Gene Therapy & Cell Engineering
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Gene Therapy & Cell Engineering
High-quality viral vectors (AAV,Lentivirus, Adenovirus) and plasmid DNA production for gene therapy and vaccine research. We also develop stable cell lines for drug screening and functional studies.
Viral Vector Production
High-quality AAV, Lentivirus, and Adenovirus production for gene therapy research.
Plasmid Production
Small- and large-scale plasmid DNA production for gene therapy and vaccine development.
Establishing Viral Vectors and Plasmids for Clinical Supply
- Lentivirus: Research-Grade and Clinical Grade Vector Products.
- Retrovirus: Research-Grade and Clinical Grade Vector Products.
- Adenovirus: Research-Grade and Clinical Grade Vector Products.
The Power of our Viral Vectors
- Efficient Transduction: Effectively transduce both dividing and non-dividing cells for long-term stable expression.
- Versatile Applications: Leverage the versatility of Lentiviral vectors across a wide range of research disciplines.
- Robust Performance: Rely on the unparalleled efficiency and reliability of our cutting-edge Lentiviral technology.
Stable Cell Line Development
Generation of cell lines with reporter genes (GFP, Luciferase, etc.) for drug screening and functional studies.