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dc.contributor.authorMandracchia, Biagio
dc.contributor.authorGennari, Oriella
dc.contributor.authorMarchesano, Valentina
dc.contributor.authorPaturzo, Melania
dc.contributor.authorFerraro, Pietro
dc.date.accessioned2026-02-22T19:44:35Z
dc.date.available2026-02-22T19:44:35Z
dc.date.issued2016
dc.identifier.citationJournal of Biophotonics 2017 10, 1163–1170es
dc.identifier.issn1864-063Xes
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/82980
dc.description.abstractThe study of cell adhesion contacts is pivotal to understand cell mechanics and interaction at substrates or chemical and physical stimuli. We designed and built a HoloTIR microscope for label-free quantitative phase imaging of total internal reflection. Here we show for the first time that HoloTIR is a good choice for label-free study of focal contacts and of cell/substrate interaction as its sensitivity is enhanced in comparison with standard TIR microscopy. Finally, the simplicity of implementation and relative low cost, due to the requirement of less optical components, make HoloTIR a reasonable alternative, or even an addition, to TIRF microscopy for mapping cell/substratum topography. As a proof of concept, we studied the formation of focal contacts of fibroblasts on three substrates with different levels of affinity for cell adhesion.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.titleLabel free imaging of cell‐substrate contacts by holographic total internal reflection microscopyes
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1002/jbio.201600177es
dc.identifier.publicationfirstpage1163es
dc.identifier.publicationissue9es
dc.identifier.publicationlastpage1170es
dc.identifier.publicationtitleJournal of Biophotonicses
dc.identifier.publicationvolume10es
dc.peerreviewedSIes
dc.identifier.essn1864-0648es
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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