Features:
– Excellent gene delivery efficiency in most cell types including dividing and non-dividing or primary cells.
– Multiple serotypes (AAV1, AAV2, AAV5, AAV6, AAV8, AAV9).
– Integration into chromosome 19 of host genome.
– Induce efficient gene silencing.
Wide Choice of AAV cis Vectors:
Service Description:
1. Synthesize and clone shRNA into AAV cis vectors.
2. Pilot scale transfection of AAV·HT™ 293 cell into 10×150 mm plates.
3. Harvest rAAV followed by column filtration.
4. Desalting, filter sterilization, and AAV titration via qPCR.
Required Materials: Target gene sequence or validated shRNA sequence.
Turnaround Time: 3~4 weeks.
Deliverables: >0.8 ml rAAV vector at >1E+12 VG/ml* will be delivered for in vitro application ONLY.
We offer discount for new customer, please request a quote with us today.
We also offer truncated custom shRNA AAV service, please request a quote with us today.
* Final viral yield may depend on the nature of transgene.
