This poster presents a human-based screening platform developed by Ncardia to evaluate the transduction efficiency, cytotoxicity, and overall performance of multiple AAV serotypes in hiPSC-derived cardiomyocytes, supporting more informed vector selection for gene therapy applications.
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Quantitative data showing that AAV1 and AAV5 achieve the highest transduction efficiencies, while AAV4 shows no measurable transduction in this system