Larcombe et al., 2019 - Google Patents
Production of high-titer lentiviral particles for stable genetic modification of mammalian cellsLarcombe et al., 2019
- Document ID
- 12438290735194376206
- Author
- Larcombe M
- Manent J
- Chen J
- Mishra K
- Liu X
- Nefzger C
- Publication year
- Publication venue
- Mouse Cell Culture: Methods and Protocols
External Links
Snippet
Lentiviral gene transfer technologies exploit the natural efficiency of viral transduction to integrate exogenous genes into mammalian cells. This provides a simple research tool for inducing transgene expression or endogenous gene knockdown in both dividing and …
- 210000004962 mammalian cells 0 title abstract description 4
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- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
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- C12N2740/00—Reverse Transcribing RNA Viruses
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- C12N2740/13041—Use of virus, viral particle or viral elements as a vector
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- C12N5/06—Animal cells or tissues; Human cells or tissues ; Not used, see subgroups
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