| 货号 | 9371T |
| 反应种属 | Human,Mouse,Rat,Monkey, |
| 来源宿主 | Rabbit |
| 应用 | WB |
| 目标/特异性 | Phospho-PKC (pan) (βII Ser660) Antibody detects endogenous levels of PKC alphaα, β I, β II, δ, ε, η and θ isoforms only when phosphorylated at a carboxy-terminal residue homologous to serine 660 of PKC β II. This antibody does not detect PKC phosphorylated at other sites. |
| 使用方法 | WB(1:1000) |
| 供应商 | CST |
| 灵敏度 | Endogenous |
| 背景 | Activation of protein kinase C (PKC) is one of the earliest events in a cascade that controls a variety of cellular responses, including secretion, gene expression, proliferation, and muscle contraction (1,2). PKC isoforms belong to three groups based on calcium dependency and activators. Classical PKCs are calcium-dependent via their C2 domains and are activated by phosphatidylserine (PS), diacylglycerol (DAG), and phorbol esters (TPA, PMA) through their cysteine-rich C1 domains. Both novel and atypical PKCs are calcium-independent, but only novel PKCs are activated by PS, DAG, and phorbol esters (3-5). Members of these three PKC groups contain a pseudo-substrate or autoinhibitory domain that binds to substrate-binding sites in the catalytic domain to prevent activation in the absence of cofactors or activators. Control of PKC activity is regulated through three distinct phosphorylation events. Phosphorylation occurs in vivo at Thr500 in the activation loop, at Thr641 through autophosphorylation, and at the carboxy-terminal hydrophobic site Ser660 (2). Atypical PKC isoforms lack hydrophobic region phosphorylation, which correlates with the presence of glutamic acid rather than the serine or threonine residues found in more typical PKC isoforms. The enzyme PDK1 or a close relative is responsible for PKC activation. A recent addition to the PKC superfamily is PKCμ (PKD), which is regulated by DAG and TPA through its C1 domain. PKD is distinguished by the presence of a PH domain and by its unique substrate recognition and Golgi localization (6). PKC-related kinases (PRK) lack the C1 domain and do not respond to DAG or phorbol esters. Phosphatidylinositol lipids activate PRKs, and small Rho-family GTPases bind to the homology region 1 (HR1) to regulate PRK kinase activity (7). |
| 存放说明 | -20C |
| 计算分子量 | 78, 80, 82, 85 |
| 参考文献 | 1 . Nishizuka, Y. (1984) Nature 308, 693-8. 2 . Keranen, L.M. et al. (1995) Curr Biol 5, 1394-403. 3 . Mellor, H. and Parker, P.J. (1998) Biochem J 332 ( Pt 2), 281-92. 4 . Ron, D. and Kazanietz, M.G. (1999) FASEB J 13, 1658-76. 5 . Moscat, J. and Diaz-Meco, M.T. (2000) EMBO Rep 1, 399-403. 6 . Baron, C.L. and Malhotra, V. (2002) Science 295, 325-8. 7 . Flynn, P. et al. (2000) J Biol Chem 275, 11064-70. |
Western blot analysis of Baculovirus expressed PKC isoforms, using Phospho-PKC (pan) (βII Ser660) Antibody. 对Baculovirus表达的PKC亚型，使用Phospho-PKC (pan) (βII Ser660)抗体进行Western blot分析。 | |
Western blot analysis of extracts from TPA, Go6983 and/or Bisindolylmaleimide treated 293 cells, using Phospho-PKC (pan) (βII Ser660) Antibody. 对TPA、Go6983和/或Bisindolylmaleimide处理的293细胞，使用Phospho-PKC (pan) (βII Ser660)抗体进行Western blot分析。 | |
Western blot analysis of Baculovirus expressed PKCβ and PKCβ Ser660/Ala mutant, using Phospho-PKC (pan) (βII Ser660) Antibody (upper) or control PKCβ antibody (lower). 对Baculovirus转染的PKCβ和PKCβ Ser660/Ala突变体，使用Phospho-PKC (pan) (βII Ser660)抗体（上图）或对照PKCβ抗体（下图）进行Western blot分析。 |
