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Addressing plasmid DNA challenges in large-scale manufacturing of recombinant adeno-associated virus and lentivirus using enzymatically generated dbDNA

Whitepaper

Recent advances in gene therapy have increased the use of recombinant adeno-associated viruses (rAAV) and recombinant lentiviruses (rLV) as gene delivery vectors. However, challenges remain in scaling up their production due to reliance on plasmid DNA (pDNA).

Namely, traditional pDNA manufacturing methods face bottlenecks, including scalability issues and regulatory concerns related to bacterial contaminants and antibiotic resistance genes.

This whitepaper explores the use of doggybone DNA (dbDNATM), a synthetic alternative to pDNA, for producing rAAV and rLV. The results indicate that dbDNA offers a promising solution for overcoming limitations associated with pDNA in large-scale viral vector manufacturing. 

Using dbDNA for Recombinant AAV and LV Production - Thermo Fisher Scientific