随后人GRP94启动子克隆了荧光素酶基因上游区且缺氧环境中活性增强。
The human GRP94 promoter was then cloned upstream of the luciferase gene and showed enhanced activity in hypoxic conditions.
通过双荧光素酶报告基因测定法测定了 IGFBP-3 对由三碘甲状腺素刺激的生长激素启动子活性的影响。
The effect of IGFBP-3 on the growth hormone promoter activity stimulated by triiodothyronine was determined by dual-luciferase reporter assay.
研究者用基因工程的大肠埃希菌细胞生产荧光素酶作为AHL浓度函数。
The investigators used genetically engineered E. coli cells to produce luciferase as a function of AHL concentration.
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