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Rabbit Polyclonal JNK1/JNK2/JNK3(phospho-Thr183/Tyr185) Antibody

  • 中文名: JNK1/JNK2/JNK3(phospho-Thr183/Tyr185)抗体
  • 别    名: Stress-activated protein kinase JNK1; c-Jun N-terminal kinase 1; JNK-46
货号: IPDX40304
Price: ¥1280
数量:
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验证与应用

应用及物种
WB 咨询技术 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 1/50-300 Human,Mouse,Rat
ICC 1/100-1/200 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesStress-activated protein kinase JNK1; c-Jun N-terminal kinase 1; JNK-46
Entrez GeneID5599;
WB Predicted band size46 54 kDa
Host/IsotypeRabbit IgG
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman,Mouse,Rat
ImmunogenPeptide sequence around phosphorylation site of Thr183/Tyr185 (M-M-T(p)-P-Y(p)- V - V ) derived from Human JNK1/JNK2/JNK3.
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是关于JNK1/JNK2/JNK3 (phospho-Thr183/Tyr185) 抗体的参考文献示例,按文献名称、作者和摘要内容简要概括:

1. **"A conserved kinase cascade for MAP kinase activation in yeast"**

*作者:Davis, R.J. (1994)*

摘要:该研究首次阐明了JNK(c-Jun N-terminal kinase)的激活机制,指出Thr183和Tyr185双磷酸化是JNK激酶活性调控的关键步骤,并开发了特异性识别该磷酸化位点的抗体以验证JNK在应激信号通路中的作用。

2. **"Selective interaction of JNK protein kinase isoforms with transcription factors"**

*作者:Gupta, S. et al. (1996)*

摘要:通过使用phospho-Thr183/Tyr185特异性抗体,作者揭示了JNK1、JNK2和JNK3在不同细胞类型中的激活差异,并证明其磷酸化状态与底物蛋白(如c-Jun)的结合能力直接相关。

3. **"Absence of excitotoxicity-induced apoptosis in the hippocampus of mice lacking the Jnk3 gene"**

*作者:Yang, D.D. et al. (1997)*

摘要:利用磷酸化特异性抗体检测JNK3在神经细胞中的激活状态,发现JNK3的Thr183/Tyr185磷酸化是介导谷氨酸兴奋性毒性诱导细胞凋亡的必要条件,为神经退行性疾病机制提供了关键证据。

4. **"Mammalian MAP kinase modules: how to transduce specific signals"**

*作者:Tournier, C. et al. (2001)*

摘要:通过Western blot和免疫沉淀实验,验证了JNK1/2/3在紫外线辐射和炎症因子刺激下的磷酸化模式,强调phospho-Thr183/Tyr185抗体在检测MAPK通路动态激活中的重要性。

这些文献涵盖了该抗体在信号通路机制、疾病模型及激酶功能研究中的典型应用。

背景信息

The c-Jun N-terminal kinase (JNK) family, comprising JNK1 (MAPK8), JNK2 (MAPK9), and JNK3 (MAPK10), is a subgroup of mitogen-activated protein kinases (MAPKs) central to cellular stress responses, apoptosis, inflammation, and differentiation. Activation of JNKs requires dual phosphorylation at conserved Thr183 and Tyr185 residues within the activation loop. Antibodies targeting phospho-Thr183/Tyr185 (p-JNK) are critical tools for detecting activated JNK isoforms in research. These antibodies recognize all three JNK isoforms when phosphorylated at these sites, making them pan-specific for monitoring JNK activation across biological contexts. However, distinguishing between isoforms (JNK1/2 vs. JNK3) often requires additional validation via isoform-specific antibodies or genetic knockdown. JNK1 and JNK2 are ubiquitously expressed, while JNK3 is primarily neuronal. The phosphorylation-dependent activation of JNKs is triggered by upstream kinases (MKK4/7) in response to stressors like UV radiation, cytokines, or oxidative stress. p-JNK antibodies are widely used in Western blotting, immunohistochemistry, and flow cytometry to study signaling dynamics in diseases such as neurodegeneration, cancer, and metabolic disorders. Researchers must validate antibody specificity using knockout controls or phosphatase treatment to confirm phosphorylation-dependent signals. Molecular weight differences (JNK1/2 ~46 kDa, JNK3 ~55 kDa) aid in isoform identification during analysis.

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