Lentivector

Lentivectors for Stable Gene Delivery and Long-Term Expression

Explore Gentaur’s specialized portfolio of Lentivectors, engineered for efficient, stable gene delivery into dividing and non-dividing cells. Lentiviral vectors are indispensable tools in gene therapy, CRISPR/Cas9 gene editing, RNA interference (RNAi), and cell line engineering, offering long-term transgene expression and high transduction efficiency across a wide range of mammalian cell types.

Our collection includes pre-made lentiviral plasmids, customizable lentiviral vector backbones, and ready-to-use pseudotyped viral particles, optimized for high titer and minimal cytotoxicity. All vectors are manufactured under rigorous quality control standards and include detailed maps and full sequence data.