Human pluripotent stem cells (hPSCs) hold great promise for the study and treatment of human disease owing to their ability to differentiate into many specialized cell types of the human body. The use of genome editing tools to generate specific DNA variants in hPSCs, by either introducing disease-specific mutations or correcting genetic aberrations, provide more accurate modeling of human disease when differentiated into human-derived tissues. Advances in genetic tools such as zinc-finger nucleases (ZFNs), transcription activator-like effector nucleases (TALENs) or most recently clustered regularly interspaced short palindromic repeat (CRISPR), have improved the ease and efficiency of genome editing in hPSCs.
Explore the resources below to support your genome editing using hPSCs.
View this webinar presentation by Dr. Ashley Watson to learn more about optimized workflows for CRISPR-Cas9 genome editing in difficult-to-manipulate cell types, including human pluripotent stem cells and primary T cells.View Now >