Cargando…
Protocol to image and quantify nuclear pore complexes using high-resolution laser scanning confocal microscopy
Nuclear pore complexes are pathways for nuclear-cytoplasmic communication that participate in chromatin organization. Here, we present a protocol to image and quantify the number of nuclear pore complexes in cells. We describe steps for cell plating and culture, immunofluorescence detection, and con...
Autores principales: | Mich-Basso, Jocelyn D., Kühn, Bernhard |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495640/ https://www.ncbi.nlm.nih.gov/pubmed/37651236 http://dx.doi.org/10.1016/j.xpro.2023.102552 |
Ejemplares similares
-
A protocol to quantify chromatin compaction with confocal and super-resolution microscopy in cultured cells
por: Martin, Laura, et al.
Publicado: (2021) -
Protocol for imaging nuclear pore complexes on isolated nuclei of zebrafish early embryos by field emission scanning electron microscopy
por: Shen, Weimin, et al.
Publicado: (2023) -
Immuno-Electron and Confocal Laser Scanning Microscopy of the Glycocalyx
por: Twamley, Shailey Gale, et al.
Publicado: (2021) -
Correlative confocal and scanning electron microscopy of cultured cells without using dedicated equipment
por: Casares-Arias, Javier, et al.
Publicado: (2021) -
Iris ultrastructure in patients with synechiae as revealed by in vivo laser scanning confocal microscopy: In vivo iris ultrastructure in patients with Synechiae by Laser Scanning Confocal Microscopy
por: Li, Ming, et al.
Publicado: (2016)