- ￥2890
- LSM Bio
- 0.156-10ng/ml
- 0.078ng/ml
- 国产
- ELI-19284h
- 2026年03月16日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
20
- 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：
Lymphocyte transmembrane adapter 1,LAX1
- 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 Lymphocyte transmembrane adapter 1, LAX1 ELISA KIT
Product Name:Human Lymphocyte transmembrane adapter 1, LAX1 ELISA KIT
Packing:96T
Catalog No.:ELI-19284h
Gene Name:LAX1
Detect Range:0.156-10 ng/mL
Sensitivity:0.078ng/mL
Target Protein Name:Lymphocyte transmembrane adapter 1(LAX1
Alternative Name:LAX1,Lymphocyte transmembrane adapter 1(LAX1
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Human Lymphocyte transmembrane adapter 1, LAX1 ELISA KIT allows for the in vitro quantitative determination of Lymphocyte transmembrane adapter 1(LAX1 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Human Lymphocyte transmembrane adapter 1, LAX1 ELISA KIT has been pre-coated with an Lymphocyte transmembrane adapter 1(LAX1 antibody specific to Lymphocyte transmembrane adapter 1(LAX1 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Lymphocyte transmembrane adapter 1(LAX1 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 Lymphocyte transmembrane adapter 1(LAX1, 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 Lymphocyte transmembrane adapter 1(LAX1 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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