- ￥3480
- LSM Bio
- 0.78-50ng/ml
- 0.469ng/ml
- 进口
- ELI-45917b
- 2025年07月15日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
100
- 供应商：
LSM BIO
- 检测范围：
0.78-50ng/ml
- 检测方法：
夹心法
- 应用：
利用ELISA方法体外定量检测牛血清，血浆等样本中目标蛋白的浓度
- 适应物种：
牛
- 标记物：
Bovine Phosphoglycerate mutase 1,PGAM1
- 样本：
牛的血浆，血清，细胞上清等
- 灵敏度：
0.469ng/ml
- 规格：
96tests
Bovine Phosphoglycerate mutase 1, PGAM1 ELISA KIT
Product Name:Bovine Phosphoglycerate mutase 1, PGAM1 ELISA KIT
Packing:96T
Catalog No.:ELI-45917b
Gene Name:Bovine Phosphoglycerate mutase 1, PGAM1
Detect Range:0.781-50ng/ml
Sensitivity:0.469ng/ml
Target Protein Name:Bovine Phosphoglycerate mutase 1, PGAM1
Alternative Name:PGAM1,Bovine Phosphoglycerate mutase 1, PGAM1
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Bovine Phosphoglycerate mutase 1, PGAM1 ELISA KIT allows for the in vitro quantitative determination of Bovine Phosphoglycerate mutase 1, PGAM1 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Bovine Phosphoglycerate mutase 1, PGAM1 ELISA KIT has been pre-coated with an Bovine Phosphoglycerate mutase 1, PGAM1 antibody specific to Bovine Phosphoglycerate mutase 1, PGAM1 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Bovine Phosphoglycerate mutase 1, PGAM1 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 Bovine Phosphoglycerate mutase 1, PGAM1, 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 Bovine Phosphoglycerate mutase 1, PGAM1 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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