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Enhanced electro-mediated gene delivery using carrier genes

机译:利用载体基因增强电介导的基因传递

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Low wtransfection and expression of target genes has been a problem in gene delivery for clinical therapy. In this study, we present a method for enhancing the transfection efficiency of target genes by electroporation using carrier genes. To evaluate the transfection efficiency, we transfected HeLa cells with luciferase genes (pGL3-control) and then measured the luciferase activity. In our experiments, the prokaryotic expression vector pCR2.1 was used as a carrier gene in the electro-mediated gene delivery. The result shows that the luciferase gene can be effectively transferred into the cell membrane with the aid of carrier genes. In the presence of carrier genes, luciferase activities increased two- to three-fold compared with that in the absence of carrier genes. We also investigated the effect of the weight ratio of luciferase genes to carrier genes on transfection efficiency and found no significant relationship between them. Consequently, we believe that carrier genes are potentially beneficial for promoting transfection and expression of target genes in biological applications.
机译:低wtransfection和目标基因的表达已成为临床治疗的基因传递中的问题。在这项研究中,我们提出了一种通过使用载体基因进行电穿孔来提高靶基因转染效率的方法。为了评估转染效率,我们用萤光素酶基因(pGL3-control)转染了HeLa细胞,然后测量了萤光素酶活性。在我们的实验中,原核表达载体pCR2.1被用作电介导的基因传递中的载体基因。结果表明,萤光素酶基因可以通过载体基因有效地转移到细胞膜中。在不存在载体基因的情况下,与不存在载体基因的情况相比,萤光素酶活性增加了2到3倍。我们还研究了萤光素酶基因与载体基因的重量比对转染效率的影响,发现它们之间没有显着关系。因此,我们认为载体基因在生物应用中对于促进靶基因的转染和表达具有潜在的益处。

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