Gene editing is a critical capability, particularly in the fast-growing field of cell and gene therapy. However, scientists must take care that their gene edits do not result in unintended consequences. Technologies like CRISPR-Cas9 can generate multiplex edits, but the required multiple double strand breaks in the host cell genome may lead to cell toxicity, off-target editing, and unwanted genomic rearrangements.
Watch this on-demand webinar to learn how base editing with the novel Pin-point™ platform can achieve efficient and precise complex multiplex edits of cell lines, while decreasing the potential of unintended consequences.
In this webinar, you will learn:
The Pin-point platform technology is available for clinical study and commercialization under a commercial license from Revvity. Pin-point reagents are available for research use only.