CRISPR donor vector construction

by cailynn on May 28th, 2025 04:15 AM

CRISPR donor vector construction enables precise genetic modifications through homology-directed repair (HDR) or non-homologous end joining (NHEJ). These vectors facilitate gene insertions, corrections, and functional tagging, supporting therapeutic development and functional genomics. Optimized vector design ensures high accuracy, efficient genome editing, and stable delivery formats for research and clinical applications.