- ￥2890
- LSM Bio
- 0.156-10ng/ml
- 0.078ng/ml
- 国产
- ELI-30714h
- 2025年07月12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：
0.156-10ng/ml
- 检测方法：
夹心法/竞争法
- 应用：
夹心法/竞争法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：
Human Metabotropic glutamate receptor 4,GRM4
- 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
Human Metabotropic glutamate receptor 4, GRM4 ELISA KIT
Product Name:Human Metabotropic glutamate receptor 4, GRM4 ELISA KIT
Packing:96T
Catalog No.:ELI-30714h
Gene Name:GRM4
Detect Range:78-5000 pg/mL
Sensitivity:32pg/mL
Target Protein Name:Metabotropic glutamate receptor 4(GRM4
Alternative Name:GRM4,Metabotropic glutamate receptor 4(GRM4
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Human Metabotropic glutamate receptor 4, GRM4 ELISA KIT allows for the in vitro quantitative determination of Metabotropic glutamate receptor 4(GRM4 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Human Metabotropic glutamate receptor 4, GRM4 ELISA KIT has been pre-coated with an Metabotropic glutamate receptor 4(GRM4 antibody specific to Metabotropic glutamate receptor 4(GRM4 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Metabotropic glutamate receptor 4(GRM4 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 Metabotropic glutamate receptor 4(GRM4, 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 Metabotropic glutamate receptor 4(GRM4 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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