Gene Editing Cell Line Generation

CRISPR as a highly efficient gene editing tool can manipulate the genome of a cell to achieve gene knockout, knock-in, targeted gene mutation in specific cells. Gene-edited cell lines generated by CRISPR/Cas9 technology can be widely used for gene function research, signaling, recombinant protein preparation, drug discovery, and disease mechanism of action research. Creative Biogene's scientists utilize advanced CRISPR technology to efficiently and precisely modify specific genes in a variety of cell types, including but not limited to mammalian cells, stem cells, and other cells, based on the research needs of our clients. We are committed to providing comprehensive and efficient gene editing cell line generation services to accelerate your research.


Sign In or Register to comment.