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Updated: Nov 6, 2025

Efficient Generation of hiPSC Neural Lineage Specific Knockin Reporters Using the CRISPR/Cas9 and Cas9 Double Nickase System
Published on: May 28, 2015
Generation of mouse hippocampal neural precursor cell lines with CRISPR/Cas9-mediated gene knockouts
Sara Zocher1, Gerd Kempermann1
1German Center for Neurodegenerative Diseases, Tatzberg 41, Germany and Center for Regenerative Therapies Dresden, Fetscherstraße 101, 01307 Dresden, Germany.
Abstract:
Genetic manipulation of neural precursor cells is an important tool to study mechanisms underlying proliferation, fate specification, and neuron formation. The CRISPR/Cas9 system enables efficient genome editing but requires the clonal expansion of cells containing the desired mutation. Here, we describe a protocol for the effective generation of clonal mouse hippocampal neural precursor lines with CRISPR/Cas9-based gene knockouts. Edited cell lines can be used to investigate gene regulatory networks driving neuronal differentiation and for modeling of diseases that involve hippocampal neurogenesis. For complete details on the use and execution of this protocol, please refer to Pötzsch et al. (2021).
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