Adeno-associated Virus Services
Adeno-associated virus (AAV) vectors are currently among the most frequently used viral vectors for gene therapy. AAV is an ideal virus to use as the vehicle for gene transfer because:
- AAV is a simple, easily manipulated virus
- AAV can deliver genes to both dividing and non-dividing cells
- AAV can deliver genes to a wide variety of tissue types from muscle to brain
- AAV has never been shown to cause disease
- AAV elicits only weak immunologic responses
- AAV allows expression of proteins in the host cells for long periods of time
Welgen currently offers AAV pre-made control and services (conventional or double-stranded, also called self complementary) for AAV2, AAV5, AAV8, AAV9 and AAV-DJ serotypes.
Contact/Request a Quote| Item ID | Service |
| SA1100 | Standard AAV Production |
| SA 2000 | Customer AAV Construction and Production |