Skip to main content
. 2021 Jul 13;11(3):217–233. doi: 10.1007/s13534-021-00199-4

Fig. 5.

Fig. 5

CRISPR-Cas9 system delivery using viral vectors. Adeno-associated virus (AAV), adenovirus (AVs), and lentivirus (LV) deliver the Cas9 protein in a plasmid DNA format; these viruses can infect a wide array of cells and exhibit a high gene editing capacity