- ￥2890
- LSM Bio
- 0.15-10NG/ML
- 0.078NG/ML
- 国产
- EF003803
- 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：
0.15-10NG/ML
- 检测方法：
夹心法
- 应用：
夹心法ELISA体外定量检测人血清、血浆或其它相关生物液体中蛋白浓度
- 适应物种：
人
- 标记物：
Trappc9/NIBP ELISA KIT
- 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：
0.078NG/ML
- 规格：
96T
Trappc9/NIBP ELISA KIT|Human
Catalog EF003803
Packing 48T/96T
Reactivity Human
Detect Range 0.156-10ng/ml
Trappc9/NIBP ELISA KIT Sensitivity< 0.094ng/ml
Application Trappc9/NIBP ELISA KIT|Human is for detecting the concentration of Human Trappc9/NIBP in serum, plasma, tissue homogenates and other biological fluids.
Storage condition 6 month at 4 Centigrade
Principle of Trappc9/NIBP ELISA KIT|Human
The microtiter plate provided in Trappc9/NIBP ELISA KIT|Human has been pre-coated with an Human Trappc9/NIBP antibody specific to Human Trappc9/NIBP. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated Human Trappc9/NIBPantibody preparation specific for Human Trappc9/NIBP 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 Human Trappc9/NIBP, 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 Human Trappc9/NIBPin the samples is then determined by comparing the O.D. of the samples to the standard curve.
*Please noted that Trappc9/NIBP ELISA KIT|Human is only for RUO (Research Use Only), Not for the diagnostic Purpose!
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文献和实验volume of 35 ml at room temperature. 2) Add the diluted buffy coat on top of 15 ml of Lymphoprep. 3) Centrifuge at 160 x g for 20 minutes at 20°C. Allow to decellerate without brakes. 4) Remove 20 ml of supernatant
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实验原理 This assay is a Sandwich ELISA based, sequentially, on: 1) capture of rat or mouse Growth Hormone molecules from samples to the wells of a microtiter plate coated by a pre-titered amount of anti-Growth Hormone
Isolation of c-Kit+ Human Amniotic Fluid Stem Cells from Second Trimester
to obtain c-Kit+ human AFS cells, starting from second trimester amniocentesis samples.
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