) or Phospho-Tyrosine Monoclonal Antibody (P-Tyr-100) #9411 (lower).

    ELISA-Peptide

    ELISA-Peptide

    Phospho-Threonine (42H4) Mouse mAb ELISA Assay: Signal-to-noise ratio of phospho- versus nonphospho-peptides. (T* denotes phosphorylated threonine.)

    Background

    Much of the dynamic behavior of cellular proteins, including the regulation of molecular interactions (1), subcellular localization (2), and transcriptional regulation (3) is controlled by a variety of post-translational modifications (4). Antibodies specific for these post-translational modifications are invaluable tools in the quest to understand normal and pathogenic molecular and cellular behavior.General protein modification antibodies are designed to react with modified amino acid residues (e.g. phospho-threonine, phospho-tyrosine, acetyl-lysine, nitro-tyrosine) independently of the sequence in which they are embedded. This ability to recognize modified residues in a "context-independent" fashion gives these antibodies broad reactivities, presumably conferring upon them the ability to react with hundreds of distinct proteins. This broad pattern of reactivity makes these antibodies especially valuable in multiplex analyses and target discovery programs.

    Protein kinases are among the most abundant eukaryotic regulatory proteins; over 500 separate kinase genes are encoded in mammalian genomes (5,6). In spite of the importance of kinases in eukaryotic biology, relatively few of their physiological targets are known. Phospho-Threonine Antibody (P-Thr-Polyclonal) #9381 and Phospho-Threonine (42H4) Monoclonal Antibody #9386 provide powerful tools for discovering targets of serine/threonine kinases, for monitoring and characterizing in vitro threonine phosphorylation reactions as well as for high throughput Ser/Thr kinase drug discovery.

    1. Yaffe, M.B. and Elia, A.E. (2001) Curr Opin Cell Biol 13, 131-8.
    2. Appella, E. and Anderson, C.W. (2001) Eur J Biochem 268, 2764-72.
    3. Jenuwein, T. and Allis, C.D. (2001) Science 293, 1074-80.
    4. Krishna, R.G. and Wold, F. (1993) Adv Enzymol Relat Areas Mol Biol 67, 265-98.
    5. Venter, J.C. et al. (2001) Science 291, 1304-51.
    6. Manning, G. et al. (2002) Science 298, 1912-34.
    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 !

    Companion Products

    License/Use Restrictions: Use of CST Motif Antibodies within certain methods (e.g., U.S. Patent No.'s 7,198,896 & 7,300,753) may require a license from CST. For information regarding academic licensing terms please have your technology transfer office contact CST Legal Department at CST_ip@cellsignal.com. For information regarding commercial licensing terms please contact CST Pharma Services Department at ptmscan@cellsignal.com.


    For Research Use Only. Not For Use In Diagnostic Procedures.

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    图标文献和实验
    相关实验
    • Purification of mAb (IgG)

      (adjust pH to 7.8 with Binding buffer; red color) to the Protein A column.Mouse antibodies of the IgG1 subclass do not have a high affinity for protein A. Purification on protein A beads using standard conditions will yield approximately 1/10

    • 【求助】抗体制备服务

      -phosphoserine的抗体。 摘抄: Anti-Phosphothreonine (MAb) - CryptateThe anti-phosphothreonine antibody is a monoclonal antibody (clone 42H4) produced at Cell Signaling Technology (reference 9386). It recognizes phosphorylated threonine residues in a manner

    • CD42a/CD42b/CD42c/CD42d分子

      staining (normal): platelets and megakaryocytes   CD42d Aka platelet GP V CD42d mouse monoclonal antibodies are used to detect auto- and allo-anti-platelet antibodies Co-expression studies suggest that CD42d may be essential

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