Gene Editing

Since the TALEN and CRISPR technologies were invented, gene-editing in human cells became feasible both in vitro and in vivo. Human genetic disease models can be quickly established in the cell lines or laboratory animals for mechanism study and drug discovery. We have extensive experience in generating knockout, knock-in, insertion, or deletion in human cells. We established standard protocols for our gene editing service with a predictable timeline. Our service can facilitate and power your research.