品牌咨询
联系方式
公司地址
苏州工业园区生物纳米园A4#216
联系电话
4000-520-616 / 18915418616
传真号码
0512-67156496
电子邮箱
info@ebiomall.com
公司网址
https://www.ebiomall.com

ECM BIOSCIENCES/VE-Cadherin (Extracellular region) Antibody/100 μl/CM0351

价格
¥5900.00
货号:CM0351
浏览量:127
品牌:ECM BIOSCIENCES
服务
全国联保
正品保证
正规发票
签订合同
商品描述

Cadherins are transmembrane glycoproteins vital in calcium-dependent cell-cell adhesion during tissue differentiation. Cadherins cluster to form foci of homophilic binding units. A key determinant to the strength of the cadherin-mediated adhesion may be by the juxtamembrane region in cadherins. VE-cadherin (Cadherin 5) is the major cadherin found in endothelial cells and has important roles during angiogenesis and maintenance of barrier permeability. The cytoplasmic domain of VE-cadherin comprises the juxtamembrane domain that binds to the p120 catenin, and the carboxylterminal domain that interacts with β- or γ-catenins. Modulation of tyrosine phosphorylation on one or more of the nine tyrosine sites in the cytoplasmic domain may be important for regulating both angiogenesis and permeability. Phosphorylation of Tyr-658 and Tyr-731 alters catenin binding, restores cell migration, and decreases barrier permeability. While VEGF-induced phosphorylation of Tyr-685 occurs through c-Src, and regulates endothelial cell migration, but not permeability.

 

References

Wallez Y. et al. (2007) Oncogene 26:1067. Baumeister U. et al. (2005) EMBOJ 24:1686.Potter M.D. et al. (2005) J Biol. Chem. 280(36):31906.

Western blot image of human umbilical vein endothelial cells stimulated with pervanadate (1 mM) for 30 min. then the blots were untreated (lanes 1 & 3) or treated with alkaline phosphatase (lanes 2 & 4). The blots were probed with rabbit polyclonal anti-VE-cadherin (Tyr-685) (lanes 1 & 2) or mouse monoclonal anti-VE-cadherin (lanes 3 & 4).

Immunocytochemical labeling of VE-Cadherin in aldehyde fixed andNP-40 permeabilized human NCI-H446 lung carcinoma cells. Thecells were labeled with mouse monoclonal anti-VE-Cadherin(CM0351). The antibody was detected using goat anti-mouseDyLight® 594.

Clone M035 was generated from a recombinant protein that included amino acids in the extracellular region of human VE-Cadherin. This sequence is not conserved in other cadherin family members.
*For more information, see UniProt Accession P33151
Mouse monoclonal antibody purified with protein A chromatography is supplied in 100µl phosphate-buffered saline, 50% glycerol, 1 mg/ml BSA, and 0.05% sodium azide. Store at –20°C. Stable for 1 year.

The products are are safely shipped at ambient temperature for both domestic and international shipments. Each product is guaranteed to match the specifications as indicated on the corresponding technical data sheet. Please store at -20C upon arrival for long term storage.

Clone M035 detects a 140 kDa* band corresponding to VE-cadherin in western blots of human endothelial cells. The antibody is recommended for use in western blot, ELISA and immunocytochemsitry, as well as for function blocking VE-cadherin homotypic adhesion.

*All molecular weights (MW) are confirmed by comparison to Bio-Rad Rainbow Markers and to western blotmobilities of known proteins with similar MW.

This kit contains:

KIT SUMMARY

ECM BIOSCIENCES的A431细胞裂解液A431细胞在细胞表面表达约106种表皮生长因子(EGF)受体。在用EGF刺激后,A431细胞的EGF受体磷酸化水平显着增加,随后激活了主要的细胞信号传导途径,例如PKB / Akt和MAP激酶途径。在EGF刺激后的不同时间点,这些细胞信号通路的下游,各种细胞骨架,细胞质和核蛋白被磷酸化。在含有10%胎牛血清的DMEM中生长的A431细胞的融合培养物在1%SDS,1.0 mM原钒酸钠,10 mM Tris(pH 7.4)缓冲液中裂解。在稀释至最终浓度和缓冲液之前,使用BCA方法(Pierce)确定蛋白质浓度。