Viral transduction is a method of gene transfer that uses viruses to deliver genetic material into cells. It is commonly used in research and gene therapy to introduce new genes or modify existing ones in target cells. The virus is engineered to be replication-defective, meaning it can infect cells but cannot produce new viral particles, thus preventing uncontrolled viral spread. Commonly used viral vectors include lentiviruses, adenoviruses, and adeno-associated viruses (AAVs).
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