Please use this identifier to cite or link to this item:
|Title:||Line-scan Focal Modulation Microscopy for rapid imaging of thick biological specimens||Authors:||Chong, S.P.
|Issue Date:||2011||Citation:||Chong, 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||Abstract:||In 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  at video frame rates (>30 fps) depending on the size of region of interest. © 2011 SPIE-OSA-IEEE.||Source Title:||Proceedings of SPIE - The International Society for Optical Engineering||URI:||http://scholarbank.nus.edu.sg/handle/10635/74889||ISBN:||9780819489593||ISSN:||0277786X||DOI:||10.1117/12.904115|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.