Publication:
Continuous wave excitation two-photon fluorescence microscopy

dc.bibliographiccitation.firstpage222
dc.bibliographiccitation.issue3
dc.bibliographiccitation.journalJournal of Microscopy
dc.bibliographiccitation.lastpage225
dc.bibliographiccitation.volume176
dc.contributor.authorHänninen, P. E.
dc.contributor.authorSoini, E.
dc.contributor.authorHell, S. W.
dc.date.accessioned2018-04-23T11:48:27Z
dc.date.available2018-04-23T11:48:27Z
dc.date.issued1994
dc.description.abstractTwo‐photon excitation fluorescence imaging is feasible with continuous wave lasers. Images of biological specimens are obtained by employing photon counting in conjunction with an increased recording time. The approach allows two‐photon three‐dimensional imaging of fluorescently labelled specimens with inexpensive lasers.
dc.identifier.doi10.1111/j.1365-2818.1994.tb03518.x
dc.identifier.gro3142380
dc.identifier.urihttps://resolver.sub.uni-goettingen.de/purl?gro-2/13520
dc.language.isoen
dc.notes.internlifescience updates Crossref Import
dc.notes.statusfinal
dc.relation.issn0022-2720
dc.titleContinuous wave excitation two-photon fluorescence microscopy
dc.typejournal_article
dc.type.internalPublicationunknown
dc.type.peerReviewedno
dspace.entity.typePublication

Files

Collections