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- 详细信息
- 文献和实验
- 技术资料
- 库存:
999
- 供应商:
biorbyt
- 检测范围:
78.13-5000 pg/mL
- 检测方法:
Sandwich
- 适应物种:
Rat
- 样本:
serum, plasma, tissue homogenates, cell lysates and other biological fluids
- 灵敏度:
6.4 pg/mL
- 规格:
48 T
产品别名:Endocan
应用笔记:standard: 5000 pg/mL. Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat ESM1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ESM1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat ESM1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat ESM1 in the samples is then determined by comparing the OD of the samples to the standard curve
实验时长:3.5h
UniProt ID:P97682
Note:For research use only.
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文献和实验Derivation, Maintenance, and Characterization of Rat Embryonic Stem Cells In Vitro
describes the long-term cultivation of an alkaline phosphatase-positive rat embryonic stem cell-like line (RESC) and their differentiation into neuronal, endothelial, and hepatic lineages. The RESCs can be characterized by typical growth in single cells
To identify specific proteins expressed at the endothelial cell surface we used mass spectrometry, database searching and immuno-blotting, to analyse endothelial plasma membranes and caveolae isolated from rat tissues35, 36, as well as cultured rat lung
【资源】[共享]Adhesion Protein Protocols——(很有用的)
Materials 2.1— Construction of Adhesion Molecule—Ig Chimeras 2.2— Electroporation of Cells 2.3— Harvest and Culture of Transfectant Clones 2.4— Selection (ELISA) and Subcloning 2.5— Purification of Chimeric Proteins 3— Methods 3.1—







