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The TOP vector: a new high-titer lentiviral construct for delivery of sgRNAs and transgenes to primary T cells

Efficient delivery of nucleic acids for the engineering of primary T cells is central to the study of the basic biology of these key immune effector cells and has clinical implications. To date, lentiviral vectors delivering guide RNAs for CRISPR-Cas9 editing are not optimal for use in primary cells...

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Detalles Bibliográficos
Autores principales: Humes, Daryl, Rainwater, Stephanie, Overbaugh, Julie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732963/
https://www.ncbi.nlm.nih.gov/pubmed/33335945
http://dx.doi.org/10.1016/j.omtm.2020.10.020

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