TBC1D1 (V796) Antibody

TBC1D1 (V796) Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年10月23日
  • W, IP
  • Rabbit
  • M
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    • 详细信息
    • 技术资料
    • 抗体英文名

      TBC1D1 (V796) Antibody

    • 抗原

      synthetic peptide corresponding to the sequence around Val796 of mouse TBC1D1

    • 应用范围

      W, IP

    • 宿主

      Rabbit

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 适应物种

      M

    • 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  IP=Immunoprecipitation
    Reactivity Key:  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 IP M Endogenous 160 Rabbit
    Protocols
    Specificity / Sensitivity

    TBC1D1 (V796) Antibody detects endogenous levels of total TBC1D1 protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the sequence around Val796 of mouse TBC1D1. Antibodies are purified by protein A and peptide affinity chromatography.

    TBC1D1 (V796) Antibody

    Western blot analysis of extracts from C2C12 myotubes using TBC1D1 (V796) Antibody.

    Background

    TBC1D1 is a paralog of AS160 (1) and both proteins share about 50% identity (2). TBC1D1 was shown to be a candidate gene for severe obesity (3). It plays a role in Glut4 translocation through its GAP activity (2,4). Studies indicate that TBC1D1 is highly expressed in skeletal muscle (1). Insulin, AICAR, and contraction directly regulate TBC1D1 phosphorylation in this tissue (1). Three AMPK phosphorylation sites (Ser231, Ser660, and Ser700) and one Akt phosphorylation site (Thr590) were identified (5). Muscle contraction or AICAR treatment increases phosphorylation on Ser231, Ser660, and Ser700 but not on Thr590; insulin increases phosphorylation on Thr590 only (5).

    1. Taylor, E.B. et al. (2008) J Biol Chem 283, 9787-96.
    2. Roach, W.G. et al. (2007) Biochem J 403, 353-8.
    3. Stone, S. et al. (2006) Hum Mol Genet 15, 2709-20.
    4. Chavez, J.A. et al. (2008) J Biol Chem 283, 9187-95.
    5. Vichaiwong, K. et al. (2010) Biochem J 431, 311-20.
    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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