Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/55486
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dc.contributorDepartment of Electronic and Information Engineering-
dc.creatorTan, HM-
dc.creatorPechprasarn, S-
dc.creatorZhang, J-
dc.creatorPitter, MC-
dc.creatorSomekh, MG-
dc.date.accessioned2016-09-07T02:22:01Z-
dc.date.available2016-09-07T02:22:01Z-
dc.identifier.urihttp://hdl.handle.net/10397/55486-
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.rightsThis work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/en_US
dc.rightsThe following publication Tan, H., Pechprasarn, S., Zhang, J. et al. High Resolution Quantitative Angle-Scanning Widefield Surface Plasmon Microscopy. Sci Rep 6, 20195 (2016) is available at https://dx.doi.org/10.1038/srep20195en_US
dc.titleHigh Resolution Quantitative Angle-Scanning Widefield Surface Plasmon Microscopyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume6-
dc.identifier.doi10.1038/srep20195-
dcterms.abstractWe describe the construction of a prismless widefield surface plasmon microscope; this has been applied to imaging of the interactions of protein and antibodies in aqueous media. The illumination angle of spatially incoherent diffuse laser illumination was controlled with an amplitude spatial light modulator placed in a conjugate back focal plane to allow dynamic control of the illumination angle. Quantitative surface plasmon microscopy images with high spatial resolution were acquired by post-processing a series of images obtained as a function of illumination angle. Experimental results are presented showing spatially and temporally resolved binding of a protein to a ligand. We also show theoretical results calculated by vector diffraction theory that accurately predict the response of the microscope on a spatially varying sample thus allowing proper quantification and interpretation of the experimental results.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationScientific reports, 1 2016, v. 6, no. , p. 1-11-
dcterms.isPartOfScientific reports-
dcterms.issued2016-
dc.identifier.isiWOS:000368986100001-
dc.identifier.scopus2-s2.0-84957558258-
dc.identifier.eissn2045-2322-
dc.identifier.rosgroupid2015005233-
dc.description.ros2015-2016 > Academic research: refereed > Publication in refereed journal-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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