重组DNA
质粒
生物
同源重组
病毒学
转染
基因
分子生物学
遗传学
作者
Jinyong Luo,Zhong-Liang Deng,Xiaoji Luo,Ni Tang,Wen-Xin Song,Jin Chen,Katie A. Sharff,Hue H. Luu,Rex C. Haydon,Kenneth W. Kinzler,Bert Vogelstein,Tong‐Chuan He
出处
期刊:Nature Protocols
[Springer Nature]
日期:2007-05-01
卷期号:2 (5): 1236-1247
被引量:798
标识
DOI:10.1038/nprot.2007.135
摘要
Recombinant adenoviruses provide a versatile system for gene expression studies and therapeutic applications. We have developed an approach that simplifies the generation and production of such viruses called the AdEasy system. A recombinant adenoviral plasmid is generated with a minimum of enzymatic manipulations, employing homologous recombination in bacteria rather than in eukaryotic cells. After transfection of such plasmids into a mammalian packaging cell line, viral production is conveniently followed with the aid of GFP encoded by a gene incorporated into the viral backbone. This system has expedited the process of generating and testing recombinant adenoviruses for a variety of purposes. In this protocol, we describe the practical aspects of using the AdEasy system for generating recombinant adenoviruses. The full protocol usually takes 4-5 weeks to complete.
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