The CRISPR/Cas9 system can efficiently edit the gene of your interest
The Xfect RNA Transfection Reagent used for CRISPR/Cas9 gene editing
The Cas9/sgRNA can be delivered into the target cells by AAV and lentiviral systems
The Cas9/sgRNA can be delivered into cells by all in one plasmid
The gesicles are the unique technology also used for transport Crispr/Cas9 complex into the cells
The Electroporation ready Cas9 system for gene editing mediated by CRISPR/Cas9