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Phospho-Rb (Ser807/811) Antibo

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年10月10日
  • W, IP, IHC-P
  • Rabbit
  • H,R,Mk,M
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-Rb (Ser807/811) Antibody

    • 抗原

      synthetic phosphopeptide corresponding to residues around Ser807/811 of human Rb

    • 应用范围

      W, IP, IHC-P

    • 宿主

      Rabbit

    • 库存

      大量

    • 保质期

      详见说明书

    • 适应物种

      H,R,Mk,M

    • 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

      40 ul (4 western blots)/100 ul (10 western blots)/300 ul (30 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:40 ul (4 western blots)产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:300 ul (30 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  IHC-P=Immunohistochemistry (Paraffin)
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey
    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 IHC-P H R Mk (M) Endogenous 110 Rabbit
    Protocols
    Specificity / Sensitivity

    Phospho-Rb (Ser807/811) Antibody detects endogenous levels of Rb when phosphorylated at serine 807/811. The antibody may cross-react with Rb phosphorylated at Ser608.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues around Ser807/811 of human Rb. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from human fibroblasts synchronized by serum deprivation, using Phospho-Rb (Ser807/811) Antibody. Cells were synchronized for 24 hours then released by addition of serum and harvested at the times indicated. Cell cycle progression was verified by cyclin analysis and FACS. (Provided by John Boylan, Dupont/Merck, Delaware.)

    Background

    The retinoblastoma tumor suppressor protein, Rb, regulates cell proliferation by controlling progression through the restriction point within the G1-phase of the cell cycle (1). Rb has three functionally distinct binding domains and interacts with critical regulatory proteins including the E2F family of transcription factors, c-Abl tyrosine kinase, and proteins with a conserved LXCXE motif (2-4). Cell cycle-dependent phosphorylation by a CDK inhibits Rb target binding and allows cell cycle progression (5). Rb inactivation and subsequent cell cycle progression likely requires an initial phosphorylation by cyclin D-CDK4/6 followed by cyclin E-CDK2 phosphorylation (6). Specificity of different CDK/cyclin complexes has been observed in vitro (6-8) and cyclin D1 is required for Ser780 phosphorylation in vivo (9).

    1. Sherr, C.J. (1996) Science 274, 1672-7.
    2. Nevins, J.R. (1992) Science 258, 424-9.
    3. Welch, P.J. and Wang, J.Y. (1993) Cell 75, 779-90.
    4. Hu, Q.J. et al. (1990) EMBO J 9, 1147-55.
    5. Knudsen, E.S. and Wang, J.Y. (1997) Mol Cell Biol 17, 5771-83.
    6. Lundberg, A.S. and Weinberg, R.A. (1998) Mol Cell Biol 18, 753-61.
    7. Connell-Crowley, L. et al. (1997) Mol Biol Cell 8, 287-301.
    8. Kitagawa, M. et al. (1996) EMBO J 15, 7060-9.
    9. Geng, Y. et al. (2001) Proc Natl Acad Sci USA 98, 194-9.
    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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    • Optimized Protocol to Make Phospho-Specific Antibodies that Work

      , not simply its level of expression. In this review, we will discuss both the design of the phosphopeptide immunogen and immunization. The affinity purification of the phospho-specific antibody as well as the methods most suitable for characterizing

    • Using Phospho‐Motif Antibodies to Determine Kinase Substrates

      comprising both the phosphorylated residue and the surrounding residues that determine kinase specificity, with degenerate residues taking up the remaining positions. Currently, several categories of phospho?motif antibody are commercially available

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