Adeno-associated virus (AAV) vectors represent a class of small, non-enveloped, replication-defective DNA viruses that are being developed for human gene therapy. AAV is the only non-pathogenic ...

It is a true producer cell line that has Rep, Helper, Cap, and gene of interest (GOI) stably integrated into the host cell’s genome, and it requires only a single induction step to initiate AAV ...

Adeno-associated virus (AAV)-based systems have also been ... for routine transfections in research labs. Another physical transfection approach is Magnetofection, a new method that associates ...

Adeno-associated virus (AAV) is rapidly becoming the go-to biological delivery method for the latest gene therapy breakthroughs. AAV has an efficacy and safety profile that makes it an ideal ...

Adeno-associated virus (AAV) vectors are the leading platform for gene delivery in the treatment ... These ratios can vary dramatically in vector preparations produced by standard transient ...