Amplification-free RNA detection with CRISPR–Cas13
The authors develop a platform (SATORI) that enables accurate and rapid detection of single-stranded RNA at a single-molecule level without a pre-amplification step. As a proof-of-concept, they demonstrate its utility in detecting the SARS-CoV-2 N gene at a minimum concentration of ~5 fM, which is m...
Guardado en:
Autores principales: | Hajime Shinoda, Yuya Taguchi, Ryoya Nakagawa, Asami Makino, Sae Okazaki, Masahiro Nakano, Yukiko Muramoto, Chiharu Takahashi, Ikuko Takahashi, Jun Ando, Takeshi Noda, Osamu Nureki, Hiroshi Nishimasu, Rikiya Watanabe |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/74b9926452694c26addf7fb0b414e93e |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Real-space and real-time dynamics of CRISPR-Cas9 visualized by high-speed atomic force microscopy
por: Mikihiro Shibata, et al.
Publicado: (2017) -
Precise CAG repeat contraction in a Huntington’s Disease mouse model is enabled by gene editing with SpCas9-NG
por: Seiya Oura, et al.
Publicado: (2021) -
Ultrastructure of influenza virus ribonucleoprotein complexes during viral RNA synthesis
por: Masahiro Nakano, et al.
Publicado: (2021) -
Structural and functional insights into IZUMO1 recognition by JUNO in mammalian fertilization
por: Kazuki Kato, et al.
Publicado: (2016) -
Crystal structure of the plant receptor-like kinase TDR in complex with the TDIF peptide
por: Junko Morita, et al.
Publicado: (2016)