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- prokaryotic luciferase 原核生物虫萤光素酶
- Sex may also be derived from prokaryotic processes. 性别也可能是源于原核进程。
- Addition of N protein in RRL system decreased luciferase activity. 在体外翻译体系中加入N蛋白,体外翻译被抑制。
- Luciferase activities were measured 72 hr post-transfection. 转染72小时后测量荧光素酶的活性。
- All living cells can be classified as prokaryotic or eukaryotic. 所有活细胞可以被划分为原核和真核两类。
- They appear to have a mixture of prokaryotic and eukaryotic genes. 它们被认为是某些真核生物基因和原核生物基因的混合体。
- Thus we constructed reporter vectors in which the reporter gene is luciferase. 经酶切鉴定以及测序分析确定载体构建正确。
- Objective:To clone,prokaryotic express and purify APOBEC3G protein in vitro. 目的:原核表达重组APOBEC3G蛋白,为其功能及免疫原性研究奠定基础。
- The transcriptional activation activity of GR was evaluated through method of relative activity of luciferase. 相对荧光素酶活性法检测gr转录激活功能的变化。
- SuperLight Luciferase Reporter Gene Assays for gene regulation and modulator screen. 荧光素酶报告基因检测试剂盒,用于基因调控筛查的。
- Plasmids are exta-chromosomal doublestranded, circular DNA molecules found in prokaryotic and eukaryotic cells. 质粒是在原核和真核细胞中发现的染色体外的双链环状DNA分子。
- EWS-FLI-1 can regulate the expression of luciferase because of its powerful transcription activity. 尤文肉瘤特异性的EWS-FLI-1融合蛋白有强烈的转录活性，可以促进虫荧光素酶基因高表达。
- Luciferase can be used in blood banks to determine if red blood cells are starting to break down. 例如，荧光素酶可以被用于检测血库中所存血液中的红血球是否开始破裂。
- The details of cloning, expression and function of biotinylated luciferase will be discussed in this paper. 本文将就生物素化荧光素酶的克隆、表达以及功能检测进行具体讨论。
- Studies on Prokaryotic Expression of Plant Anti-freeze and Salt Tolerance Genes. 盐基因原核表达研究。
- The fact that PTC124 binds to luciferase, he says, "has nothing to do with whether it's a good drug. 他认为，事实上PTC124连接上荧光素酶后，“并任何迹象显示出它是一种好药。”
- There was still some hope for anyone who wished to uphold the simple, prokaryotic picture of unsplit genes. 对于那些希望坚持基因都象原核生物那样不可分裂的简单理论的人来说，仍然存在着一线希望。
- Gentamicin and paromomycin increased luciferase activity up to 2.5- and 10-fold, respectively. 抑制的作用机制很可能和通读的增强有关，但此假设还需要进一步验证。
- However, as in the case of gentamicin, no increase in luciferase activity was observed in E. coli/pLux4 (UGA). 但与庆大霉素的研究结果相同，大肠杆菌/pLux4(UGA)的荧光素酶活性没有增加。
- The cDNA was subcloned into prokaryotic expression vector pET3d and overexpressed in E. coli BL21(DE3). 将该cDNA插入原核表达载体pET3d并在大肠杆菌BL21(DE3)中过量表达。
