Parallel detection experiment of fluorescence confocal microscopy using DMD
Summary Parallel detection of fluorescence confocal microscopy (PDFCM) system based on Digital Micromirror Device (DMD) is reported in this paper in order to realize simultaneous multi‐channel imaging and improve detection speed. DMD is added into PDFCM system, working to take replace of the single...
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Veröffentlicht in: | Scanning 2016-05, Vol.38 (3), p.234-239 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Summary
Parallel detection of fluorescence confocal microscopy (PDFCM) system based on Digital Micromirror Device (DMD) is reported in this paper in order to realize simultaneous multi‐channel imaging and improve detection speed. DMD is added into PDFCM system, working to take replace of the single traditional pinhole in the confocal system, which divides the laser source into multiple excitation beams. The PDFCM imaging system based on DMD is experimentally set up. The multi‐channel image of fluorescence signal of potato cells sample is detected by parallel lateral scanning in order to verify the feasibility of introducing the DMD into fluorescence confocal microscope. In addition, for the purpose of characterizing the microscope, the depth response curve is also acquired. The experimental result shows that in contrast to conventional microscopy, the DMD‐based PDFCM system has higher axial resolution and faster detection speed, which may bring some potential benefits in the biology and medicine analysis. SCANNING 38:234–239, 2016. © 2015 Wiley Periodicals, Inc. |
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ISSN: | 0161-0457 1932-8745 |
DOI: | 10.1002/sca.21265 |