Micro-stepping extended focus reduces photobleaching and preserves structured illumination super-resolution features.
Extended focus
Long-term live-cell imaging
Microscopy
Photobleaching
Rapid projections
Super-resolution
Well-defined sectioning
Journal
Journal of cell science
ISSN: 1477-9137
Titre abrégé: J Cell Sci
Pays: England
ID NLM: 0052457
Informations de publication
Date de publication:
27 05 2020
27 05 2020
Historique:
received:
18
10
2019
accepted:
24
03
2020
pubmed:
9
4
2020
medline:
22
6
2021
entrez:
9
4
2020
Statut:
epublish
Résumé
Despite progress made in confocal microscopy, even fast systems still have insufficient temporal resolution for detailed live-cell volume imaging, such as tracking rapid movement of membrane vesicles in three-dimensional space. Depending on the shortfall, this may result in undersampling and/or motion artifacts that ultimately limit the quality of the imaging data. By sacrificing detailed information in the
Identifiants
pubmed: 32265275
pii: jcs.240796
doi: 10.1242/jcs.240796
pii:
doi:
Substances chimiques
Fluorescent Dyes
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Commentaires et corrections
Type : ErratumIn
Informations de copyright
© 2020. Published by The Company of Biologists Ltd.
Déclaration de conflit d'intérêts
Competing interestsThe authors have filed a patent with Inven2 (DOFI 19087) and Dehns (ref. 12.147289) regarding the hardware implementation.