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dc.contributor.authorOpstad, Ida Sundvor
dc.contributor.authorStröhl, Florian
dc.contributor.authorFantham, Marcus J.
dc.contributor.authorHockings, Colin
dc.contributor.authorVanderpoorten, Oliver
dc.contributor.authorTartwijk, Francesca W. van
dc.contributor.authorQiaojin Lin, Julie
dc.contributor.authorTinguely, Jean-Claude
dc.contributor.authorDullo, Firehun Tsige
dc.contributor.authorKaminski‐Schierle, Gabriele S.
dc.contributor.authorAhluwalia, Balpreet Singh
dc.contributor.authorKaminski, Clemens F.
dc.date.accessioned2020-03-31T12:41:02Z
dc.date.available2020-03-31T12:41:02Z
dc.date.issued2020-02-17
dc.description.abstractLarge fields of view (FOVs) in total internal reflection fluorescence microscopy (TIRFM) via waveguides have been shown to be highly beneficial for single molecule localisation microscopy on fixed cells [1,2] and have also been demonstrated for short‐term live‐imaging of robust cell types [3‐5], but not yet for delicate primary neurons nor over extended periods of time. Here, we present a waveguide‐based TIRFM set‐up for live‐cell imaging of demanding samples. Using the developed microscope, referred to as <i>the ChipScope</i>, we demonstrate successful culturing and imaging of fibroblasts, primary rat hippocampal neurons and axons of <i>Xenopus</i> retinal ganglion cells (RGCs). The high contrast and gentle illumination mode provided by TIRFM coupled with the exceptionally large excitation areas and superior illumination homogeneity offered by photonic waveguides have potential for a wide application span in neuroscience applications.en_US
dc.identifier.citationOpstad IS, Ströhl F, Fantham MJ, Hockings, Vanderpoorten O, Tartwijk, Qiaojin Lin, Tinguely J, Dullo FT, Kaminski‐Schierle, Ahluwalia BS, Kaminski CF. A waveguide imaging platform for live-cell TIRF imaging of neurons over large fields of view. Journal of Biophotonics. 2020en_US
dc.identifier.cristinIDFRIDAID 1797313
dc.identifier.doihttps://doi.org/10.1002/jbio.201960222
dc.identifier.issn1864-063X
dc.identifier.issn1864-0648
dc.identifier.urihttps://hdl.handle.net/10037/17943
dc.language.isoengen_US
dc.publisherWiley-VCH Verlagen_US
dc.relation.ispartofOpstad, I.S. (2021). Bringing optical nanoscopy to life - Super-resolution microscopy of living cells. (Doctoral thesis). <a href=https://hdl.handle.net/10037/20306>https://hdl.handle.net/10037/20306</a>
dc.relation.journalJournal of Biophotonics
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020-EU.1.3.2./836355/EU/Boosting the resolution of label-free microscopy will put mitochondria in focus more naturally/MitoQuant/en_US
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7-IDEAS-ERC/336716/EU/High-speed chip-based nanoscopy to discover real-time sub-cellular dynamics/NANOSCOPY/en_US
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2020 The Author(s)en_US
dc.subjectVDP::Mathematics and natural science: 400en_US
dc.subjectVDP::Matematikk og Naturvitenskap: 400en_US
dc.titleA waveguide imaging platform for live-cell TIRF imaging of neurons over large fields of viewen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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