Phospho-TAK1 (Thr184/187) Antibody

Phospho-TAK1 (Thr184/187) Anti

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年10月11日
  • W
  • Rabbit
  • H,M,R,C,X,Z,B
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    • 详细信息
    • 技术资料
    • 抗体英文名

      Phospho-TAK1 (Thr184/187) Antibody

    • 抗原

      phosphopeptide corresponding to residues surrounding Thr184 and Thr187 of human TAK1

    • 应用范围

      W

    • 宿主

      Rabbit

    • 适应物种

      H,M,R,C,X,Z,B

    • 库存

      大量

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 供应商

      CST

    • 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  R=Rat  C=Chicken  X=Xenopus  Z=Zebrafish  B=Bovine
    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) (R) (C) (X) (Z) (B) Endogenous 82 Rabbit
    Protocols
    Specificity / Sensitivity

    Phospho-TAK1 (Thr184/187) Antibody detects endogenous levels of TAK1 only when phosphorylated at both threonine 184 and threonine 187. This antibody weakly cross-reacts with TAK1 singly phosphorylated at threonine 184.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a phosphopeptide corresponding to residues surrounding Thr184 and Thr187 of human TAK1. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from 293 IL-1R cells treated with IL-1alpha (20 ng/ml) or IL-1beta (10 ng/ml) and Calyculin A (50 nM) for 10 minutes, using Phospho-TAK1 (Thr184/187) Antibody.

    Background

    TAK1 is a mitogen-activated protein kinase kinase kinase that can be activated by TGF-β, bone morphogenetic protein and other cytokines including IL-1 (1,2). In vivo activation of TAK1 requires association with TAK1 binding protein 1 (TAB1), which triggers phosphorylation of TAK1 (3,4). Another adaptor protein, TAB2, links TAK1 with TRAF6 and mediates TAK1 activation upon IL-1 stimulation (5). Once activated, TAK1 phosphorylates MAPK kinases MKK4 and MKK3/6, which activate p38 MAPK and JNK, respectively. In addition, TAK1 activates the NF-κB pathway by interacting with TRAF6 and phosphorylating the NF-κB inducing kinase (NIK) (2).

    TAK1 activation requires multiple phosphorylations in its activation loop. Mutations of Thr187 and Thr184, residues located in the activation loop of TAK1, impairs phosphorylation of both TAK1 and TAB1 and reduces the kinase activity of TAK1, suggesting that autophosphorylation of these residues is necessary for TAK1 activation (4).

    1. Yamaguchi, K. et al. (1995) Science 270, 2008-2011.
    2. Ninomiya-Tsuji, J. et al. (1999) Nature 398, 252-256.
    3. Shibuya, H. et al. (1996) Science 272, 1179-1182.
    4. Sakurai, H. et al. (2000) FEBS Lett. 474, 141-145.
    5. Takaesu, G. et al. (2000) Mol. Cell 4, 649-658.
    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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