哼
基因转移
计算生物学
遗传增强
病毒载体
生物
基因传递
标准化
计算机科学
基因
遗传学
重组DNA
艺术
艺术史
表演艺术
操作系统
作者
Patrick Salmon,Didier Trono
标识
DOI:10.1002/0471142905.hg1210s54
摘要
Lentiviral vectors have emerged over the last decade as powerful, reliable and safe tools for stable gene transfer in a wide variety of mammalian cells. Unlike other vectors derived from oncoretroviruses, they allow for stable gene delivery into most nondividing primary cells. This is why LVs are becoming useful and promising tools for future gene and cell therapy approaches. Lentivectors (LVs) derived from HIV-1 have gradually evolved to display many desirable features aimed at increasing both their safety and their versatility. These latest designs are reviewed in this unit. This unit also describes protocols for production and titration of LVs that can be implemented in a research laboratory setting, with an emphasis on standardization to improve transposability of results between laboratories.
科研通智能强力驱动
Strongly Powered by AbleSci AI