The combined activity of the adenovirus-derived genes on the helper plasmid with the rAAV genes on the second plasmid proved sufficient to generate functional rAAV particles containing the ...

The process of creating adenoviral vectors involves inserting the transgene into a small shuttle plasmid so that the transgene cassette can be excised with two restriction enzymes with almost unique ...

A 1984 paper by Paul Hermonat and Nicholas Muzyczka offered the first demonstration that AAV might provide a safe and effective vehicle for transgene delivery, with helper adenovirus infection ...

first-generation adenovirus (FGAd), helper-dependent adenovirus (HDAd), Lentivirus (LV), Retrovirus (RV), and G-deleted Rabies (RaV). In addition, we have a variety of supporting services available ...