AAV Production Service
Safely & efficiently deliver target genes into your cells
Adeno-associated virus (AAV) is a non-enveloped virus that can be engineered to efficiently deliver DNA sequences of interest into target cells with a low immunogenicity. Because of these unique characteristics, AAV-mediated genome editing has emerged as a highly promising gene delivery method. AMSBIO provides a service to make ready-to-use AAV packaging service for any specific gene, shRNA or miRNA. We will sub-clone your selected genes into our AAV expression vectors and produce expression AAV for each gene.
Our Services
Over-expression AAV construction
You can choose the promoter and a tag.
Either you provide target templates or we synthesize or obtain it from a cDNA collection. We construct the AAV clone and generate ready-to-use expression AAV. High titer AAV service is available.
Ensure that you choose the right AAV serotype for your application.
Why use AMSBIO's AAV services?
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- Transfect both dividing and non-dividing cells
- Ready-to-use
- No host-genome integration & stable expression
- Easy to produce at high viral titre (helper free)
- Does not elicit significant immune response in vivo
- Can be used for in vivo gene delivery
- Multiple serotypes available
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Serotype Selection
| Tissue Type | Recommended AAV Serotypes |
|---|---|
| Muscle | AAV1, AAV6, AAV8, AAV9 |
| Liver | AAV8, AAV9, AAV-DJ |
| Lung | AAV5, AAV6, AAV9 |
| Central Nervous System | AAV1, AAV5, AAV8, AAV9, AAV-DJ |
| Retina | AAV1, AAV2, AAV5, AAV8 |
| Pancreas | AAV8 |
| Kidney | AAV2, AAV9 |
| Heart | AAV1, AAV8, AAV9 |
Lentivirus & Adenovirus & AAV Request Form
Let's get started
Complete our service request form and we will contact you to discuss your requirements.