| 货号 | 62849S |
| 同种亚型 | Rabbit IgG |
| 反应种属 | Human, Mouse, Rat |
| 应用 | WB |
| 目标/特异性 | Na,K-ATPase β1 (D8W8J) Rabbit mAb recognizes endogenous levels of total Na,K-ATPase β1 protein. |
| 使用方法 | Western Blotting (1:1000) |
| 供应商 | CST |
| 灵敏度 | Endogenous |
| 背景 | The Na,K-ATPase is an integral membrane heterodimer belonging to the P-type ATPase family. This ion channel uses the energy derived from ATP hydrolysis to maintain membrane potential by driving sodium export and potassium import across the plasma membrane against their electrochemical gradients. It is composed of a catalytic α subunit and a β subunit (reviewed in 1). Several phosphorylation sites have been identified for the α1 subunit. Tyr10 is phosphorylated by an as yet undetermined kinase (2), Ser16 and Ser23 are phosphorylated by PKC, and Ser943 is phosphorylated by PKA (3-5). All of these sites have been implicated in the regulation of enzyme activity in response to hormones and neurotransmitters, altering trafficking and kinetic properties of Na,K-ATPase. Altered phosphorylation in response to angiotensin II stimulates activity in the rat proximal tubule (6). Na,K-ATPase is also involved in other signal transduction pathways. Insulin regulates its localization in differentiated primary human skeletal muscle cells, and this regulation is dependent on ERK1/2 phosphorylation of the α subunit (7). Na,K-ATPase and Src form a signaling receptor complex that affects regulation of Src kinase activity and, subsequently, its downstream effectors (8,9). Na,K-ATPase β1 is the non-catalytic subunit of Na,K-ATPase. It is required for stabilization, maturation, and translocation of the catalytic α subunit to the plasma membrane(10-12). Na,K-ATPase β1 also mediates the trans-dimerization of Na,K-ATPase between neighboring cells where it regulates the integrity of tight junctions (13-17). Glutathionylation of NA,K-ATPase β1 regulates the ion pump activity of Na,K-ATPase (18). Research studies have shown that Na,K-ATPase β1 is a target of the Sonic Hedgehog signaling pathway and may be involved in suppressing tumor development and progression (19). ATP1B1, the gene encoding Na,K-ATPase β1, is epigenetically silenced by promoter methylation in both renal cell carcinoma cell lines and patient tissues (20). |
| 计算分子量 | 45-55 |
| 参考文献 | 1 . Therien, A.G. and Blostein, R. (2000) Am J Physiol Cell Physiol 279, C541-66. 2 . Féraille, E. et al. (1999) Mol Biol Cell 10, 2847-59. 3 . Fisone, G. et al. (1994) J Biol Chem 269, 9368-73. 4 . Feschenko, M.S. and Sweadner, K.J. (1995) J Biol Chem 270, 14072-7. 5 . Beguin, P. et al. (1994) J Biol Chem 269, 24437-45. 6 . Yingst, D.R. et al. (2004) Am J Physiol Renal Physiol 287, F713-21. 7 . Al-Khalili, L. et al. (2004) J Biol Chem 279, 25211-8. 8 . Tian, J. et al. (2006) Mol Biol Cell 17, 317-26. 9 . Liang, M. et al. (2006) J Biol Chem 281, 19709-19. 10 . Beggah, A.T. et al. (1997) J Biol Chem 272, 10318-26. 11 . Hasler, U. et al. (1998) J Biol Chem 273, 30826-35. 12 . Rajasekaran, S.A. et al. (2004) Mol Biol Cell 15, 3224-32. 13 . Rajasekaran, S.A. et al. (2001) Mol Biol Cell 12, 3717-32. 14 . Rajasekaran, A.K. and Rajasekaran, S.A. (2003) Am J Physiol Renal Physiol 285, F388-96. 15 . Bab-Dinitz, E. et al. (2009) Biochemistry 48, 8684-91. 16 . Tokhtaeva, E. et al. (2011) J Biol Chem 286, 25801-12. 17 . Vagin, O. et al. (2012) Am J Physiol Cell Physiol 302, C1271-81. 18 . Figtree, G.A. et al. (2012) Free Radic Biol Med 53, 2263-8. 19 . Lee, S.J. et al. (2015) Mol Cancer 14, 159. 20 . Selvakumar, P. et al. (2014) Epigenetics 9, 579-86. |
Western blot analysis of extracts from human, mouse, and rat brains using Na,K-ATPase β1(D8W8J) Rabbit mAb. |
