Phospho-Tyrosine Mouse mAb (P-Tyr-102)产品图

Phospho-Tyrosine Mouse mAb (P-

Tyr-102)
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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2026年10月11日
  • W, IP, IHC-P, F, 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-Tyrosine Mouse mAb (P-Tyr-102)

    • 抗原:

      synthetic phospho-Tyr-containing peptides

    • 应用范围:

      W, IP, IHC-P, F, E-P

    • 级别:

      详见MSDS文件

    • 供应商:

      CST

    • 保质期:

      详见说明书

    • 适应物种:

      All

    • 库存:

      大量

    • 是否单克隆:

      1

    • 保存条件:

      -20°c

    • 规格:

      100 ug (40 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ug (40 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  IHC-P=Immunohistochemistry (Paraffin)  F=Flow Cytometry  E-P=ELISA (Peptide)
    Reactivity Key: All=All species expected
    Species cross-reactivity is determined by western blot.

    Applications Reactivity Sensitivity Isotype
    W IP IHC-P F E-P All Endogenous Mouse IgG1
    Protocols
    Specificity / Sensitivity

    Phospho-Tyrosine Mouse mAb (P-Tyr-102) is a high affinity IgG1 monoclonal antibody. ELISAs using a wide variety of phospho-peptides show that P-Tyr-102 binds phospho-Tyr in a manner largely independent of the surrounding amino acid sequence.2D gel western blot analysis of pervanadate-treated cell extracts also shows that P-Tyr-102 interacts with a broad range of tyrosine-phosphorylated proteins. P-Tyr-102's fine specificity in terms of the sequence context in which it can recognize phospho-tyrosine seems to differ slightly from that of P-Tyr-100 #9411. P-Tyr-102 does not recognize peptides containing phospho-Ser or phospho-Thr. (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 synthetic phospho-Tyr-containing peptides .

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from sodium vanadate treated (3 mM for 0.5 hour) NIH/3T3 cells, using Phospho-Tyrosine Mouse mAb (P-Tyr-102).

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from Jurkat cells treated with 1 mM pervanadate for 30 minutes prior to lysis. Proteins were separated by 2D electrophoresis prior to blotting.

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded human breast carcinoma, using Phospho-Tyrosine Mouse mAb (P-Tyr-102).


    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded NCI-H1650 xenograft untreated (left) or lambda-phosphatase-treated (right), using Phospho-Tyrosine Mouse mAb (P-Tyr-102).

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of NIH/3T3 cells, untreated (blue) or pervanadate-treated (green), using Phospho-Tyrosine Mouse mAb (P-Tyr-102) compared with a nonspecific negative control antibody (red).

    ELISA-Peptide

    ELISA-Peptide

    Phospho-Tyrosine Mouse mAb (P-Tyr-102) ELISA Assay: Signal-to-noise ratio of phospho- versus nonphospho-peptides. (Y* denotes phosphorylated tyrosine.)


    Background

    Tyrosine phosphorylation plays a key role in cellular signaling (1). In cancer, unregulated tyrosine kinase activity can drive malignancy and tumor formation by generating inappropriate proliferation and survival signals (2). Antibodies specific for phospho-tyrosine (3,4) have been invaluable reagents in these studies. The phospho-tyrosine monoclonal antibodies developed by Cell Signaling Technology provide exceptionally sensitive new tools of increased utility for studying tyrosine phosphorylation and monitoring tyrosine kinase activity in high throughput drug discovery.

    1. Schlessinger, J. (2000) Cell 103, 211-25.
    2. Blume-Jensen, P. and Hunter, T. (2001) Nature 411, 355-65.
    3. Ward, S.G. et al. (1992) J Biol Chem 267, 23862-9.
    4. Glenney, J.R. et al. (1988) J Immunol Methods 109, 277-85.
    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

    • T-Cell Activation Using mAb to CD3

      of specific protein tyrosine kinases (PTKs), breakdown of phosphatidylinositol 4,5-biphosphate (PIP2), activation of protein kinase C (PKC) and elevation of intracellular calcium ion concentration. These early events are transmitted to the nucleus and result

    • Purification of mAb (IgG)

        Purification of mAb (IgG) by Chang-Duk Jun, 03/14/2000 Purpose Materials Antibody 7E3 , 2L sup grown in flasks, frozen and thawed overnight. BioRad Affi-Gel Protein A MAPS II Buffers

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