CRISPR
CRISPR/Cas9 Genome Editing
In-vitro Mutagenesis
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Updated: Mar 6, 2026

Efficient Genome Editing of Mice by CRISPR Electroporation of Zygotes
Published on: December 16, 2022
Benedikt Wefers1, Sanum Bashir2, Jana Rossius3
1German Center for Neurodegenerative Diseases (DZNE), Feodor-Lynen Str. 17, 81377 Munich, Germany; Helmholtz Zentrum München, German Research Center for Environmental Health, Institute of Developmental Genetics, Ingolstädter Landstr. 1, 85764 Neuherberg, Germany.
CRISPR/Cas9 gene editing enables rapid creation of targeted mouse mutants for research. This guide details designing alleles, preparing reagents, editing zygotes, and genotyping offspring for biomedical applications.
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