摘要:
Sequences of adeno-associated virus capsids and vectors and host cells containing these sequences are provided. Also described are methods of using such host cells and vectors in production of rAAV particles. AAV-mediated delivery of therapeutic and immunogenic genes using the vectors of the invention is also provided.
摘要:
Sequences of adeno-associated virus capsids and vectors and host cells containing these sequences are provided. Also described are methods of using such host cells and vectors in production of rAAV particles. AAV-mediated delivery of therapeutic and immunogenic genes using the vectors of the invention is also provided.
摘要:
A method for isolating AAV viruses from cellular DNA of mammalian tissues comprises transfecting the digested DNA into cells, rescuing the virus and amplifying it through serial passages in the presence of adenovirus helper functions. Kits useful for performing this method are also provided.