www.genecopoeia.com
Delivery of exogenous DNA to cultured cells and animals is a fundamental strategy for modern molecular biology, functional genomics, and gene therapy. While plasmid transfection is widely used for routine DNA delivery into cultured cells, the use of viral vectors is often advantageous, especially for cells that are refractory to transfection. Further, viral vectors remain the only practical option for DNA delivery to tissues in vivo. In this webinar, we will compare lentiviral systems with adeno-associated virus (AAV) systems, how to decide which system is appropriate for a specific scenario, and how GeneCopoeia’s powerful suite of lentiviral and AAV products and services can help you with your DNA delivery applications.

For more information, please visit: www.genecopoeia.com

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