Multiple Serotypes
A range of AAV serotypes
for delivery to different tissues and organs.
AAV (adeno-associated virus) is a safe, efficient gene delivery vector for research applications including target gene overexpression, knockdown, in vivo knockout and Cre-dependent expression,
meeting diverse basic and translational research needs.
A range of AAV serotypes
for delivery to different tissues and organs.
Optimized production processes,
Viral titers up to 1×1013 vg/mL。
Efficient transduction with strong tissue specificity,
for in vivo studies in diverse animal models.
High-quality AAV packaging tailored to your research goals and experimental requirements.
Efficient AAV-mediated target gene expression.
shRNA, miRNA and other
gene silencing approaches.
Using CRISPR/Cas systems
for in vivo gene editing.
Conditional systems such as DIO / FLEX
expression systems.
1×1013 vg/mL
For experiments in diverse animal models
>4.7 kb
Beyond the capacity of a single vector,
for large gene delivery
Multiple quality checks for high-quality vectors
Tailored to your experimental needs, with
custom solutions and technical support throughout.
A standardized service workflow to advance your research efficiently.
Define research goals and requirements
Recommend a suitable serotype and plan
Gene synthesis and vector construction
Small- or large-scale production
Titer, purity, endotoxin and more
Dry ice shipping and expert support
Please complete the information below. We will contact you promptly to discuss a suitable experimental plan.