Literature DB >> 22906014

A line scanning confocal fluorescent microscope using a CMOS rolling shutter as an adjustable aperture.

E Mei1, P A Fomitchov, R Graves, M Campion.   

Abstract

Traditional confocal microscopy uses a physical aperture barrier to prevent out-of-focus light from reaching the detector. The physical nature of a conventional aperture limits control over the system confocality. We describe a new line scanning confocal microscope that eliminates a need for a physical aperture by employing a software-controllable rolling shutter on a CMOS camera. A confocal image is obtained by synchronizing motion of the rolling shutter and the laser line scanning over a sample. Confocal resolution of this microscope is adjustable in real time and independently established for each fluorescence channel by changing the rolling shutter width. This technology has been implemented in the IN Cell Analyzer 6000 system by GE Healthcare.
© 2012 The Authors Journal of Microscopy © 2012 Royal Microscopical Society.

Mesh:

Year:  2012        PMID: 22906014     DOI: 10.1111/j.1365-2818.2012.03642.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  10 in total

1.  Dual-slit confocal light sheet microscopy for in vivo whole-brain imaging of zebrafish.

Authors:  Zhe Yang; Li Mei; Fei Xia; Qingming Luo; Ling Fu; Hui Gong
Journal:  Biomed Opt Express       Date:  2015-04-21       Impact factor: 3.732

2.  Line-scanning fiber bundle endomicroscopy with a virtual detector slit.

Authors:  Michael Hughes; Guang-Zhong Yang
Journal:  Biomed Opt Express       Date:  2016-05-18       Impact factor: 3.732

3.  Three-dimensional image cytometer based on widefield structured light microscopy and high-speed remote depth scanning.

Authors:  Heejin Choi; Dushan N Wadduwage; Ting Yuan Tu; Paul Matsudaira; Peter T C So
Journal:  Cytometry A       Date:  2014-10-28       Impact factor: 4.355

4.  Assessing the imaging performance of light sheet microscopies in highly scattering tissues.

Authors:  A K Glaser; Y Wang; J T C Liu
Journal:  Biomed Opt Express       Date:  2016-01-14       Impact factor: 3.732

5.  Reduced motion artifacts and speed improvements in enhanced line-scanning fiber bundle endomicroscopy.

Authors:  Andrew Thrapp; Michael Hughes
Journal:  J Biomed Opt       Date:  2021-05       Impact factor: 3.170

6.  Light sheet theta microscopy for rapid high-resolution imaging of large biological samples.

Authors:  Bianca Migliori; Malika S Datta; Christophe Dupre; Mehmet C Apak; Shoh Asano; Ruixuan Gao; Edward S Boyden; Ola Hermanson; Rafael Yuste; Raju Tomer
Journal:  BMC Biol       Date:  2018-05-29       Impact factor: 7.431

7.  Line-scanning confocal microendoscope for nuclear morphometry imaging.

Authors:  Yubo Tang; Jennifer Carns; Rebecca R Richards-Kortum
Journal:  J Biomed Opt       Date:  2017-11       Impact factor: 3.170

8.  A single-molecule localization microscopy method for tissues reveals nonrandom nuclear pore distribution in Drosophila.

Authors:  Jinmei Cheng; Edward S Allgeyer; Jennifer H Richens; Edo Dzafic; Amandine Palandri; Bohdan Lewków; George Sirinakis; Daniel St Johnston
Journal:  J Cell Sci       Date:  2021-12-16       Impact factor: 5.235

9.  Confocal multiview light-sheet microscopy.

Authors:  Gustavo de Medeiros; Nils Norlin; Stefan Gunther; Marvin Albert; Laura Panavaite; Ulla-Maj Fiuza; Francesca Peri; Takashi Hiiragi; Uros Krzic; Lars Hufnagel
Journal:  Nat Commun       Date:  2015-11-25       Impact factor: 14.919

10.  Automated measurement of fast mitochondrial transport in neurons.

Authors:  Kyle E Miller; Xin-An Liu; Sathyanarayanan V Puthanveettil
Journal:  Front Cell Neurosci       Date:  2015-11-03       Impact factor: 5.505

  10 in total

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