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AAV Vector Research and Development

AAVs play a crucial role in CAR-T cell therapy, with constructs designed to encode and deliver the chimeric antigen receptor (CAR) into host cells. Due to its low immunogenic profile and a diverse tropism for human tissues, it has demonstrated tremendous potential in the development of human gene therapies, with room for further improvement.

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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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