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Updated: Aug 12, 2026

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Packaging HIV- or FIV-based Lentivector Expression Constructs & Transduction of VSV-G Pseudotyped Viral Particles
Published on: April 8, 2012
Lentiviruses as gene transfer agents for delivery to non-dividing cells
1Cell Genesys, Foster City, CA, USA. luigin@cellgenesys.com
Current Opinion in Biotechnology
|November 20, 1998
Abstract:
Lentiviral vectors are proving to be effective agents for the direct delivery and sustained expression of a transgene in several tissues, including brain, retina, muscle and liver. Significant progress was achieved in the biosafety of HIV-derived vectors by eliminating all the viral sequences non-essential for transduction. Other vectors have also been developed from non-primate lentiviruses.

