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AAV (Adeno-Associated Virus) vector production refers to the process of creating engineered viral particles that deliver genetic material into target cells. AAV vectors are commonly used in gene therapy due to their safety profile, low immunogenicity, and ability to efficiently transduce various cell types. The production process involves plasmid design, transfection of host cells (typically HEK293 cells), and purification to achieve high-quality, high-titer AAV vectors suitable for research or clinical applications.
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