Please use this identifier to cite or link to this item: https://doi.org/10.1117/12.904115
DC FieldValue
dc.titleLine-scan Focal Modulation Microscopy for rapid imaging of thick biological specimens
dc.contributor.authorChong, S.P.
dc.contributor.authorPant, S.
dc.contributor.authorChen, N.
dc.date.accessioned2014-06-19T08:58:40Z
dc.date.available2014-06-19T08:58:40Z
dc.date.issued2011
dc.identifier.citationChong, S.P., Pant, S., Chen, N. (2011). Line-scan Focal Modulation Microscopy for rapid imaging of thick biological specimens. Proceedings of SPIE - The International Society for Optical Engineering 8311 : -. ScholarBank@NUS Repository. https://doi.org/10.1117/12.904115
dc.identifier.isbn9780819489593
dc.identifier.issn0277786X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/74889
dc.description.abstractIn recent development of fluorescence microscopy, the out-of-focus fluorescence background that arises when imaging deep inside biological tissues is critical in determining the image quality and penetration depth. Focal Modulation Microscopy [1- 3] (FMM) is an emerging single-photon excitation fluorescence microscopy technique that can provide sub-micron spatial resolution for deep imaging of biological tissues mainly by preserving the signal-to-background ratio. Here we report a linescan FMM that enables line-by-line recording [4] at video frame rates (>30 fps) depending on the size of region of interest. © 2011 SPIE-OSA-IEEE.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1117/12.904115
dc.sourceScopus
dc.typeConference Paper
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1117/12.904115
dc.description.sourcetitleProceedings of SPIE - The International Society for Optical Engineering
dc.description.volume8311
dc.description.page-
dc.description.codenPSISD
dc.identifier.isiut000298372300036
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