- ￥2890
- LSM Bio
- 参照说明书
- 0.31-20ng/ml
- 国产
- ELI-09930h
- 2025年07月06日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
50
- 供应商：
LSMBIO
- 检测范围：
参照说明书
- 检测方法：
夹心法/竞争法
- 应用：
0.1ng/ml
- 适应物种：
人
- 标记物：
CXorf69 (Putative uncharacterized protein CXorf69) ELISA K
- 样本：
人血清、血浆或其它相关生物液体中天然和重组蛋白
- 灵敏度：
0.31-20ng/ml
- 规格：
96T
Human CXorf69 (Putative uncharacterized protein CXorf69) ELISA Kit (CUSTOM)
96 Tests
Operating instructions
FOR RESEARCH USE ONLY!
Alternative name
Human CXorf69 ELISA KIT ,Human SMIM10 ELISA KIT ,Human small integral membrane protein 10 ELISA KIT ,Human Putative uncharacterized protein CXorf69 ELISA KIT
Intended use
Human CXorf69 ELISA kit allows for the in vitro quantitative determination of Human Putative uncharacterized protein CXorf69 concentrations in serum, plasma, tissue homogenates, cell culture supernates, and other biological fluids.
Test principle
Human CXorf69 ELISA kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with an antibody specific to CXorf69, During the reaction, CXorf69 in the sample or standard competes with a fixed amount of biotin-labeled CXorf69 for sites on a pre-coated Monoclonal antibody specific to CXorf69. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. 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 ± 2 nm. The concentration of CXorf69 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Customized product Min.Order 5kits
Delivery time 4-6month
Order Human CXorf69 ELISA kit by email:
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ANTIBODY BINDING TO PROTEIN A AND PROTEIN G
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acid sequence of human 14-3-3 protein eta was highly homologous to that of previously reported bovine and rat 14-3-3 proteins with only two amino acid differences.The sequence carries structural features as putative regions responsible for activation
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