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Phospho-IκBε (Ser18/22) Antibo

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月28日
  • W
  • Rabbit
  • H,M,R,B,Dg
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-IκBε (Ser18/22) Antibody

    • 抗原

      synthetic phosphopeptide corresponding to residues surrounding serine 18/22 of human IκBε

    • 应用范围

      W

    • 宿主

      Rabbit

    • 适应物种

      H,M,R,B,Dg

    • 级别

      详见MSDS文件

    • 保质期

      详见说明书

    • 库存

      大量

    • 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
    Reactivity Key:  H=Human  M=Mouse  R=Rat  B=Bovine  Dg=Dog
    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 (B) (Dg) Endogenous 45 Rabbit
    Protocols
    Specificity / Sensitivity

    Phospho-IκBε (Ser18/22) Antibody detects endogenous levels of IκBε only when phosphorylated at serines 18 and 22. No cross-reactivity was detected with other family members at physiological conditions.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding serine 18/22 of human IκBε. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from 293 cells treated with TNF-α (20 ng/ml) for the indicated times, using Phospho-IκBε (Ser18/22) Antibody.

    Background

    The NF-κB/Rel transcription factors are present in the cytosol in an inactive state complexed with the inhibitory IκB proteins (1-3). Activation occurs via phosphorylation of IκBα at Ser32 and Ser36 followed by proteasome-mediated degradation that results in the release and nuclear translocation of active NF-κB (3-7). IκBα phosphorylation and resulting Rel-dependent transcription are activated by a highly diverse group of extracellular signals including inflammatory cytokines, growth factors, and chemokines. Kinases that phosphorylate IκB at these activating sites have been identified (8).

    The regulation of IκBβ and IκBε is similar to that of IκBα. However, the phosphorylation and ubiquitin-mediated degradation of these proteins occurs with much slower kinetics (9). IKK phosphorylation of IκBβ occurs at Ser19 and Ser23, while IκBε can be phosphorylated at Ser18 and Ser22 (10).

    1. Baeuerle, P.A. and Baltimore, D. (1988) Science 242, 540-6.
    2. Beg, A.A. and Baldwin, A.S. (1993) Genes Dev 7, 2064-70.
    3. Finco, T.S. et al. (1994) Proc Natl Acad Sci USA 91, 11884-8.
    4. Brown, K. et al. (1995) Science 267, 1485-8.
    5. Brockman, J.A. et al. (1995) Mol Cell Biol 15, 2809-18.
    6. Traenckner, E.B. et al. (1995) EMBO J 14, 2876-83.
    7. Chen, Z.J. et al. (1996) Cell 84, 853-62.
    8. Karin, M. and Ben-Neriah, Y. (2000) Annu Rev Immunol 18, 621-63.
    9. Hoffmann, A. et al. (2002) Science 298, 1241-1245.
    10. Shirane, M. et al. (1999) J. Biol. Chem. 274, 28169-28174.
    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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    • secondary antibody review -- data from 99 publications

      Signaling 18   IgG   Alexa Fluor 488 immunocytochemistry 1:2000     18   IgG   Alexa Fluor 568 immunocytochemistry 1:2000     19 donkey IgG   HRP western blot 1:3000 detect antibody binding in mouse epithelial cells Amersham Biosciences 19 goat

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