Adeno-associated virus (AAV) is a powerful vector system used to transduce cells in vivo. Recombinant AAV can efficiently deliver genetic material to both dividing and non-dividing cells. AAV is replication-defective, nonpathogenic, and noncytotoxic, and can maintain physiologically relevant expression levels in cells and tissues. Currently, AAV has become one of the most promising viral vectors for gene therapy.
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