Results The positive GFP gene was about 30 % - 35 % in lens epithelial cells.

结果基因转染后可见晶状体上皮细胞的GFP表达率在30%～35%.

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Methods rVSMCs were transfected with an adenoviral vector expressing Mfn 2 ( Adv - Mfn 2 - GFP ).

方法体外培养rVSMCs, 感染含有Mfn2基因的腺病毒载体 ( Adv -Mfn2-GFP ).

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The NIH 3 T 3 infected rGFP - AAV expressed significantly GFP fluorescence, which showed that rGFP - AAV was infectious virions.

感染了重组 GFP -AAV的大鼠NIH3T3细胞表达了明显的GFP荧光.

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Both genes were cloned into GFP expression vector pIRES 2 EGFP and transfected into HeLa cells.

将上述基因克隆入绿色荧光蛋白(GFP)表达载体pIRES2-EGFP中,转染人HeLa细胞,在荧光显微镜和电镜下观察转染细胞的形态和结构.

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The localization assays showed that COX dispersed in whole transfected COS 7 cells.

随后构建了COX-GFP 融合表达载体,观察到COX在 COS_7细胞中为全细胞分布.

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Studies of the bioluminescent mechanisms of jellyfish to date have focused primarily one species , Aequorea victoria.

迄今所研究的GFP和 aequorin主要来源于维多利亚多管发光水母(Aequoreavictoria).

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