- ￥5720
- biorbyt
- 4 μmol/L - 400 μmol/L
- orb390770
- 英国
- 2026年01月21日
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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：
4 μmol/L - 400 μmol/L
- 检测方法：
Detection
- 应用：
FA
- 适应物种：
All
- 样本：
Tissue extracts, Cell lysate
- 规格：
100 assay
产品别名：EC 1.4.1.13; Glutamate synthase; Glutamate (reduced nicotinamide adenine dinucleotide phosphate) synthase; Glutamate synthetase (NADP); Glutamine amide-2-oxoglutarate aminotransferase (oxidoreductase, NADP); Glutamine-ketoglutaric aminotransferase; GOGAT; L-glutamate synthase; L-glutamate synthetase; L-glutamine:2-oxoglutarate aminotransferase; NADPH-dependent glutamate synthase; NADPH-glutamate synthase
保存说明:Shipped and store at 4°C for 6 months.
Note：For research use only.
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文献和实验bodies inEscherichia coli . The current work describes a colorimetric assay for measuring RFAP synthase activity, and two modified procedures for expressing recombinant RFAP synthase genes to produce soluble, active enzyme. By lowering the incubation
Using N,N,N,N-tetramethyl-p-phenylenediamine (TMPD) to Assay Cyclooxygenase Activity In Vitro
activity. Colorimetric assays are often the preferred methods of enzyme analysis since they may be readily adapted to simple microplate formats that require relatively inexpensive and widely available instrumentation. The use of N ,N ,N �,N �-tetramethyl-p
-galactosidase gene (Adβgal) or the eNOS gene (AdeNOS) were infected into the NTS. In the Adβgal-infected rats, the local expression of β-galactosidase was confirmed by X-Gal staining, and β-galactosidase activity was quantified using a colorimetric assay
