
Adeno-associated virus (AAV) particles are packaged and purified viruses designed to insert transgenic material into mammalian cells. These AAV viruses are carefully produced with defined titer amounts for research applications involving gene expression, gene editing, cell line development, and gene therapy. AAV vectors generally have an insert size of up to 5 kb that can produce transient or stable gene expression. AAV also features tissue specificity based on its different capsid serotypes. Visit the supplier page for more information.
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