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RIP (D94C12) XP Rabbit mAb__

®
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  • 询价
  • Cell Signaling Technology已认证
  • 3493
  • USA
  • 2025年09月07日
  • W, IP, IF-IC, F
  • H,M,R,Hm,Mk
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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 抗体英文名

      RIP (D94C12) XP Rabbit mAb__®

    • 抗原

      synthetic peptide corresponding to residues surrounding Leu190 of human RIP

    • 应用范围

      W, IP, IF-IC, F

    • 适应物种

      H,M,R,Hm,Mk

    • 供应商

      CST

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      40 ul (4 western blots)/100 ul (10 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: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  IF-IC=Immunofluorescence (Immunocytochemistry)  F=Flow Cytometry
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Hm=Hamster  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) Isotype
    W IP IF-IC F H M R Hm Mk Endogenous 78 Rabbit
    Protocols
    Specificity / Sensitivity

    RIP (D94C12) XP® Rabbit mAb detects endogenous levels of total RIP (RIP1) protein. It has not been shown to cross-react with other RIP family members.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Leu190 of human RIP.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines using RIP (D94C12) XP® Rabbit mAb.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa cells, untransfected or transfected with human RIP construct, using RIP (D94C12) XP® Rabbit mAb.

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of MCF7 cells using RIP (D94C12) XP® Rabbit mAb (blue) compared to Rabbit (DA1E) mAb IgG XP® Isotype Control #3900 (red).


    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of OVCAR8 cells using RIP (D94C12) XP® Rabbit mAb (green). Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye).

    Background

    The RIP (receptor-interacting protein) family of serine-threonine kinases (RIP, RIP2, RIP3 and RIP4) are important regulators of cellular stress that can trigger pro-survival and inflammatory responses through the activation of NF-κB as well as pro-apoptotic pathways (1). In addition to the kinase domain, RIP contains a death domain responsible for interaction with the death domain receptor Fas and for the recruitment to TNFR1 through interaction with TRADD (2,3). RIP also interacts with TNF-receptor-associated factors (TRAFs) and can recruit IKKs to the TNFR1 signaling complex via interaction with NEMO leading to IκB phosphorylation and degradation (6,7). Overexpression of RIP induces both NF-κB activation and apoptosis (2,3). Caspase-8 dependent cleavage of the death domain on RIP can trigger the apoptotic activity of RIP (8). RIP-deficient cells show a failure in TNF-mediated NF-κB activation making the cells more sensitive to apoptosis (4,5).

    1. Meylan, E. and Tschopp, J. (2005) Trends Biochem Sci 30, 151-9.
    2. Hsu, H. et al. (1996) Immunity 4, 387-96.
    3. Stanger, B.Z. et al. (1995) Cell 81, 513-23.
    4. Ting, A.T. et al. (1996) EMBO J 15, 6189-96.
    5. Kelliher, M.A. et al. (1998) Immunity 8, 297-303.
    6. Devin, A. et al. (2000) Immunity 12, 419-29.
    7. Zhang, S.Q. et al. (2000) Immunity 12, 301-11.
    8. Lin, Y. et al. (1999) Genes Dev 13, 2514-26.
    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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