May 7, 2021
Date: May 7, 2021
Duration: 20 Min
Sponsored by Mirus Bio
This webcast features: Leisha Kopp, Applications Scientist, Mirus Bio
Recombinant adenoassociated virus (AAV) and lentivirus (LV) are critical components of gene and cell therapies, which show incredible promise for the treatment of disease. Accordingly, the need for large-scale manufacture of safe and effective viral vectors has never been greater. Here, we present:
Optimization strategies for AAV and LV generation in both adherent and suspension HEK 293 cells
LV and AAV enhancers that further increase functional virus titers over previously optimized conditions
How TransIT-VirusGEN® Transfection Reagent and Kits can expand manufacturing capabilities for gene and cell therapies
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