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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 Ribonuclease H2 subunit A,RNASEH2A
- 样本:
牛的血浆,血清,细胞上清等
- 灵敏度:
0.469ng/ml
- 规格:
96tests
Bovine Ribonuclease H2 subunit A, RNASEH2A ELISA KIT
Product Name:Bovine Ribonuclease H2 subunit A, RNASEH2A ELISA KIT
Packing:96T
Catalog No.:ELI-44972b
Gene Name:Bovine Ribonuclease H2 subunit A, RNASEH2A
Detect Range:31.2-2000pg/ml
Sensitivity:18.75pg/ml
Target Protein Name:Bovine Ribonuclease H2 subunit A, RNASEH2A
Alternative Name:RNASEH2A,Bovine Ribonuclease H2 subunit A, RNASEH2A
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Bovine Ribonuclease H2 subunit A, RNASEH2A ELISA KIT allows for the in vitro quantitative determination of Bovine Ribonuclease H2 subunit A, RNASEH2A concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Bovine Ribonuclease H2 subunit A, RNASEH2A ELISA KIT has been pre-coated with an Bovine Ribonuclease H2 subunit A, RNASEH2A antibody specific to Bovine Ribonuclease H2 subunit A, RNASEH2A .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Bovine Ribonuclease H2 subunit A, RNASEH2A 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 Ribonuclease H2 subunit A, RNASEH2A, 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 Ribonuclease H2 subunit A, RNASEH2A 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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