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A simple and highly efficient method for multi‐allelic CRISPR‐Cas9 editing in primary cell cultures

BACKGROUND: CRISPR‐Cas9‐based technologies have revolutionized experimental manipulation of mammalian genomes. None‐the‐less, limitations of the delivery and efficacy of these technologies restrict their application in primary cells. AIMS: To create an optimized protocol for penetrant, reproducible,...

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Detalles Bibliográficos
Autores principales: Hoellerbauer, Pia, Kufeld, Megan, Arora, Sonali, Wu, Hua‐Jun, Feldman, Heather M., Paddison, Patrick J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685144/
https://www.ncbi.nlm.nih.gov/pubmed/32721120
http://dx.doi.org/10.1002/cnr2.1269