- ￥2890
- LSM Bio
- 0.156-10ng/ml
- 0.078ng/ml
- 国产(香港)
- ELI-29197h
- 2026年04月29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：
Human Testin,TES
- 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 Testin, TES ELISA Kit
FOR RESEARCH USE ONLY!
96 Tests
Alternative name
Human TES ELISA KIT ,Human Testin ELISA KIT ,Human TESS ELISA KIT ,Human TESS-2 ELISA KIT ,Human testis derived transcript (3 LIM domains) ELISA KIT ,Human testin LIM domain protein ELISA KIT
Intended use
Human TES ELISA kit allows for the in vitro quantitative determination of Human Testin concentrations in serum, plasma, tissue homogenates, cell culture supernates, and other biological fluids.
Test principle
Human TES ELISA kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with an antibody specific to TES, During the reaction, TES in the sample or standard competes with a fixed amount of biotin-labeled TES for sites on a pre-coated Monoclonal antibody specific to TES. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. 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 ± 2 nm. The concentration of TES in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Range 0.62-40ng/ml
Human TES ELISA kit manual download
Order Human TES ELISA kit by email:
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文献和实验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
RAT/MOUSE GROWTH HORMONE ELISA KIT
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the presence or absence of the target substances in doping control specimens. Simulating human metabolic reactions using liver microsomal preparations, minute amounts of possible urinary metabolites were obtained that were characterized
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