Overview:
| Product Name | VE Cadherin Antibody | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | Rabbit Anti-Human VE Cadherin Polyclonal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species Reactivity | Human, Mouse | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Applications | WB | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Antibody Dilution | WB (1:2000); optimal dilutions for assays should be determined by the user. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Host Species | Rabbit | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Immunogen Species | Human | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Immunogen | A synthesized peptide derived from human VE-Cadherin | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Conjugates |
Alkaline Phosphatase, APC, ATTO 390, ATTO 488, ATTO 565, ATTO 594, ATTO 633, ATTO 655, ATTO 680, ATTO 700, Biotin, FITC, HRP, PE/ATTO 594, PerCP, RPE, Streptavidin, Unconjugated
StreptavidinProperties:
Streptavidin Datasheet Biotin | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| R-PE (R-Phycoerythrin) | ||
Overview:
R-PE Datasheet | ![]() | Optical Properties: λex = 565 nm λem = 575 nm εmax = 2.0×106 Φf = 0.84 Brightness = 1.68 x 103 Laser = 488 to 561 nm Filter set = TRITC |
Properties
| Storage Buffer | PBS pH 7.4, 50% glycerol, 150mM NaCl, 0.02% sodium azide |
| Storage Temperature | -20ºC |
| Shipping Temperature | Blue Ice or 4ºC |
| Purification | Affinity Purified |
| Clonality | Polyclonal |
| Isotype | IgG |
| Specificity | Detects endogenous levels of total VE-Cadherin |
| Cite This Product | StressMarq Biosciences Cat# SPC-1290, RRID: AB_2713025 |
| Certificate of Analysis | A 1:1000 dilution of SPC-1290 was sufficient for detection of VE Cadherin in 10 µg of Jurkat cell lysates by ECL immunoblot analysis using Goat Anti-Rabbit IgG:HRP as the secondary antibody. |
Biological Description
| Alternative Names | 7B4 Antibody, Cadherin 5 Antibody, Cadherin 5 type 2 Antibody, cadherin, vascular endothelial Antibody, CD 144 Antibody, CDH 5 Antibody, Endothelial specific cadherin Antibody, Vascular endothelial cadherin Antibody, VE Cad Antibody |
| Research Areas | Cancer, Cardiovascular Markers, Cardiovascular System, Cell adhesion, Cell Signaling, Cytoskeleton, Endothelial Cells, Invasion/microenvironment |
| Cellular Localization | Cell Junction, Cell membrane |
| Accession Number | NP_001786.2 |
| Gene ID | 1003 |
| Swiss Prot | P33151 |
| Scientific Background | Cadherins are a super family of transmembrane glycoproteins that contain cadherin repeats of ~ 100 residues in their extracellular domain. They mediate calcium-dependent cell-cell adhesion and play critical roles in normal tissue development. Specifically, VE Cadherin plays an inportant role in endothelial cell biology. It associates with alpha-catenin forming a link to the cytoskeleton. And its signaling, expression, and localization correlate with vascular permeability and tumor angiogenesis. |
| References |
1. Wheelock M.J. and Johnson K.R. (2003) Annu Rev Cell Dev Biol. 19: 207-235. 2. Rabascio C., et al. (2004) Cancer Res. 64: 4373-4377. 3. Yamaoka-Tojo M., et al. (2006) Arterioscler Thromb Vasc Biol. 26: 1991-1997. |
Product Images
Western blot analysis of Human Jurkat cell lysates showing detection of ~120kDa VE Cadherin protein using Rabbit Anti-VE Cadherin Polyclonal Antibody (SPC-1290). Lane 1: Human Jurkat Whole Cell lysates treated with the immunizing peptide. Lane 2: Human Jurkat Whole Cell lysates. Primary Antibody: Rabbit Anti-VE Cadherin Polyclonal Antibody (SPC-1290) at 1:1000. Predicted/Observed Size: ~120kDa.
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| ATTO 390 | ||
Overview:
ATTO 390 Datasheet | ![]() | Optical Properties: λex = 390 nm λem = 479 nm εmax = 2.4×104 Φf = 0.90 τfl = 5.0 ns Brightness = 21.6 Laser = 365 or 405 nm |
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② 应取pH8.0,这样可使核苷酸带较多负电荷,利于吸附于阴离子交换树脂柱。虽然pH 11.4时核苷酸带有更多的负电荷,但pH过高对分离不利。
③ 当不考虑树脂的非极性吸附时,根据核苷酸负电荷的多少来决定洗脱速度,则洗脱顺序为CMP>AMP> GMP > UMP,但实际上核苷酸和聚苯乙烯阴离子交换树脂之间存在着非极性吸附,嘌呤碱基的非极性吸附是嘧啶碱基的3倍。静电吸附与非极性吸附共同作用的结果使洗脱顺序为:CMP> AMP > UMP >GMP。
1. Buffer中离子浓度过大,甘氨酸或者Tris碱有可能疏忽多加了
2.没有加相应浓度的SDS
3.电泳周围温度高,也是一个原因















