Cargando…
An aco-2::gfp knock-in enables the monitoring of mitochondrial morphology throughout C. elegans lifespan.
We used CRISPR/Cas9 gene editing in C. elegans in order to fluorescently tag endogenous aconitase-2 (ACO-2). ACO-2 is a mitochondrially localized protein, and the aco-2::gfp strain enabled the examination of native mitochondrial morphology in live animals. Here we validate that the aco-2::gfp strain...
Autores principales: | Begelman, David V., Woods, Georgia, Bhaumik, Dipa, Angeli, Suzanne, Foulger, Anna C, Lucanic, Mark, Lan, Jianfeng, Andersen, Julie K., Lithgow, Gordon J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Caltech Library
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315405/ https://www.ncbi.nlm.nih.gov/pubmed/35903774 http://dx.doi.org/10.17912/micropub.biology.000599 |
Ejemplares similares
-
Creation of a functional unc-11/PICALM GFP knock-in by CRISPR
por: Gallegos, Maria, et al.
Publicado: (2021) -
mScarlet and split fluorophore mScarlet resources for plasmid-based CRISPR/Cas9 knock-in in
C. elegans
por: Witten, Gillian, et al.
Publicado: (2023) -
Tracking of centriole inheritance in C. elegans
por: Erpf, Anna C., et al.
Publicado: (2020) -
Fluorescently labeled
Pseudomonas syringae
DC3000 and 1449b wild-type strains constitutively expressing either eGFP, eCFP, or dsRED
por: Rufián, Jose S, et al.
Publicado: (2022) -
DVC interneuron cGAL driver in Caenorhabditis elegans
por: Oh, Jun Young, et al.
Publicado: (2019)