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Cas9 overexpressing cell line development provides a robust platform for CRISPR-based genome editing. By engineering cell lines to stably express high levels of the Cas9 nuclease, researchers can achieve efficient gene knockouts, knock-ins, and functional screenings. This approach enhances the reliability and precision of gene editing experiments and accelerates research into gene function, disease modeling, and therapeutic development.
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Category
Research -
Created
Monday, 12 May 2025 -
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cailynn johnson
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