- ￥2890
- LSM Bio
- 0.31-20NG/ML
- 0.1NG/ML
- 进口
- EF005756
- 2025年07月13日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
100
- 供应商：
LSMBIO
- 检测范围：
0.31-20NG/ML
- 检测方法：
夹心法
- 应用：
夹心法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 TH
- 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：
0.1NG/ML
- 规格：
96T
TH ELISA KIT|Human
Catalog EF005756
Packing 48T/96T
Reactivity Human
Detect Range 0.313-20ng/ml
TH ELISA KIT Sensitivity< 0.188ng/ml
Application TH ELISA KIT|Human is for detecting the concentration of Human TH in serum, plasma, tissue homogenates and other biological fluids.
Storage condition 6 month at 4 Centigrade
Principle of TH ELISA KIT|Human
The microtiter plate provided in TH ELISA KIT|Human has been pre-coated with an Human TH antibody specific to Human TH. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated Human THantibody preparation specific for Human TH 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 Human TH, 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 Human THin the samples is then determined by comparing the O.D. of the samples to the standard curve.
*Please noted that TH ELISA KIT|Human is only for RUO (Research Use Only), Not for the diagnostic Purpose!
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文献和实验人 TH17 酶联免疫 分析（ ELISA ） 试剂 盒使用说明书 本试剂仅供研究使用 目的：本试剂盒用于测定人血清，血浆及相关液体样本中辅助信息细胞的 TH17 含量。 实验原理 ： 本试剂盒应用 双抗体 夹心法测定 标本 中 人 TH17 水平。用纯化的 人 TH17 抗体 包被微孔板，制成固相 抗 体，往包被 单抗 的微孔中依次加入 TH17 ，再与HRP 标记的 TH17 抗体结合，形成抗体- 抗原 - 酶标
Warnings And Limitations This product is for research use only. Not intended for any animal or human therapeutic or diagnostic use unless otherwise stated. Follow appropriate laboratory guidelines. This product contains 0.02% sodium azide
Generation of Stable Th1/CTL-, Th2-, and Th17-Inducing Human Dendritic Cells
for testing the cytokine-producing abilities of these cells and their effectiveness in inducing Th1, Th2, and Th17 responses of CD4+ T cells and CTL responses of na�ve and memory CD8+ T cells.
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