Nahreini P, Woody M J, Zhou S Z, Srivastava A
Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis 46202-5120.
Gene. 1993 Feb 28;124(2):257-62. doi: 10.1016/0378-1119(93)90402-o.
We have constructed several plasmid vectors with which a more efficient molecular cloning, followed by rescue, replication, and packaging of DNA fragments, can be achieved. The availability of these vectors should facilitate construction of a variety of recombinant adeno-associated virus 2 (AAV)-based virions containing therapeutic genes for potential use in human gene therapy.
我们构建了几种质粒载体,利用这些载体可实现更高效的分子克隆,随后对DNA片段进行拯救、复制和包装。这些载体的可用性应有助于构建多种基于重组腺相关病毒2(AAV)的病毒粒子,这些病毒粒子含有可用于人类基因治疗的治疗性基因。