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Lentivirus Vector Research and Development

Lentiviral vectors have been instrumental in the development of chimeric antigen receptor (CAR) T cell therapy, by delivering the CAR construct into T cells. Here they offer stable integration of genetic material into host cells without relying on cell division for transduction. Despite these advantages, systemic delivery of lentiviral vectors remains a challenge and additional improvements are required for safer and more efficient application.

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Viral Vector Development – from cloning to transduction

 

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*All products are for Research Use Only (RUO).

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