- ￥2816 - 3784
- Biorbyt
- 0.32-20 ng/mL
- orb1817314
- 英国
- 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：
99
- 供应商：
Biorbyt
- 检测范围：
0.32-20 ng/mL
- 应用：
详询
- 适应物种：
Human
- 样本：
Tissue homogenates and other biological fluids.
- 规格：
96T/48T
| 规格： | 96T | 产品价格： | ￥3784.0 |
|---|---|---|---|
| 规格： | 48T | 产品价格： | ￥2816.0 |
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human FATP1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human FATP1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human FATP1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human FATP1 in the samples is then determined by comparing the OD of the samples to the standard curve.
产品名：Human FATP1(Fatty Acid Transport Protein 1) ELISA Kit
货号：orb1817314
产品中文名：Human FATP1(Fatty Acid Transport Protein 1) ELISA Kit 酶联免疫试剂盒
产品详情链接：https://www.biorbyt.com/human-fatp1fatty-acid-transpo-orb1817314.html
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文献和实验Synchronizing Protein Transport in the Secretory Pathway
?intersecting and non?intersecting pathways exist in cells to carry out proper transport, modification, and addressing. To analyze and visualize the intracellular trafficking of any secretory protein, we developed the retention using selective hooks (RUSH
Human Xanthine Oxidoreductase Determination by a Competitive ELISA
Xanthine oxidoreductase (XO) catalyses the oxidation of hypoxanthine to xanthine and of the latter to uric acid. The enzyme is present in traces in most of human tissues, including plasma, being more abundant in milk, liver, and intestine (1).
technical steps to recover uPA and PAI-1 protein from archived breast cancer tissues and to quantitatively determine uPA and PAI-1 protein content in tumor tissue extracts by enzyme-linked immunosorbent assay (ELISA) are described in detail. The technical
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