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Phospho-p38 MAPK (Thr180/Tyr18

2) (3D7) Rabbit mAb
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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月31日
  • W, IF-IC, F
  • H,M,R,Mk,Dm,Pg,Sc,Hm,B
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-p38 MAPK (Thr180/Tyr182) (3D7) Rabbit mAb

    • 抗原

      synthetic phosphopeptide corresponding to residues surrounding Thr180/Tyr182 of human p38 MAPK

    • 应用范围

      W, IF-IC, F

    • 适应物种

      H,M,R,Mk,Dm,Pg,Sc,Hm,B

    • 供应商

      CST

    • 库存

      大量

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      200 ul (20 western blots)/600 ul (60 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:200 ul (20 western blots)产品价格:¥请询价
    规格:600 ul (60 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  IF-IC=Immunofluorescence (Immunocytochemistry)  F=Flow Cytometry
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Hm=Hamster  Mk=Monkey  Dm=D. melanogaster  Z=Zebrafish  B=Bovine  Pg=Pig  Sc=S. cerevisiae
    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 IF-IC F H M R Mk Dm Pg Sc (Hm) (B) Endogenous 43 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    Phospho-p38 MAP Kinase (Thr180/Tyr182) (3D7) Rabbit mAb detects endogenous levels of p38 MAPK only when dually phosphorylated at Thr180 and Tyr182. This antibody does not cross-react with the phosphorylated forms of either p42/44 MAPK or SAPK/JNK.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Thr180/Tyr182 of human p38 MAPK.

    Western Blotting

    Western Blotting

    Specificity of Phospho-Erk1/2, Phospho-p38 MAPK and Phospho-SAPK/JNK Rabbit mAb: Western blot analysis of extracts from NIH/3T3 cells treated with PDGF and UV, using Phospho-p38 MAPK Rabbit mAb #9215, Phospho-SAPK/JNK Rabbit mAb and Phospho-Erk1/2 Rabbit mAb.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from Jurkat, C6, NIH/3T3 and COS cells, untreated or treated as indicated, using Phospho-p38 MAPK (Thr180/Tyr182) (3D7) Rabbit mAb (upper) or p38 MAPK Antibody #9212 (lower).

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of Jurkat cells, untreated (blue) or anisomycin-treated (green), using Phospho-p38 MAPK (Thr180/Tyr182) (3D7) Rabbit mAb compared to a nonspecific negative control antibody (red).


    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of HeLa cells, untreated (left) or anisomycin-treated (right), using Phospho-p38 MAPK (Thr180/Tyr182)(3D7) Rabbit mAb (green). Actin filaments have been labeled with Alexa Fluor® 555 phalloidin (red).

    Background

    p38 MAP kinase (MAPK), also called RK (1) or CSBP (2), is the mammalian orthologue of the yeast HOG kinase that participates in a signaling cascade controlling cellular responses to cytokines and stress (1-4). Four isoforms of p38 MAPK, p38α, β, γ (also known as Erk6 or SAPK3), and δ (also known as SAPK4) have been identified. Similar to the SAPK/JNK pathway, p38 MAPK is activated by a variety of cellular stresses including osmotic shock, inflammatory cytokines, lipopolysaccharide (LPS), UV light, and growth factors (1-5). MKK3, MKK6, and SEK activate p38 MAPK by phosphorylation at Thr180 and Tyr182. Activated p38 MAPK has been shown to phosphorylate and activate MAPKAP kinase 2 (3) and to phosphorylate the transcription factors ATF-2 (5), Max (6), and MEF2 (5-8).SB203580 (4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)-imidazole) is a selective inhibitor of p38 MAPK. This compound inhibits the activation of MAPKAPK-2 by p38 MAPK and subsequent phosphorylation of HSP27 (9). SB203580 inhibits p38 MAPK catalytic activity by binding to the ATP-binding pocket, but does not inhibit phosphorylation of p38 MAPK by upstream kinases (10).

    1. Rouse, J. et al. (1994) Cell 78, 1027-1037.
    2. Han, J. et al. (1994) Science 265, 808-811.
    3. Lee, J.C. et al. (1994) Nature 372, 739-746.
    4. Freshney, N.W. et al. (1994) Cell 78, 1039-1049.
    5. Raingeaud, J. et al. (1995) J. Biol. Chem. 270, 7420-7426.
    6. Zervos, A.S. et al. (1995) Proc. Natl. Acad. Sci. USA 92, 10531-10534.
    7. Zhao, M. et al. (1999) Mol. Cell. Biol. 19, 21-30.
    8. Yang, S.H. et al. (1999) Mol. Cell. Biol. 19, 4028-4038.
    9. Cuenda, A. et al. (1995) FEBS Lett 364, 229-33.
    10. Kumar, S. et al. (1999) Biochem Biophys Res Commun 263, 825-31.
    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
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      results of phosphorylated proteins磷酸化的试剂盒中的抗体是经过大量筛选,选取了高特异性和低背景的抗体。p-P38MAPK抗体是基于P38的磷酸化Thr180Tyr182这个位点多肽片段所制备。P-JNK抗体是基于人的Thr183和Tyr185.这个抗体可以同时识别P-JNK1和P-JNK2.我们在运用Cell Based Elisa P38和JNK两个试剂盒做检测的同时,又用传统的WB方式来验证这个结果。经过反复验证,都得出了同样的结果, Cell Based

    • 运用Cell Based Elisa检测信号通路蛋白和磷酸化蛋白

      results of phosphorylated proteins磷酸化的试剂盒中的抗体是经过大量筛选,选取了高特异性和低背景的抗体。p-P38MAPK抗体是基于P38的磷酸化Thr180Tyr182这个位点多肽片段所制备。P-JNK抗体是基于人的Thr183和Tyr185.这个抗体可以同时识别P-JNK1和P-JNK2.我们在运用Cell Based Elisa P38和JNK两个试剂盒做检测的同时,又用传统的WB方式来验证这个结果。经过反复验证,都得出了同样的结果,Cell Based Elisa

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