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Phospho-p56Dok-2 (Tyr351) Anti

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月30日
  • W
  • Rabbit
  • H,M
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-p56Dok-2 (Tyr351) Antibody

    • 抗原

      synthetic phosphopeptide corresponding to residues surrounding Tyr351 of mouse p56Dok-2

    • 应用范围

      W

    • 宿主

      Rabbit

    • 级别

      详见MSDS文件

    • 适应物种

      H,M

    • 库存

      大量

    • 供应商

      CST

    • 保质期

      详见说明书

    • 是否单克隆

      2

    • 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

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting
    Reactivity Key:  H=Human  M=Mouse
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Source
    W H (M) Transfected Only 56 to 58 Rabbit
    Protocols
    Specificity / Sensitivity

    Phospho-p56Dok-2 (Tyr351) Antibody detects transfected levels of p56Dok-2 only when phosphorylated at tyrosine 351. The antibody does not cross-react with other tyrosine phosphorylated p62Dok family members.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Tyr351 of mouse p56Dok-2. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from Jurkat cells transfected with p56Dok-2 proteins, untreated or stimulated with anti-CD2 antibody, using Phospho-p56Dok-2 (Tyr351) Antibody (upper) or p56Dok-2 Antibody #3914 (lower).

    Background

    Docking proteins are substrates of tyrosine kinases that function in the recruitment and assembly of specific signal transduction molecules. There are five members in the p62dok family, p62Dok (Dok-1), p56Dok-2 (Dok-2, or DoK-R), Dok-3, Dok-4 and Dok-5 (1-3), characterized by the presence of an amino-terminal PH domain, a central PTB domain and numerous potential sites of tyrosine phosphorylation. Tyrosine phosphorylation of p56Dok-2 occurs upon stimulation of cells with a variety of stimuli, or in cells transformed by oncogenic tyrosine kinases such as v-Src and Bcr-Abl (3-5). Based on the presence of several signaling domains (PH, PTB domain, tyrosine residue and proline-rich regions), it has been proposed that the p62dok family act as docking proteins that link RTKs to signal transduction pathways. p56Dok-2 has been proposed to be a negative regulator of cytokine-induced proliferation in T cells (5). Phosphorylated Tyr351 of p56Dok-2 mediates an association with the SH2 domain of Nck (4).

    1. Master, Z. et al. (2001) EMBO J. 20, 5919-5928.
    2. Grimm, J. et al. (2001) J. Cell. Biol. 154, 345-354.
    3. Cristofano, A. D. et al. (1998) J. Biol. Chem. 273, 4827-4830.
    4. Jones, N. and Dumont, D.J. (1999) Curr. Biol. 9, 1057-1060.
    5. Nemorin, J.G. and Duplay, P. (2000) J. Biol. Chem. 275, 14590-14597.
    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

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

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    图标文献和实验
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      祝贺〖上海雅裕 〗成为 Signalway Antibody 品牌 (SAB) 的独家总代理。 促销【 ABCD 】细则如下: 【 A 】 买两支 SAB 抗体免费获得 8G 优盘 活动时间:即日起,至 2011 年

    • 运用Cell Based Elisa检测信号通路蛋白和磷酸化蛋白

      using Phospho-p38 antibody (A) and Total-p38 antibody (B). Cell Based Elisa were performed directly in the 96-well plates using Phospho-p38 and Total-p38 antibodies (C). Figure 3: JNK detection with FACECells were serum-starved for 16 hours

    • 【共享】如何检测GFP、GFP、YFP、EYFP、CFP抗体?

      以及定位分析。那么该如何检测GFP其他的一些突变体,如EGFP、YFP、EYFP、CFP的表达和定位呢?我们来看一下GFP标签与其它突变体标签的关系。YFP(Yellow Fluorescent Protein)是黄色荧光蛋白,其序列与GFP基本相同。YFP就是把Thr203以Tyr取代,这样的GFP不发出绿色荧光,而发出较长波长的黄色荧光,也就是YFP。因此两者最大的区别则是发射波长了,在其他序列上没有区别。而EGFP是增强型的GFP,发生了双氨基酸取代,Leu(亮氨酸)取代GFP上的Phe64

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