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- 文献和实验
- 技术资料
- 供应商:
武汉益普生物科有限公司
- 检测范围:
0.63-40 ng/mL
- 检测方法:
Sandwich
- 适应物种:
Human
- 样本:
serum, plasma, tissue homogenates, cell lysates and other biological fluids
- 灵敏度:
0.235 ng/mL
- 规格:
48T/96T
| 规格: | 48T | 产品价格: | ¥1820.0 |
|---|---|---|---|
| 规格: | 96T | 产品价格: | ¥2600.0 |
| 中文名称 | 人脂蛋白脂酶(LIPD)酶联免疫吸附检测试剂盒 |
| 英文名称 | Human LIPD(Lipase, Lipoprotein) ELISA Kit |
| 别名 | LPL; Lipoprotein Lipase |
| 货号 | ELK1459 |
| 反应种属 | Human |
| P06858 | P06858 |
| 检测类型 | Sandwich |
| 灵敏度 | 0.235 ng/mL |
| 标准品 | 40 ng/mL |
| 检测范围 | 0.63-40 ng/mL |
| 样本类型 | serum, plasma, tissue homogenates, cell lysates and other biological fluids |
| 反应时间 | 3.5h |
| 检测原理 | 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 LIPD. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LIPD. 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 LIPD, 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 LIPD in the samples is then determined by comparing the OD of the samples to the standard curve. |
| 研究领域 | Enzyme & Kinase;Metabolic pathway;Cardiovascular biology; |

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文献和实验【信息】Northstar BioProducts(NSBP)
/mg, ≥5 units/mL M.W.: ~70,000 (SDS-PAGE) 其它酶(Miscellaneous Enzymes)主要包括:Lipase(脂肪酶)、Protease(蛋白酶)、Esterase(酯酶)、Collagenase(胶原酶)、Enzymatic Deglycosylation Kit(酶糖基化试剂盒)、Oxidase(氧化酶)、Phospholipase(磷脂酶)、Thermolysin(嗜热菌蛋白酶)、Uricase(尿酸
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,8:81-89 [20]Simmons T,Newhous Y M, Arnold K S et al . Human low density lipoprotein receptor fragment successful refolding of a functionally active ligand-binding domain produced in E.coli.J Biol Chem,1997,272(41):25531-25536 [21]Rozema D,Gellman
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