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- 详细信息
- 文献和实验
- 技术资料
- 库存:
999
- 供应商:
biorbyt
- 检测范围:
0.79-50 ng/mL
- 检测方法:
Sandwich
- 适应物种:
Bovine
- 样本:
Serum, plasma, tissue homogenates and other biological fluids
- 灵敏度:
0.27 ng/mL
- 规格:
48 T
产品别名:LPL
应用笔记:standard: 50 ng/mL. Test principle: 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 Cattle LPL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Cattle LPL. 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 Cattle LPL, 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 Cattle LPL in the samples is then determined by comparing the OD of the samples to the standard curve
实验时长:3.5h
UniProt ID:P11151
Note:For research use only.
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文献和实验Detecting Ligands Interacting with Lipoprotein Lipase
The primary role for lipoprotein lipase (LPL) is hydrolysis of triglycerides in chylomicrons and very low density lipoproteins (VLDL). This enzyme has also been implicated in the process of atherogenesis (for reviews see refs
In Vitro Transcription and Translation of Lipoprotein Lipase
LPL is regulated post-transcriptionally in response to several hormones. Post-translational regulation occurs in response to feeding (1 ,2 ). Glycosylation of LPL at the first N-linked glycosylation site is essential for catalytic activity
Determining Lipoprotein Lipase and Hepatic Lipase Activity Using Radiolabeled Substrates
Hepatic lipase (HL) and lipoprotein lipase (LPL) are two lipolytic enzymes that play an important role in the metabolism of circulating lipoproteins. Both enzymes catalyze the esterolysis of fatty acids present at the sn -1 (3) position







