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High Complexity AAV3 Capsid Library for Targeted Human Gene Therapy
Allows Efficient Development of Specialized Vectors for Targeted Gene DeliveryThis adeno-associated virus (AAV) vector library combines tens of millions of actual capsid variants in an AAV3 backbone in order to allow the isolation of specialized variants with increased transduction efficiency and high specificity for particular organs or cell populations,...
Published: 6/27/2021
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Inventor(s): Sergei Zolotukhin, Damien Marsic
Keywords(s): AAV Vectors, Gene Therapy, Liver
Category(s): Technology Classifications > Human Health Care, Technology Classifications > Human Health Care > Gene Therapy
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