Adeno associated virus (AAV) is an important viral vector for gene therapy. It is useful because of its broad tropism, minimal immunogenicity, lack of association with any disease, and the ability to achieve efficient and persistent gene transfer. AAV has limited packaging capability with about 5 kb of single stranded DNA. The vector genome is completely user-defined to deliver transgenic content to a target cell, although the transgene cargo must be flanked by inverted terminal repeats (ITRs), which is the only element retained from the native virus in the vector genome. AAV Genome Titer https://qvirus.creative-biogene.com/services/aav-genome-titer-assay.html
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AAV Genome Titer

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Adeno associated virus (AAV) is an important viral vector for gene therapy. It is useful because of its broad tropism, minimal immunogenicity, lack of association with any disease, and the ability to achieve efficient and persistent gene transfer. AAV has limited packaging capability with about 5 kb of single stranded DNA. The vector genome is completely user-defined to deliver transgenic content to a target cell, although the transgene cargo must be flanked by inverted terminal repeats (ITRs), which is the only element retained from the native virus in the vector genome. AAV Genome Titer https://qvirus.creative-biogene.com/services/aav-genome-titer-assay.html

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