| 货号 | 2500T |
| 同种亚型 | Rabbit IgG |
| 反应种属 | Human/D.melanogaster/Bovine/Pig |
| 来源宿主 | Rabbit |
| 应用 | W/IP/IF-IC/F |
| 目标/特异性 | VE-Cadherin (D87F2) XP® Rabbit mAb recognizes endogenous levels of total VE-cadherin protein. The antibody does not cross-react with other cadherin family proteins. |
| 使用方法 | WB(1:1000) IP (1:50) F (1:100) IF-IC (1:400) |
| 供应商 | CST |
| 灵敏度 | Endogenous |
| 背景 | Cadherins are a superfamily of transmembrane glycoproteins that contain cadherin repeats of approximately 100 residues in their extracellular domain. Cadherins mediate calcium-dependent cell-cell adhesion and play critical roles in normal tissue development (1). The classic cadherin subfamily includes N-, P-, R-, B- and E-cadherins as well as about ten other members that are found in adherens junctions, a cellular structure near the apical surface of polarized epithelial cells. The cytoplasmic domain of classical cadherins interacts with β-catenin, γ-catenin (also called plakoglobin), and p120 catenin. β-catenin and γ-catenin associate with α-catenin, which links the cadherin-catenin complex to the actin cytoskeleton (1,2). While β- and γ-catenin play structural roles in the junctional complex, p120 regulates cadherin adhesive activity and trafficking (1-4). E-cadherin is considered an active suppressor of invasion and growth of many epithelial cancers (1-3). Recent studies indicate that cancer cells have up-regulated N-cadherin in addition to loss of E-cadherin. This change in cadherin expression is called the "cadherin switch". N-cadherin cooperates with the FGF receptor, leading to over-expression of MMP-9 and cellular invasion (3). In endothelial cells, VE-cadherin signaling, expression, and localization correlate with vascular permeability and tumor angiogenesis (5,6). Expression of P-cadherin, which is normally present in epithelial cells, is also altered in ovarian and other human cancers (7,8). |
| 存放说明 | -20C |
| 计算分子量 | 130-140 |
| 参考文献 | 1 . Wheelock, M.J. and Johnson, K.R. (2003) Annu Rev Cell Dev Biol 19, 207-35. 2 . Christofori, G. (2003) EMBO J 22, 2318-23. 3 . Hazan, R.B. et al. (2004) Ann N Y Acad Sci 1014, 155-63. 4 . Bryant, D.M. and Stow, J.L. (2004) Trends Cell Biol 14, 427-34. 5 . Rabascio, C. et al. (2004) Cancer Res 64, 4373-7. 6 . Yamaoka-Tojo, M. et al. (2006) Arterioscler Thromb Vasc Biol 26, 1991-7. 7 . Patel, I.S. et al. (2003) Int J Cancer 106, 172-7. 8 . Sanders, D.S. et al. (2000) J Pathol 190, 526-30. |
Western blot analysis of extracts from HUVEC and BAEC cells using VE-Cadherin (D87F2) XP® Rabbit mAb.使用VE-Cadherin (D87F2) 兔单抗对HUVEC和BAEC细胞提取物进行western blot分析。 | |
Immunoprecipitation of VE-caderin from HUVEC cells using VE-Cadherin (D87F2) XP® Rabbit mAb followed by western blot using the same antibody. Lane 1 is 5% input.使用VE-Cadherin (D87F2) 兔单抗对HUVEC细胞的VE-caderin进行免疫共沉淀实验，随后使用同样的抗体进行western blot分析。第一道为5%上样。 | |
Flow cytometric analysis of HeLa cells (blue) and HUVEC cells (green) using VE-Cadherin (D87F2) Rabbit mAb.使用VE-Cadherin (D87F2) 兔单抗对HeLa细胞（蓝色）和HUVEC细胞（绿色）进行流式细胞分析。 | |
Confocal immunofluorescent analysis of HUVE cells (left) and HeLa cells (right) using VE-Cadherin (D87F2) XP® Rabbit mAb (green). Actin filaments have been labeled with DY-554 phalloidin (red). Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye).使用VE-Cadherin (D87F2) 兔单抗对HUVE细胞（左）和HeLa细胞（右）进行激光共聚焦免疫荧光分析。肌动蛋白丝使用DY-554鬼笔环肽标记（红色）。蓝色假色=DRAQ5® #4084 （DNA荧光染料）。 |
