- ￥2980
- LSM Bio
- 78-5000pg/ml
- 39pg/ml
- 进口
- ELI-05724m
- 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：
20
- 供应商：
LSM BIO
- 检测范围：
78-5000pg/ml
- 检测方法：
夹心法ELISA或竞争法ELISA
- 应用：
检测小鼠血清，血浆，组织匀浆内的目标蛋白Cytochrome b561, Cyb561含量
- 适应物种：
小鼠
- 标记物：
Cytochrome b561, Cyb561
- 样本：
小鼠血清，血浆，组织匀浆及其他生物样本
- 灵敏度：
39pg/ml
- 规格：
96Tests
Mouse Cytochrome b561, Cyb561 ELISA试剂盒
Product Name: Mouse Cytochrome b561, Cyb561 ELISA试剂盒
Product Name: Mouse Cytochrome b561, Cyb561 ELISA试剂盒
Gene Name: Mouse Cytochrome b561, Cyb561
Detect Range:78-5000pg/ml
Sensitivity:39pg/ml
Target Protein Name: Mouse Cytochrome b561, Cyb561
Alternative Name: Mouse Cytochrome b561, Cyb561
ELISA type:Sandwich ELISA Kit
ELISA Test Principle:
NOTE:FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
Product Description: Mouse Cytochrome b561, Cyb561 ELISA试剂盒 allows for the in vitro quantitative determination of Mouse Cytochrome b561, Cyb561 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
The microtiter plate provided in Mouse Cytochrome b561, Cyb561 ELISA试剂盒 has been pre-coated with an Mouse Cytochrome b561, Cyb561 antibody specific to Mouse Cytochrome b561, Cyb561 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Cytochrome b561, Cyb561 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 Mouse Cytochrome b561, Cyb561 , 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 Mouse Cytochrome b561, Cyb561 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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