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Multifocal multiphoton microscopy

Bewersdorf, Jörg, Pick, Rainer, Hell, Stefan W.·1998·Optics Letters

Abstract

We present a real-time, direct-view multiphoton excitation fluorescence microscope that provides three-dimensional imaging at high resolution. Using a rotating microlens disk, we split the near-infrared light of a mode-locked titanium-sapphire laser into an array of beams that are transformed into an array of high-aperture foci at the object. We typically scan at 225 frames per second and image the fluorescence with a camera that reads out the images at video rate. For 1.4 aperture oil and 1.2 water immersion lenses at 780-nm excitation we obtained axial resolutions of 0.84 and 1.4mum , respectively, which are similar to that of a single-beam two-photon microscope. Compared with the latter setup, our system represents a 40-100-fold increase in efficiency, or imaging speed. Moreover, it permits the observation with the eye of high-resolution two-photon images of (live) samples.

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Metadata

Authors
Bewersdorf, J., Pick, R., & Hell, S. W.
Venue
Optics Letters
Published
1998-05-01
Volume
23
Issue
9
Pages
655
ISSN
  • 0146-9592 (ISSN-L)
  • 1539-4794
OpenAlex
W2040723705
Cited by
429
References
0
FWCI
11.89
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Multifocal multiphoton microscopy. https://app.cochat.ai/papers/10.1364/ol.23.000655
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Bewersdorf, J., Pick, R., & Hell, S. W. (1998). Multifocal multiphoton microscopy. Optics Letters. https://doi.org/10.1364/ol.23.000655

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