- ￥3480
- LSM Bio
- 0.78-50ng/ml
- 0.469ng/ml
- 进口
- ELI-47690b
- 2025年07月14日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
100
- 供应商：
LSM BIO
- 检测范围：
0.78-50ng/ml
- 检测方法：
夹心法
- 应用：
利用ELISA方法体外定量检测牛血清，血浆等样本中目标蛋白的浓度
- 适应物种：
牛
- 标记物：
Bovine Gap junction beta-2 protein,GJB2
- 样本：
牛的血浆，血清，细胞上清等
- 灵敏度：
0.469ng/ml
- 规格：
96tests
Bovine Gap junction beta- 2 protein, GJB2 ELISA KIT
Product Name:Bovine Gap junction beta- 2 protein, GJB2 ELISA KIT
Packing:96T
Catalog No.:ELI-47690b
Gene Name:Bovine Gap junction beta-2 protein, GJB2
Detect Range:0.313-20ng/ml
Sensitivity:0.188ng/ml
Target Protein Name:Bovine Gap junction beta-2 protein, GJB2
Alternative Name:GJB2,Bovine Gap junction beta-2 protein, GJB2
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Bovine Gap junction beta- 2 protein, GJB2 ELISA KIT allows for the in vitro quantitative determination of Bovine Gap junction beta-2 protein, GJB2 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Bovine Gap junction beta- 2 protein, GJB2 ELISA KIT has been pre-coated with an Bovine Gap junction beta-2 protein, GJB2 antibody specific to Bovine Gap junction beta-2 protein, GJB2 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Bovine Gap junction beta-2 protein, GJB2 and then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain Bovine Gap junction beta-2 protein, GJB2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm.The concentration of Bovine Gap junction beta-2 protein, GJB2 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
NOTE:FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
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文献和实验Evaluating Modulators of “Regulator of G‐protein Signaling” (RGS) Proteins
. Described in this unit are high?throughput screening procedures for identifying modulators of RGS protein?mediated GTPase acceleration (GAP activity), for assessment of RGS domain/G? interactions (most avid in vitro when G? is bound by aluminum tetrafluoride
Mapping Networks of Protein‐Mediated Physical Interactions Between Chromatin Elements
. However, these methods do not specifically identify the protein component(s) that might mediate such interactions. This unit provides a detailed protocol for Combined 3C?ChIP?Cloning (6C) technology, which combines multiple techniques to simultaneously identify physical
Comparative Protein Structure Modeling Using MODELLER
‐dependent gap penalties. J. Mol. Biol. 310:243‐257. Sibanda, B.L., Blundell, T.L., and Thornton, J.M. 1989. Conformation of beta‐hairpins in protein structures. A systematic
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