| 货号 | 4026S |
| 反应种属 | Human/Mouse/Rat/Hamster/MonkeyDog |
| 来源宿主 | Rabbit |
| 应用 | W/IF-IC |
| 目标/特异性 | α-Parvin Antibody detects endogenous levels of total α-parvin protein. |
| 使用方法 | WB(1:1000) IF-IC (1:400) |
| 供应商 | CST |
| 灵敏度 | Endogenous |
| 背景 | The extracellular matrix (ECM) is a complex structure of secreted macromolecules surrounding mammalian organs and tissues. Controlled interactions between cells and the ECM are important in proliferation, migration, survival, polarity, and differentiation. Cells contact the ECM primarily through heterodimeric integral membrane proteins called integrins. Integrins connect the ECM to the cytoskeleton, and therefore the cell signaling machinery, through protein complexes called focal adhesions (1). The ILK/PINCH/Parvin (IPP) complex is composed of three highly conserved proteins recruited to sites of ECM contact as pre-assembled structures. The IPP acts at the interface of the integrin/actin connection to regulate formation of focal adhesions and integrin signaling. All three proteins contain multiple protein binding domains allowing them to function as adaptor proteins in the formation of focal adhesions. ILK (integrin-linked kinase) also has a catalytic (protein Ser/Thr kinase) domain, and may or may not function as a kinase in vivo. Roles for IPP proteins outside of the IPP complex have been proposed, including regulation of gene expression (2,3). The parvin family consists of 3 members, α-parvin/actopaxin, β-parvin/affixin, and γ-parvin. α-parvin and β-parvin are expressed ubiquitously, while expression of γ-parvin is restricted to hematopoietic cells (4). α-parvin binds to f-actin both directly and via interaction with the focal adhesion protein paxillin (5). α-parvin regulates cell spreading and motility through interactions with the cofilin kinase TESK1 (6), and with the GTPase activating protein CdGAP (7). Phosphorylation of α-parvin during mitosis may have a role in the regulation of actin dynamics during the cell cycle (8). |
| 存放说明 | -20C |
| 计算分子量 | 43 |
| 参考文献 | 1 . Burridge, K. et al. (1988) Annu Rev Cell Biol 4, 487-525. 2 . Legate, K.R. et al. (2006) Nat Rev Mol Cell Biol 7, 20-31. 3 . Wu, C. (2004) Biochim Biophys Acta 1692, 55-62. 4 . Korenbaum, E. et al. (2001) Gene 279, 69-79. 5 . Nikolopoulos, S.N. and Turner, C.E. (2000) J Cell Biol 151, 1435-48. 6 . LaLonde, D.P. et al. (2005) J Biol Chem 280, 21680-8. 7 . LaLonde, D.P. et al. (2006) Curr Biol 16, 1375-85. 8 . Curtis, M. et al. (2002) Biochem J 363, 233-42. |
Western blot analysis of extracts from various cell types using α-Parvin Antibody. In lane 2, HeLa cells were isolated in mitosis by mitotic shake-off following nocodozole treatment (100 ng/mL for 4 hours).使用α-Parvin 抗体对多种细胞提取物进行western blot分析。在第二道，使用有丝分裂摇落法随后进行nocodozole处理（100 ng/mL 4小时）获得有丝分裂期的HeLa细胞。 | |
Confocal immunofluorescent analysis of HeLa cells using α-Parvin Antibody (green). Actin filaments have been labeled with DY-554 phalloidin (red). Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye).使用 α-Parvin抗体对HeLa细胞进行激光共聚焦免疫荧光分析（绿色）。肌动蛋白丝使用DY-554鬼笔环肽（红色）标记。蓝色加色=DRAQ5® #4084 （DNA荧光染料）。 |
