Cargando…
Engineering of Primary Human B cells with CRISPR/Cas9 Targeted Nuclease
B cells offer unique opportunities for gene therapy because of their ability to secrete large amounts of protein in the form of antibody and persist for the life of the organism as plasma cells. Here, we report optimized CRISPR/Cas9 based genome engineering of primary human B cells. Our procedure in...
Autores principales: | Johnson, Matthew J., Laoharawee, Kanut, Lahr, Walker S., Webber, Beau R., Moriarity, Branden S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092381/ https://www.ncbi.nlm.nih.gov/pubmed/30108345 http://dx.doi.org/10.1038/s41598-018-30358-0 |
Ejemplares similares
-
A Pan-RNase Inhibitor Enabling CRISPR-mRNA Platforms for Engineering of Primary Human Monocytes
por: Laoharawee, Kanut, et al.
Publicado: (2022) -
Highly multiplexed genome engineering using CRISPR/Cas9 gRNA arrays
por: Kurata, Morito, et al.
Publicado: (2018) -
CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells
por: Kluesner, Mitchell G., et al.
Publicado: (2021) -
Engineered CRISPR-Cas9 nucleases with altered PAM specificities
por: Kleinstiver, Benjamin P., et al.
Publicado: (2015) -
Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors
por: Webber, Beau R., et al.
Publicado: (2019)