Enhanced photon collection enables four dimensional fluorescence nanoscopy of living systems
Super-resolution microscopy often suffers from low contrast and slow recording times. Here the authors present an optical implementation which makes the fluorescent proteins’ ON–OFF switching cycles more efficient, enhancing contrast and spatio-temporal resolution in 3D cell and tissue imaging.
Enregistré dans:
Auteurs principaux: | Luciano A. Masullo, Andreas Bodén, Francesca Pennacchietti, Giovanna Coceano, Michael Ratz, Ilaria Testa |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Nature Portfolio
2018
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/7cc42c8ba8c447d2a6cf7482a6916e8d |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Smart scanning for low-illumination and fast RESOLFT nanoscopy in vivo
par: Jes Dreier, et autres
Publié: (2019) -
Multi-photon near-infrared emission saturation nanoscopy using upconversion nanoparticles
par: Chaohao Chen, et autres
Publié: (2018) -
Three-dimensional total-internal reflection fluorescence nanoscopy with nanometric axial resolution by photometric localization of single molecules
par: Alan M. Szalai, et autres
Publié: (2021) -
A set of monomeric near-infrared fluorescent proteins for multicolor imaging across scales
par: Mikhail E. Matlashov, et autres
Publié: (2020) -
A transparent waveguide chip for versatile total internal reflection fluorescence-based microscopy and nanoscopy
par: Anish Priyadarshi, et autres
Publié: (2021)