luciferase

Methods The method of luciferase reporter gene was used .

方法采用荧光素酶报告基因方法。

Primary Study on Rapid Bioluminescence Evaluation of Disinfection Effect Using Luciferase

荧光素酶生物发光法快速评价消毒效果的初步研究

The species , structure and applications of luciferase were researched .

文章就荧光素酶的种类、结构及应用进行了研究。

Methods : Cell culture , transient transfection and luciferase assay .

方法：细胞培养，瞬时转染和报告基因检测。

So it is necessary to carry out the study on improving the luciferase stability .

因此，开展对提高荧光素酶稳定性方法的研究很有必要。

The activity of luciferase was detected using dual luciferase reporter system .

通过双荧光素酶报告系统检测荧光素酶的活性。

Construction and identification of human Puma promotor luciferase report gene vector

人Puma启动子荧光素酶报告基因的构建和鉴定

The Species , Structure and Applications of Luciferase

荧光素酶的分类、结构与应用

We addressed this question with the method of luciferase reporter gene .

我们用荧光素酶报告基因的方法，探讨了这个问题。

Advances in Research on Luciferase in Biology and Medicine

荧光素酶在生物医学中的研究进展

Methods Luciferase reporter assay was used to detect the activity of promoter .

方法采用表达luciferase的报告基因载体检测启动子的活性。

We further studied the function of this fragment with luciferase report assay .

我们用luciferase报告基因的方法进一步研究了这个片段的功能。

Study on the Trehalose Protection on Activity of Luciferase

海藻糖对虫荧光素酶活性保护作用研究

Tet on gene expression system achieves quantitative control of luciferase gene expression in CHO cells

Tet-On基因表达系统定量调节荧光素酶基因在CHO细胞中的表达

Effects of Translation Initiation Region Secondary Structure on Expression of Luciferase Gene in COS-7 Cells

翻译起始区二级结构对荧光素酶基因在COS-7细胞中表达效率的影响

Reporter gene expression was detect by Luciferase . 3 .

用Luciferase法检测报告基因表达。

Application of Luciferase Report Gene in Transgenic Silkworm

荧光素酶报告基因在转基因蚕中的应用

To confirm this hypothesis , we used dual luciferase reporter gene assay .

为了支持这一观点，我们用双荧光素酶报告基因分析的方法进行验证。

IL-8 gene promoter activation was detected using dual luciferase reporter gene assay .

用双荧光素酶报告基因检测IL-8激活程度。

Construction of recombinant plasmid highly expressing luciferase in Drosophila S2 cells

果蝇S2细胞中高表达荧光素酶重组质粒的构建及活性测定

Secondly , we used the dual luciferase reporter gene assay system to confirm the target gene .

其次，采用双荧光素酶报告基因检测系统进行靶基因的确认。

The results show that the activity of luciferase is the highest 36 hours after transfection .

细胞实验的结果表明，Bm－N细胞转染36小时，荧光素酶基因的表达已达最高峰；

Establishment of cell model expressing HCV-C and luciferase fusion protein by microinjection

显微注射法建立含荧光素酶和HCV-C基因细胞模型

Promoter activity of eNOS gene was determined by luciferase reporter gene assay .

采用瞬时转染的方法，通过荧光素酶报告基因实验检测eNOS基因转录起始点上游长16kb启动子区域的活性。

Transcriptional activity of NF - κ B was determined using luciferase reporter gene assay .

应用荧光素酶报告基因技术检测DHMEQ对NF-κB基因活性的影响；

Construction of a luciferase reporter vector with resistance of neomycin

带新霉素抗性的萤光素酶报告载体的构建

Subsequently , the p21 promoter activity was detected using the luciferase reporter gene assay system .

利用荧光素酶报道基因表达系统，观察β1族整合蛋白过表达对p21启动子区的活性调节。

Construction of Recombinant Retroviral Vector Containing Firefly Luciferase Reporter Gene

萤火虫荧光素酶报告基因重组逆转录病毒载体的构建及鉴定

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。

Construction of BIV - ltr promoter expression system with firefly luciferase gene

萤火虫萤光素酶基因构建BIV－LTR启动子表达研究体系