AAV Custom Production
With a curated gene library in our freezers, productions are typically delivered within 2-4 weeks from design.
Why Use Our Custom
AAV Production Service?
Tailored Gene Delivery
Create AAV vectors with specific genes, promoters, or serotypes for unique research needs.
Reliable Quality Control
Ensure consistent, high-quality vectors with accurate titers and purity.
Versatility Across Applications
Support gene therapy, disease modeling, functional studies, and more.
Scalability for Trials
Produce vectors at scale for preclinical trials with consistency
The AAV Production Process
PROCESS
4-5 weeks to complete
Cloning
Transfection
Packaging
Purification
Analytics
Custom plasmids
in 2 weeks
Viral packaging, purification, and analytics in 2-4 weeks
Custom plasmids in 2 weeks
VIRAL PACKAGING, PURIFICATION, AND ANALYTICS IN 2-4 WEEKS
Cloning
Transfection
Packaging
Purification
Analytics
How to Get Started
For a complete service from pAAV cloning, provide
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Over-expression AAV construct, 5-10 ug plasmid DNA, vector map, and sequence for your plasmidX
For shRNA AAV service, the exact RNAi sequence to be cloned into the recombinant AAV vector or your shRNA plasmidX
For gRNA AAV, the gRNA sequence.
For plasmid packaging, provide
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FX 150-600ug of your pAAV plasmidX
The plasmid map/sequence for viral production
If you don’t have any starting material,
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We can create AAV to overexpress or silence any genes from any species. Our scientists will discuss your needs and recommend suitable AAV constructs before producing them based on the agreed specifications.
Request A QuoteFrom Bench to Breakthrough: Inside Our AAV Production & Success Stories
Why Use Vector Biolabs
High Customization
Tailor-made AAV vectors designed to meet specific research needs, including unique promoters, serotypes, and gene constructs.
Reliable Quality
Consistent production standards ensure high-quality viral vectors with accurate titers and purity, critical for reproducible results.
Broad Application Scope
Supports a variety of applications, including gene therapy, disease modelling, and functional studies.
Efficient Turnaround
AAV can transduce a wide range of cell types, including dividing and non-dividing cells.
Gene Expression
Streamlined processes enable timely delivery of custom AAV vectors, helping researchers meet project deadlines without compromising quality.