Gene Editing

Support for CRISPR/Cas9 based gene editing approaches targeting viral and cellular genes delivered by transient or stable transfection, viral vector transduction, for in vitro and in vivo approaches. Guidance is provided on target selection, bioinformatics screening, validation of target modification, and assessment of safety ands efficacy.

For additional information, please contact Rafal Kaminski, PhD at [click-for-email].