Our focus
We develop technologies for targeted and regulated expression of therapeutic genes
Lentiviral vector particlesLentiviral vectors (LVs) are the most efficient gene-delivery tools. The engineered viral particles can transduce most mammalian cells, including stem cells and neuron. We design gene-delivery systems based on the lentiviral backbone and provide them as plasmids or ready to use Lentiviral particles that can express the gene of interest in a constitutive, inducible or tissue-specific manner.
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Cell lines expressing the Gene-of-InterestLentiStem biotech specializes in hard-to-modify cells, such as primary tumor cells, T-cells, B-cell lines, human Mesenchymal Stem cells or induced Pluripotent Stem cells. Lentistem can provide you high quality, stable-cell lines expressing your gene-of-interest in constitutive, inducible or tissue-specific manner.
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