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A pair of primers facing at the double-strand break site enables to detect NHEJ-mediated indel mutations at a 1-bp resolution

The introduction of small insertion/deletion (indel) mutations in the coding region of genes by the site-specific nucleases such as Cas9 allows researchers to obtain frameshift null mutants. Technically simple and costly reasonable genotyping methods are awaited to efficiently screen the frameshift...

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Detalles Bibliográficos
Autores principales: Ijaz, Faryal, Nakazato, Ryota, Setou, Mitsutoshi, Ikegami, Koji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270360/
https://www.ncbi.nlm.nih.gov/pubmed/35804017
http://dx.doi.org/10.1038/s41598-022-15776-5