| Literature DB >> 19547456 |
Karsten Bahlmann, Peter T So, Michael Kirber, Robert Reich, Bernard Kosicki, William McGonagle, Karl Bellve.
Abstract
We introduce a multiphoton microscope for high-speed three-dimensional (3D) fluorescence imaging. The system combines parallel illumination by a multifocal multiphoton microscope (MMM) with parallel detection via a segmented high-sensitivity charge-couple device (CCD) camera. The instrument consists of a Ti-sapphire laser illuminating a microlens array that projects 36 foci onto the focal plane. The foci are scanned using a resonance scanner and imaged with a custom-made CCD camera. The MMM increases the imaging speed by parallelizing the illumination; the CCD camera can operate at a frame rate of 1428 Hz while maintaining a low read noise of 11 electrons per pixel by dividing its chip into 16 independent segments for parallelized readout. We image fluorescent specimens at a frame rate of 640 Hz. The calcium wave of fluo3 labeled cardiac myocytes is measured by imaging the spontaneous contraction of the cells in a 0.625 second sequence movie, consisting of 400 single images.Entities:
Year: 2007 PMID: 19547456 DOI: 10.1364/oe.15.010991
Source DB: PubMed Journal: Opt Express ISSN: 1094-4087 Impact factor: 3.894