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TAZ (V386) Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年11月19日
  • W
  • Rabbit
  • H,M,R,Hr
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      TAZ (V386) Antibody

    • 抗原

      synthetic peptide corresponding to amino acid residues surrounding Val 386 of human TAZ

    • 应用范围

      W

    • 宿主

      Rabbit

    • 级别

      详见MSDS文件

    • 供应商

      CST

    • 库存

      大量

    • 适应物种

      H,M,R,Hr

    • 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  R=Rat  Hr=Horse
    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 (Hr) Endogenous 50 Rabbit
    Protocols
    Specificity / Sensitivity

    TAZ (V386) Antibody detects endogenous levels of total TAZ protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to amino acid residues surrounding Val 386 of human TAZ. Antibodies are purified by Protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines using TAZ (V386) Antibody.

    Background

    TAZ is a transcriptional co-activator with a PDZ-binding motif that is regulated by its interaction with 14-3-3 proteins (1). TAZ shares homology with the WW domain of Yes-associated protein (YAP) (1). TAZ is proposed to modulate the switch between proliferation and differentiation of mesenchymal stem cells (MSC) via interaction with transcription factors Runx2 and PPARγ. This process is critical to normal tissue development and the prevention of tumor formation. Due to its role in determination of MSC fate, TAZ may have clinical relevance to several human diseases caused by an imbalance of MSC differentiation (2,3). TAZ appears to be negatively regulated by LATS tumor suppressor kinase, a component of the Hippo pathway that controls tissue growth and tumor development (4).

    1. Kanai, F. et al. (2000) EMBO J 19, 6778-91.
    2. Hong, J.H. et al. (2005) Science 309, 1074-8.
    3. Hong, J.H. and Yaffe, M.B. (2006) Cell Cycle 5, 176-9.
    4. Lei, Q.Y. et al. (2008) Mol Cell Biol 28, 2426-36.
    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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    • STM:广州医科大学刘铭/谢茂彬合作发现​肝细胞癌的新潜在治疗靶点 Claudin 6

      组于 Science Translational Medicine 杂志(STM)在线发表题为 Targeting tumor lineage plasticity in hepatocellular carcinoma using an anti-CLDN6 antibody-drug conjugate 的研究论文。这项研究揭示了细胞紧密连接(tight junction)蛋白 Claudin 6 通过调控肝癌细胞的谱系可塑性(lineage plasticity),促进肝癌进展与耐药的机制,并初步报道

    • 【转帖】Top 100 proteomics publications

      replication through telomeres requires Taz1. Nature 10. Wang et al. (2006) Hsp90 Cochaperone Aha1 Downregulation Rescues Misfolding of CFTR in Cystic Fibrosis. Cell 11. Olsen et al. (2006) Global, In Vivo, and Site-Specific Phosphorylation Dynamics

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