4D super-resolution microscopy with conventional fluorophores and single wavelength excitation in optically thick cells and tissues.
<h4>Background</h4>Optical super-resolution imaging of fluorescently stained biological samples is rapidly becoming an important tool to investigate protein distribution at the molecular scale. It is therefore important to develop practical super-resolution methods that allow capturing t...
Enregistré dans:
Auteurs principaux: | David Baddeley, David Crossman, Sabrina Rossberger, Juliette E Cheyne, Johanna M Montgomery, Isuru D Jayasinghe, Christoph Cremer, Mark B Cannell, Christian Soeller |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Public Library of Science (PLoS)
2011
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/275e5a23c994488d9b10d4bad1c78623 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Fast live-cell conventional fluorophore nanoscopy with ImageJ through super-resolution radial fluctuations
par: Nils Gustafsson, et autres
Publié: (2016) -
Multicolor two-photon imaging of endogenous fluorophores in living tissues by wavelength mixing
par: Chiara Stringari, et autres
Publié: (2017) -
Organic Fluorophores for 1064 nm Excited NIR-II Fluorescence Imaging
par: Wenqi Wang, et autres
Publié: (2021) -
Photoregulated fluxional fluorophores for live-cell super-resolution microscopy with no apparent photobleaching
par: Elias A. Halabi, et autres
Publié: (2019) -
Eigen-analysis reveals components supporting super-resolution imaging of blinking fluorophores
par: Krishna Agarwal, et autres
Publié: (2017)