• GFP has also been used for more, um, creative purposes.

    绿色荧光蛋白还具有更富创造性的用途。

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  • In 1992 Dr Prasher also cloned GFP, so that it no longer had to be harvested from living creatures.

    在1992年,普拉舍博士也克隆了“绿色荧光蛋白”(gfp),所以它不再必须是从活着的生物体中提取。

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  • A tantalizing prospect because almost any organism, from a bacterium to a cow, can be programmed to synthesize GFP.

    这个前景是美好的,因为从细菌到牛都可以用来合成荧光蛋白质。

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  • This expanded the possibilities for exploiting bioluminescence dramatically, because it meant that GFP did not have to be injected into tissue.

    这样极大提高了开发生物荧光的可能性,因为这意味着“绿色荧光蛋白”不再必须被注射到组织中,取而代之的是,其基因序列可以被加入到活体的基因中去。

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  • In 2000, French scientists spliced GFP into a white rabbit's genome; Chicago artist Eduardo Kac claimed it was his idea, though scientists later disputed that.

    2000年,法国科学家将绿色荧光蛋白基因转接进兔子的基因组中;芝加哥的艺术家爱德华多·卡克(EduardoKac)宣称这是他的创意,不过后来科学家们反驳了他。

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  • GFP provides major journals and other sources related to business.

    巨灵财经资讯提供与商业有关的重要学术期刊及其他信息资料。

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  • Since GFP makes its own chromophore, it is perfect for genetic engineering.

    由于GFP可以自己生成荧光团,所以适用于基因工程。

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  • RESULTS the expression of GFP was obviously induced only in the curcumin group.

    结果姜黄素诱导了绿色荧光蛋白的表达。

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  • In this review, we mainly describe discovery, improvement, and application of GFP.

    本文主要回顾总结了绿色荧光蛋白的发现、优化改造及其应用。

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  • Objective To construct saccharomyces cerevisiae expression vector with GFP as report gene.

    目的构建以绿色荧光蛋白(GFP)为报告基因的酿酒酵母表达载体。

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  • Objective: To obtain GFP-RECK expression vector and to express it in glioma cell line SHG44.

    目的:获得RECK基因GFP融合蛋白表达载体并使其在脑胶质瘤细胞SHG44中表达。

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  • It is intended to provide an artificial mutant of GFP having a novel emission wavelength peak.

    本发明提供一种具有新的发光波长峰的GFP的人工突变体。

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  • The adipose cells were transfected with Ad-GFP at the different multiplicity of infection (MOI).

    以不同感染强度的携带绿色荧光蛋白基因重组腺病毒转染诱导后的脂肪细胞。

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  • Objective To find out the role of GFP-tag on the localization of overexpressed MDA-7/IL-24 protein.

    目的了解标签蛋白GFP的位置对过表达的MDA-7/IL-24融合蛋白亚细胞定位的影响。

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  • But wild type GFP and EGFP are not ideal to detect the transient changes of gene expression regulation.

    但野生型GFP及增强型GFP等因半衰期长,稳定性强,对反映一过性转录表达调控的变化不甚理想。

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  • The invention can employ GFP to realize quick online detection of thalli concentration and enzyme activity.

    本发明可以利用GFP蛋白实现菌体浓度和酶活的快速在线检测。

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  • The green fluorescence protein (GFP) gene recombinant virus labeling is a new method for the neuroanatomical studies.

    绿色荧光蛋白(GFP)基因重组病毒标记技术是神经解剖研究的新方法。

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  • Objective To establish a culture system for human embryonic stem cell and label the hES cells with GFP by lentivirus.

    目的稳定培养人胚胎干细胞,并通过慢病毒载体对其进行绿色荧光蛋白标记。

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  • Generally, GFP is attached at one end of the protein and does not significantly alter the attached protein's function.

    一般情况下,GFP是挂在该蛋白的一个末尾上,不会明显地改变该蛋白的功能。

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  • Results Saccharomyces cerevisiae expression vector with GFP as report gene was constructed and expressed successfully.

    结果成功构建了以GFP为报告基因的酿酒酵母载体,并在酵母中得到表达。

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  • In awarding the prize, the Royal Swedish Academy compared the impact of GFP on science to the invention of the microscope.

    宣布奖项时,瑞典皇家科学院称绿色荧光蛋白在科学领域的重要性堪比显微镜的发明。

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  • The article on the physical and chemical properties, the fluorescence characteristics, improvement and application of GFP are reviewed.

    我们就GFP的理化性质、荧光特性、改进和应用研究进行了综述。

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  • The result also professes that the MAR sequence can enhance the expression of GFP gene significantly (data was shown in another paper).

    研究还显示,MAR序列能明显增强绿色荧光蛋白基因的表达能力(这一结果在另文讨论)。

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  • They also observed that the fibers were fluorescent, indicating that the GFP molecules retained their 3-d structure while linked together.

    他们还观察到该纤维发荧光,这表明当GFP分子连接在一起时还保持其三维结构。

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  • Lentivirus with GFP reporter can infect differentiated adipocytes. The infection efficiency was about 80%, and infected cells were in good conditions.

    携带GF P报告基因的慢病毒可感染成熟脂肪细胞,感染率约为80%,且细胞被感染后状态良好。

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  • The atrazine-degrading genetically engineered microorganism(GEM) was labeled by transforming a plasmid containing green fluorescent protein(GFP) gene.

    通过转化绿色荧光蛋白基因质粒,对阿特拉津降解基因工程菌进行标记。

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  • Methods BTT-T739 cells, a mouse bladder transitional cell carcinoma cell line, were tranfected with GFP plasmid to screen stable GFP expressing clones.

    方法 将绿色荧光蛋白 (GFP)表达质粒导入 膀胱癌细胞株BTT T739,筛选出高表达GFP的细胞克隆并配置成细胞悬液。

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  • But there were no GFP expression in arabidopsis protoplast with the amine silane magnetic nanoparticles and the chitosan magnetic nanoparticles transformation.

    而氨基硅烷磁性纳米颗粒和壳聚糖磁性纳米颗粒转化拟南芥原生质体未见GFP的表达。

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  • But there were no GFP expression in arabidopsis protoplast with the amine silane magnetic nanoparticles and the chitosan magnetic nanoparticles transformation.

    而氨基硅烷磁性纳米颗粒和壳聚糖磁性纳米颗粒转化拟南芥原生质体未见GFP的表达。

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