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Streamlining mouse genome editing by integrating AAV repair template delivery and CRISPR-Cas electroporation

Streamlining mouse genome editing by integrating AAV repair template delivery and CRISPR-Cas electroporation

Natalia Moncaut ¹

Natalia Moncaut ¹

¹Genome Editing and Mouse Models, Cancer Research UK Manchester Institute, The University of Manchester, Manchester, UK. natalia.moncaut@cruk.manchester.ac.uk.

⁰Genome Editing and Mouse Models, Cancer Research UK Manchester Institute, The University of Manchester, Manchester, UK. natalia.moncaut@cruk.manchester.ac.uk.

Lab Animal +

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April 10, 2024

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April 10, 2024

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Summary

No abstract available on PubMed

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Related Concept Videos

CRISPR

CRISPR

Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...

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