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Fluorescent coherent diffractive imaging with accelerating light sheets

delete2019-04-24
delete11
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OA
AI
J
Jeffrey J. Field *
J
Jeff Squier
R
Randy A. Bartels
DOI:10.1364/OE.27.013015delete
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Abstract

Abstract

En 中文
Fluorescence microscopy is a powerful method for producing high fidelity images with high spatial resolution, particularly in the biological sciences. We recently introduced coherent holographic image reconstruction by phase transfer (CHIRPT), a single-pixel imaging method that significantly improves the depth of field in fluorescence microscopy and enables holographic refocusing of fluorescent light. Here we demonstrate that by installing a confocal slit conjugate to the illuminating light sheets used in CHIRPT, out-of-focus light is rejected, thus improving lateral spatial resolution and rejecting noise from out-of-focus fluorescent light. Confocal CHIRPT is demonstrated and fully modeled. Finally, we explore the use of beam shaping and point-spread-function engineering to enable holographic single-lens light-sheet microscopy with single-pixel detection. (C) 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
Keywords:
MICROSCOPY
RECONSTRUCTION

Journal

Optics Express cover
Optics Express
IF:
3.3
Papers:
6.1W
Citations:
14.3W

Organization

C
Colorado State University System
Scholars:
1.3W
Papers: 1.0W
Citations: 3
C
colorado state university fort collins
Scholars:
8.1K
Papers: 6.1K
Citations: 2