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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:
0.16-10 ng/mL
- 检测方法:
Sandwich
- 适应物种:
Rat
- 样本:
Tissue homogenates and other biological fluids.
- 灵敏度:
0.057 ng/mL
- 规格:
48T/96T
| 规格: | 48T | 产品价格: | ¥1960.0 |
|---|---|---|---|
| 规格: | 96T | 产品价格: | ¥2800.0 |
| 中文名称 | 大鼠UDP葡萄糖醛酸转移酶2家族多肽B7(UGT2B7)酶联免疫吸附检测试剂盒 |
| 英文名称 | Rat UGT2B7(UDP Glucuronosyltransferase 2 Family, Polypeptide B7) ELISA Kit |
| 别名 | UGTB2B9; UDPGTh-2; 3,4-catechol estrogen-specific UDPGT |
| 货号 | ELK6958 |
| 反应种属 | Rat |
| Q62789 | Q62789 |
| 检测类型 | Sandwich |
| 灵敏度 | 0.057 ng/mL |
| 标准品 | 10 ng/mL |
| 检测范围 | 0.16-10 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 Rat UGT2B7. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat UGT2B7. 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 Rat UGT2B7, 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 Rat UGT2B7 in the samples is then determined by comparing the OD of the samples to the standard curve. |
| 研究领域 | Enzyme & Kinase; |

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文献和实验, or transcriptional activity of a promoter region. In this chapter, we describe a transient transfection assay for the functional characterization of naturally occurring variants of UDP-glucuronosyltransferase (UGT) 1A1. This phase II drug metabolizing enzyme
Transcriptional Regulation of UDP-Glucuronosyltransferases
the expression of UGT1A loci. This chapter presents an overview of the most recent developments in our understanding of transcriptional regulation of UDP-glucuronosyltransferase (UGT) genes, and specifically focuses on the regulation of UGTs via NRs
Glucuronidation of Fatty Acids and Prostaglandins by Human UDP-Glucuronosyltransferases
glucuronidation from both human liver micro-somes and human recombinant UDP-glucuronosyltransferase 2B7 (UGT2B7) are presented. Several unique methods for synthesis of FAs that are not commercially available are also described. Moreover, comprehensive methods
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