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Comprehensive Viral Vector & Stable Cell Development Solutions
End-to-end viral vector production supporting construct development, plasmid preparation, viral packaging, purification, and quality control. Flexible service options enable efficient generation of high-quality vectors for in vitro, in vivo, and preclinical research applications
Custom adeno-associated virus (AAV) vectors designed for precise gene delivery and expression. Supports applications including transgene expression, RNAi-mediated knockdown, CRISPR genome editing, and tissue-specific gene modulation in preclinical and in vivo studies.
Packaging of customer-supplied AAV transfer plasmids into purified viral particles. Production includes packaging, purification, and QC to deliver high-quality AAV suitable for in vivo experiments and functional studies.
Lentiviral vector development and production enabling stable gene delivery in dividing and non-dividing cells. Supports transgene overexpression, shRNA or miRNA knockdown, CRISPR genome editing, and HDR-based genome modification.
Conversion of validated lentiviral transfer plasmids into high-titer viral particles for experimental use. Packaging and purification workflows produce lentivirus suitable for reliable transduction and stable gene expression studies.
Recombinant adenoviral vectors for high-efficiency transient gene expression without genomic integration. Commonly used for functional genomics, pathway studies, and genome editing applications.
High-yield adenovirus amplification using the Ad.MAX™ helper-virus–free system. Designed for efficient viral rescue and scalable production for research applications.
High-quality, customized stable cell lines tailored to your specific research or production needs, leveraging proven viral vector systems and comprehensive, rigorous quality control to ensure consistency, reliability, and reproducibility across applications.
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