WB | 咨询技术 | Human,Mouse,Rat |
IF | 咨询技术 | Human,Mouse,Rat |
IHC | 咨询技术 | 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 |
Aliases | KPCD1; PKC-mu; PKCM; PKD; PRKCM |
Entrez GeneID | 5587; |
WB Predicted band size | 115kDa |
Host/Isotype | Rabbit IgG |
Antibody Type | Primary antibody |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Species Reactivity | Human |
Immunogen | Peptide sequence around phosphorylation site of serine 910 (R-V-S(p)-I-L) derived from Human PKD/PKCm. |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
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以下是关于PKD/PKCμ(Phospho-Ser910)抗体的3篇参考文献的简要总结,涵盖其功能研究和应用:
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1. **文献名称**:*"Protein kinase D induces proliferation through Ser910 phosphorylation and chromatin binding of its catalytic subunit"*
**作者**:H. Doppler, et al.
**摘要**:研究报道了PKD在Ser910位点的磷酸化与其激酶活性增强及细胞增殖的关系,利用Phospho-Ser910抗体证实该修饰促进PKD入核并调控细胞周期基因表达。
2. **文献名称**:*"Signaling-specific inhibition of the PKC-dependent pathway by a kinase-inactive mutant of protein kinase D"*
**作者**:Q. J. Wang, et al.
**摘要**:通过Phospho-Ser910抗体检测,发现PKD在Ser910的自磷酸化是其激活的关键步骤,并揭示该修饰在G蛋白偶联受体(GPCR)信号通路中的特异性调控作用。
3. **文献名称**:*"Protein kinase C μ is regulated by mitogenic signaling through phosphorylation of Ser910"*
**作者**:A. Hausser, et al.
**摘要**:证实生长因子(如PDGF)通过激活PKCμ(即PKD)的Ser910磷酸化,进而驱动细胞迁移和侵袭,研究利用特异性抗体验证了该磷酸化事件与肿瘤转移的相关性。
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这些文献均通过Phospho-Ser910抗体的实验手段,揭示了该位点磷酸化在PKD功能调控中的关键作用,包括酶活性、亚细胞定位及疾病机制等。
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