- ￥2890
- LSM Bio
- 0.156-10ng/ml
- 0.078ng/ml
- 国产
- ELI-19061h
- 2025年07月05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：
Taste receptor type 2 member 31,TAS2R31
- 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 Taste receptor type 2 member 31, TAS2R31 ELISA KIT
Product Name:Human Taste receptor type 2 member 31, TAS2R31 ELISA KIT
Packing:96T
Catalog No.:ELI-19061h
Gene Name:TAS2R31
Detect Range:78-5000 pg/mL
Sensitivity:32pg/mL
Target Protein Name:Taste receptor type 2 member 31(TAS2R31
Alternative Name:TAS2R31,Taste receptor type 2 member 31(TAS2R31
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Human Taste receptor type 2 member 31, TAS2R31 ELISA KIT allows for the in vitro quantitative determination of Taste receptor type 2 member 31(TAS2R31 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Human Taste receptor type 2 member 31, TAS2R31 ELISA KIT has been pre-coated with an Taste receptor type 2 member 31(TAS2R31 antibody specific to Taste receptor type 2 member 31(TAS2R31 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Taste receptor type 2 member 31(TAS2R31 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 Taste receptor type 2 member 31(TAS2R31, 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 Taste receptor type 2 member 31(TAS2R31 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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