Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb 产品图

Phospho-NF-κB p65 (Ser536) (93

H1) Rabbit mAb
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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2026年08月23日
  • western blot,免疫沉淀(IP),免疫荧光(IF),流式细胞(Flow Cyt)
  • 人,小鼠,大鼠,仓鼠,驴,猪,狗
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb

    • 应用范围

      western blot,免疫沉淀(IP),免疫荧光(IF),流式细胞(Flow Cyt)

    • 宿主

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 适应物种

      人,小鼠,大鼠,仓鼠,驴,猪,狗

    • 抗原来源

      /

    • 保质期

      详见说明书

    • 供应商

      CST

    • 是否单克隆

      单克隆

    • 保存条件

      -20°c

    Product Pathways - NF-kB Signaling

    Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb #3033

    Applications Reactivity Sensitivity MW (kDa) Isotype
    W IP IF-IC F H M R Hm Mk Pg (Dg) Endogenous 65 Rabbit IgG

    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 Dg=Dog Pg=Pig
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Protocols

    Specificity / Sensitivity

    Phospho-NF-kappaB p65 (Ser536) (93H1) Rabbit mAb detects NF-κB p65 only when phosphorylated at Ser536. It does not cross-react with the p50 subunit or other related proteins.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser536 of human NF-κB p65.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa and NIH/3T3 cells, untreated or TNF-α treated (#2169, 20 ng/ml for 5 minutes), using Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb (upper) or NF-κB p65 Antibody #3034 (lower).

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from THP-1 cells, differentiated with TPA (#9905, 80 nM for 24h) and treated with 1 μg/ml LPS for the indicated times, using Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb (upper) and NF-κB p65 (C22B4) Rabbit mAb #4764 (lower).

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of HeLa cells, untreated (blue) or TNF-α-treated (green), using Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb compared to a nonspecific negative control antibody (red).

    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of HeLa cells, untreated (left) and TNF-α treated (#8902 at 20 ng/ml for 20 min, right), using Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb (green). Actin filaments have been labeled with Alexa Fluor® phalloidin 555 (red).

    Background

    Transcription factors of the nuclear factor κ B (NF-κB)/Rel family play a pivotal role in inflammatory and immune responses (1,2). There are five family members in mammals: RelA, c-Rel, RelB, NF-κB1 (p105/p50), and NF-κB2 (p100/p52). Both p105 and p100 are proteolytically processed by the proteasome to produce p50 and p52, respectively. Rel proteins bind p50 and p52 to form dimeric complexes that bind DNA and regulate transcription. In unstimulated cells, NF-κB is sequestered in the cytoplasm by IκB inhibitory proteins (3-5). NF-κB-activating agents can induce the phosphorylation of IκB proteins, targeting them for rapid degradation through the ubiquitin-proteasome pathway and releasing NF-κB to enter the nucleus where it regulates gene expression (6-8). NIK and IKKα (IKK1) regulate the phosphorylation and processing of NF-κB2 (p100) to produce p52, which is then translocated to the nucleus (9-11).

    1. Baeuerle, P.A. and Henkel, T. (1994) Annu Rev Immunol 12, 141-79.
    2. Baeuerle, P.A. and Baltimore, D. (1996) Cell 87, 13-20.
    3. Haskill, S. et al. (1991) Cell 65, 1281-9.
    4. Thompson, J.E. et al. (1995) Cell 80, 573-82.
    5. Whiteside, S.T. et al. (1997) EMBO J 16, 1413-26.
    6. Traenckner, E.B. et al. (1995) EMBO J 14, 2876-83.
    7. Scherer, D.C. et al. (1995) Proc Natl Acad Sci USA 92, 11259-63.
    8. Chen, Z.J. et al. (1996) Cell 84, 853-62.
    9. Senftleben, U. et al. (2001) Science 293, 1495-9.
    10. Coope, H.J. et al. (2002) EMBO J 21, 5375-85.
    11. Xiao, G. et al. (2001) Mol Cell 7, 401-9.

    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

    Rabbit Monoclonals Produced Using Epitomics® Technology, U.S. Patent No. 5,675,063.


    For Research Use Only. Not For Use In Diagnostic Procedures.

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    图标文献和实验
    该产品被引用文献
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    [7]Geniposide protected against cerebral ischemic injury through the anti-inflammatory effect via the NF-κB signaling pathway.
    PMID:37333874Transl Neurosci2023-06-09
    [8]Daphnetin Preconditioning Decreases Cardiac Injury and Susceptibility to Ventricular Arrhythmia following Ischaemia-Reperfusion through the TLR4/MyD88/NF-Κb Signalling Pathway.
    PMID:33902056Pharmacology2021
    [9]Cryptotanshinone from Salvia miltiorrhiza Bunge (Danshen) inhibited inflammatory responses via TLR4/MyD88 signaling pathway.
    PMID:32158495Chin Med2020-03-15
    [10]Advanced Glycation End Products Enhance Macrophages Polarization into M1 Phenotype through Activating RAGE/NF-κB Pathway.
    PMID:26114112Biomed Res Int2015
    相关实验
    • 组化染色背景高?没信号?一篇文章带你快速掌握免疫组化!

      :使用 Anti-phospho-Akt (Ser473) Rabbit mAb 对石蜡包埋的人乳腺癌组织进行免疫组织化学分析。(图 A)使用免疫组化试剂盒M&R HRP/DAB Detection IHC Kit,抗体 1:100 稀释;(图 B) 采用普通免疫组化试剂盒,抗体 1:25 稀释。 图 6 免疫组化实验检测 Erk1/2 表达 注:使用 Anti-Erk1/2 Mouse mAb与p44/42 MAPK (Erk1/2)Rabbit mAb 对正常小鼠心脏组织进行免疫

    • 【求助】求助Western检测胞核中p65,需要内参吗,需要的话,选哪种

      llyun2000 我现在要做nf-kappaB的活性,请问,western检测细胞核中的p65,需内参吗? lwjssry 用组蛋白 H1、H2等 wangp249 Lamin A/C Lamin B hbqh 用β-actin可以吗 还想问用什么方法提细胞核啊? amygdala actin是典型的胞质内参

    • 【求助】再问几个NF-kB的问题

      http://www.dxy.cn/bbs/actions/archive/post/4320752_1.html http://www.takara.com.cn/activeproducts/am_2_04.htm 3、提高检索能力,多读文献吧,你的问题含糊,答案只能如此了。 4、NF-κB由两类亚基形成同源或异源二聚体。一类亚基包括p65(也称RelA)、RelB和C-Rel;另一类亚基包括p50和p52。最常见的NF-κB亚基组成形式为p65/p50或p65/p65

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