Construction and production of AAV vectors

The AAV vectors are derived from adeno-associated viruses. They make it possible to transfer a small size of DNA (4kb) and without integration into the DNA of the target cell. This avoids uncontrolled insertion which could disrupt cell function.
The PFV accepts your ready-to-use AAV-transgene vectors but can also take charge of the custom construction of your AAV-gene vectors of interest and proceed with the production of AAV viral particles of different serotypes.