Our platform specializes in the discovery and development of AAV vectors for targeted gene therapy in ophthalmology.
Adeno-associated viruses (AAVs) are small, non-pathogenic viruses that have become indispensable tools in preclinical ophthalmology research. Our platform offers comprehensive AAV development services, from design and engineering to production and characterization. We specialize in developing vectors optimized for ocular gene delivery, addressing challenges such as retinal penetration and transduction efficiency.
AAV in Preclinical Ophthalmology StudiesOur platform integrates cutting-edge artificial intelligence (AI) to revolutionize the AAV vector discovery process. By leveraging AI algorithms, we achieve faster discovery cycles, multi-dimensional optimization, and enhanced vector performance.
Our AAV vector development services encompass the entire workflow, from design and engineering to production and characterization. We provide customized solutions for diverse ocular gene therapy applications.
Learn MoreOur recombinant AAV (rAAV) vector development services leverage the latest advancements in vector engineering to provide highly efficient and targeted gene delivery solutions for ocular diseases.
Learn MoreWe offer customized solutions tailored to your specific needs, from individual service components to comprehensive program management. Contact us today to discuss your project.