AAV transduction
Adeno-associated virus (AAV) is a popular choice for delivering genes to cells in vivo. Several features of the virus, including minimal pathogenicity, sustained viral persistence, and broad cell-type infectivity, make AAV-mediated gene delivery an effective strategy for creating disease models and studying gene function in animal models.
Adeno-associated virus (AAV) is a popular choice for delivering genes to cells in vivo. Several features of the virus, including minimal pathogenicity, sustained viral persistence, and broad cell-type infectivity, make AAV-mediated gene delivery an effective strategy for creating disease models and studying gene function in animal models.
The AAVpro series is a suite of products for generating high titers of transduction-ready recombinant AAV particles—from expression, packaging, and extraction, to purification and titration.
Featured product: try our unique AAVpro Purification Kit Maxi (All Serotypes)
AAV purification kits
Obtain high yields and high purity of AAV with these easy-to-use purification technologies.
AAV product pages
AAV production workflow
Adeno-associated virus (AAV) is a non-enveloped, single-stranded DNA virus that can infect both nondividing and dividing cells. AAV is thought to be nonpathogenic to humans and only replicates in the presence of a helper virus. These features have made AAV a useful tool for gene delivery to a wide variety of cell types and an attractive vector for gene therapy.
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