Mizuguchi H, Kay M A
Division of Biological Chemistry and Biologicals, National Institute of Health Sciences, Tokyo, Japan.
Hum Gene Ther. 1999 Aug 10;10(12):2013-7. doi: 10.1089/10430349950017374.
We previously developed a two-plasmid in vitro ligation method that did not require a recombination step to produce new recombinant E1- or E1/E3-deleted adenoviral vectors. In this study, we have modified the system to improve the simplicity of vector construction and, in addition, to allow for production of an E1/E4-deleted vector.
我们之前开发了一种双质粒体外连接方法,该方法无需重组步骤即可产生新的缺失E1或E1/E3的重组腺病毒载体。在本研究中,我们对该系统进行了改进,以提高载体构建的简便性,此外,还可用于生产缺失E1/E4的载体。