Novel Approaches to Overcome CRISPR In Vitro Delivery Challenges
In order for CRISPR gene editing to reach its full potential, we must develop in vitro delivery approaches that will allow us to work with hard-to-transfect cells, large repair templates, multiplex editing projects, and minimise off-target effects.
By Dr. Paul Monnier, Field Application Scientist
This article is taken from European Biopharmaceutical Review October 2020, pages 34-37. © Samedan Ltd.
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European Biopharmaceutical Review | October 2020
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