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Proceedings Paper

Time-resolved 3D confocal fluorescence microscopy on living cells
Author(s): M. Schellenberg; E. Peev; M. Kloster; J. Napier; W. Neu
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Paper Abstract

Time resolved 3D-microscopy using DMD-arrays utilizes the principles of confocal microscopy. Application fitted patterns optimize optical imaging of reflective, transparent, and fluorescent objects. High spatial resolution is achieved simultaneously with high temporal resolution due to fast DMD control. This enables to visualize and track processes in vivo within living biocells.

Paper Details

Date Published: 25 November 2010
PDF: 9 pages
Proc. SPIE 7376, Laser Applications in Life Sciences, 737612 (25 November 2010); doi: 10.1117/12.871459
Show Author Affiliations
M. Schellenberg, Univ. of Applied Sciences Emden/Leer (Germany)
E. Peev, Univ. of Applied Sciences Emden/Leer (Germany)
M. Kloster, Univ. of Applied Sciences Emden/Leer (Germany)
J. Napier, Univ. of Applied Sciences Emden/Leer (Germany)
W. Neu, Univ. of Applied Sciences Emden/Leer (Germany)


Published in SPIE Proceedings Vol. 7376:
Laser Applications in Life Sciences
Matti Kinnunen; Risto Myllylä, Editor(s)

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