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- 文献和实验
- 技术资料
- 供应商:
武汉研升生物科有限公司
- 检测范围:
0.32-20 ng/mL
- 检测方法:
Sandwich
- 适应物种:
Human
- 样本:
Tissue homogenates and other biological fluids.
- 灵敏度:
0.126 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 | 人亮氨酸丰富重复FLII相互作用蛋白1(LRRFIP1)酶联免疫吸附检测试剂盒 |
| 英文名称 | Human LRRFIP1(Leucine Rich Repeat In FLII Interacting Protein 1) ELISA Kit |
| 别名 | GCF2; FLAP-1; FLIIAP1; GCF-2; HUFI-1; TRIP; GC-Binding Factor 2; TAR RNA-interacting protein |
| 货号 | ELK4348 |
| 反应种属 | Human |
| Q32MZ4 | Q32MZ4 |
| 检测类型 | Sandwich |
| 灵敏度 | 0.126 ng/mL |
| 标准品 | 20 ng/mL |
| 检测范围 | 0.32-20 ng/mL |
| 样本类型 | Tissue homogenates 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 LRRFIP1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LRRFIP1. 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 LRRFIP1, 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 LRRFIP1 in the samples is then determined by comparing the OD of the samples to the standard curve. |
| 研究领域 | Immune molecule; |

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文献和实验Discovery and Characterization of Leucine-Rich Repeat-Containing G Protein-Coupled Receptors
Leucine-rich repeat-containing G protein-coupled receptors (LGRs) are type A rhodopsin-like GPCRs that include the glycoprotein pituitary hormone receptors for the thyroid-stimulating, follicle-stimulating, and luteinizing hormones (TSH, FSH
Measuring the Activity of Leucine-Rich Repeat Kinase 2: A Kinase Involved in Parkinsons Disease
Mutations in the LRRK2 (Leucine-Rich Repeat Kinase 2) gene are the most common cause of autosomal dominant Parkinson’s disease. LRRK2 has multiple functional domains including a kinase domain. The kinase activity of LRRK2 is implicated
PTEN-induced novel kinase 1 (PINK1) and leucine-rich repeat kinase 2 (LRRK2) are two protein kinases associated with recessive and dominant forms of parkinsonism, respectively. Mutations in PINK1 cause loss of protein function
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