Cargando…
Generating Single Cell–Derived Knockout Clones in Mammalian Cells with CRISPR/Cas9
CRISPR/Cas9 technology enables the rapid generation of loss‐of‐function mutations in a targeted gene in mammalian cells. A single cell harboring those mutations can be used to establish a new cell line, thereby creating a CRISPR‐induced knockout clone. These clonal cell lines serve as crucial tools...
Autores principales: | Giuliano, Christopher J., Lin, Ann, Girish, Vishruth, Sheltzer, Jason M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741428/ https://www.ncbi.nlm.nih.gov/pubmed/31503414 http://dx.doi.org/10.1002/cpmb.100 |
Ejemplares similares
-
Generation of gene-of-interest knockouts in murine organoids using CRISPR-Cas9
por: Huber, Anne, et al.
Publicado: (2023) -
Generation of mouse hippocampal neural precursor cell lines with CRISPR/Cas9-mediated gene knockouts
por: Zocher, Sara, et al.
Publicado: (2021) -
CRISPR-Cas9-induced gene knockout in zebrafish
por: Medishetti, Raghavender, et al.
Publicado: (2022) -
Protocol for generating monoclonal CRISPR-Cas9-mediated knockout cell lines using RNPs and lipofection in HNSCC cells
por: Geyer, Fabian, et al.
Publicado: (2023) -
Generation of gene-of-interest double allele knockout clones in primary human T cells by CRISPR
por: Wu, Ling, et al.
Publicado: (2023)