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Phospho-CDK2 (Thr160) Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月13日
  • W, IP, F, E-P
  • Rabbit
  • H,M,R
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-CDK2 (Thr160) Antibody

    • 抗原

      synthetic phosphopeptide corresponding to residues surrounding Thr160 of human CDK2

    • 应用范围

      W, IP, F, E-P

    • 宿主

      Rabbit

    • 库存

      大量

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 适应物种

      H,M,R

    • 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  IP=Immunoprecipitation  F=Flow Cytometry  E-P=ELISA (Peptide)
    Reactivity Key:  H=Human  M=Mouse  R=Rat
    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 F E-P H M R Endogenous 33 Rabbit
    Protocols
    Specificity / Sensitivity

    Phospho-CDK2 (Thr160) Antibody detects endogenous levels of CDK2 only when phosphorylated at threonine 160. The antibody weakly cross-reacts with cdc2 phosphorylated at Thr161. It does not cross-react with other phosphorylated cyclin dependent kinases.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Thr160 of human CDK2. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa cells synchronized in G0, G1/S or Mitosis, using Phospho-CDK2 (Thr160) Antibody.

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of untreated Jurkat cells, using Phospho-CDK2 (Thr160) Antibody versus propidium iodide (DNA content). The boxed population indicates phospho-CDK2 (Thr160)-positive cells.

    Background

    Cyclin-dependent kinase 2 (p33CDK2) is an important component of the cell cycle machinery. Like p34cdc2, kinase activity is regulated by phosphorylation state as well as association with a cyclin subunit and a CDK inhibitor. Inhibitory phosphorylation occurs on Thr14 and Tyr15 (1). Inhibition of CDK2-cyclin complexes can also be attributed to association with p27 Kip1 and p21 Waf1/Cip1 (2). Activation of CDK2 complexes requires dephosphorylation of Thr14 and Tyr15 by cdc25 phosphatase and phosphorylation of Thr160 (3), which is mediated by CAK, a complex of CDK7 and cyclin H (4). CDK2/cyclin E kinase activity is important for the G1 to S transition and phosphorylation of the Rb protein. During S-phase, active CDK2/cyclin A complexes predominate and phosphorylate E2F and the active CDK2 complex persists in the nucleus throughout G2 (5).

    1. Morgan, D.O. (1995) Nature 374, 131-134.
    2. Poon, R.Y. et al. (1996) J. Biol. Chem. 271, 13283-13291.
    3. Gu, Y. et al. (1992) EMBO J. 11, 3995-4005.
    4. Fesquet, D. et al. (1993) EMBO J. 12, 3111-3121.
    5. Morgan, D.O. (1997) Annu. Rev. Cell Dev. Biol. 13, 261-291.
    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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