质粒
转染
转基因
生物
效价
基因传递
载体(分子生物学)
HEK 293细胞
基因组
体外
病毒载体
基因转移
慢病毒
遗传增强
基因
计算生物学
病毒
重组DNA
细胞生物学
病毒学
遗传学
病毒性疾病
作者
Matthew J. Benskey,Fredric P. Manfredsson
出处
期刊:Methods in molecular biology
日期:2015-11-26
卷期号:: 107-114
被引量:48
标识
DOI:10.1007/978-1-4939-3271-9_8
摘要
Lentiviral (LV) vectors offer unique advantages over other gene delivery systems, namely the ability to integrate transgenes into the genome of both dividing and nondividing cells. Detailed herein is a simple protocol for the production LV vectors, describing the triple transfection of an LV transfer vector and LV helper plasmids into HEK-293 cells, and the subsequent purification of virions from the cellular media. The current protocol is versatile, and can be easily modified to fit the specific needs of the researcher in order to produce relatively high-titer LV vectors which can be used to transduce a wide variety of cells both in vitro and in vivo.
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