- ￥2890
- LSM Bio
- 0.31-20NG/ML
- 0.1NG/ML
- 进口
- EF007320
- 2025年07月14日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
50
- 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 Pre-S1
- 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
Pre-S1 ELISA KIT|Human
Catalog EF007320
Packing 48T/96T
Reactivity Human
Detect Range Qualitative
Pre-S1 ELISA KIT Sensitivity< Qualitative
Application Pre-S1 ELISA KIT|Human is for detecting the concentration of Human Pre-S1 in serum, plasma, tissue homogenates and other biological fluids.
Storage condition 6 month at 4 Centigrade
Principle of Pre-S1 ELISA KIT|Human
The microtiter plate provided in Pre-S1 ELISA KIT|Human has been pre-coated with an Human Pre-S1 antibody specific to Human Pre-S1. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated Human Pre-S1antibody preparation specific for Human Pre-S1 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 Pre-S1, 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 Pre-S1in the samples is then determined by comparing the O.D. of the samples to the standard curve.
*Please noted that Pre-S1 ELISA KIT|Human is only for RUO (Research Use Only), Not for the diagnostic Purpose!
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文献和实验8°C. Discard the supernatant. 5) Resuspend the cells in 900 μl Buffer 1. 6) Add 100 μl pre-washed Depletion MyOne SA Dynabeads®. 7) Incubate for 15 min at 2–8°C with gentle tilting and rotation. 8)
RAT/MOUSE GROWTH HORMONE ELISA KIT
实验原理 This assay is a Sandwich ELISA based, sequentially, on: 1) capture of rat or mouse Growth Hormone molecules from samples to the wells of a microtiter plate coated by a pre-titered amount of anti-Growth Hormone
施一公团队再获新进展！解析人类 pre-tRNA 剪接机制，完善剪接体结构「地图」
长久以来，剪接体的调控机理是怎样的，它们在细胞内部的动态组合和变化是怎样的，深深地吸引着科学家们的研究兴趣，但其神秘的面纱一直未被揭开。 2023 年 4 月 6 日，西湖大学施一公团队在 Molecular Cell 杂志发表研究论文 Structural basis of pre-tRNA intron removal by human tRNA splicing endonuclease，该研究首次解析了人类 tRNA 剪接内切核酸酶（TSEN）在催化前和催化后状态下与全长 tRNA
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