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Chapters
- 00:04Title
- 01:23Design and Cloning of gRNAs into the CRISPR Vector
- 05:51Intraperitoneal Injection of rAAVrh.74-CRISP into Neonatal mdx Mice
- 06:38Analysis of Dystrophin Expression by Immunofluorescence Staining
- 07:31Results: rAAV-Mediated Gene Editing Restores Dystrophin Expression in Dystrophic Mice
- 08:34Conclusion
Here we provide a detailed protocol to carry out in vivo cardiac gene editing in mice using recombinant Adeno-Associated Virus(rAAV)-mediated delivery of CRISPR. This protocol offers a promising therapeutic strategy to treat dystrophic cardiomyopathy in Duchenne muscular dystrophy and can be used to generate cardiac-specific knockout in postnatal mice.
