Literature DB >> 17760615

A white light confocal microscope for spectrally resolved multidimensional imaging.

J H Frank1, A D Elder, J Swartling, A R Venkitaraman, A D Jeyasekharan, C F Kaminski.   

Abstract

Spectrofluorometric imaging microscopy is demonstrated in a confocal microscope using a supercontinuum laser as an excitation source and a custom-built prism spectrometer for detection. This microscope system provides confocal imaging with spectrally resolved fluorescence excitation and detection from 450 to 700 nm. The supercontinuum laser provides a broad spectrum light source and is coupled with an acousto-optic tunable filter to provide continuously tunable fluorescence excitation with a 1-nm bandwidth. Eight different excitation wavelengths can be simultaneously selected. The prism spectrometer provides spectrally resolved detection with sensitivity comparable to a standard confocal system. This new microscope system enables optimal access to a multitude of fluorophores and provides fluorescence excitation and emission spectra for each location in a 3D confocal image. The speed of the spectral scans is suitable for spectrofluorometric imaging of live cells. Effects of chromatic aberration are modest and do not significantly limit the spatial resolution of the confocal measurements.

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Mesh:

Year:  2007        PMID: 17760615     DOI: 10.1111/j.1365-2818.2007.01803.x

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


  20 in total

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Authors:  Winsome Cheung; Michael Gill; Alessandro Esposito; Clemens F Kaminski; Nathalie Courousse; Serge Chwetzoff; Germain Trugnan; Nandita Keshavan; Andrew Lever; Ulrich Desselberger
Journal:  J Virol       Date:  2010-03-24       Impact factor: 5.103

2.  Lenslet array tunable snapshot imaging spectrometer (LATIS) for hyperspectral fluorescence microscopy.

Authors:  Jason G Dwight; Tomasz S Tkaczyk
Journal:  Biomed Opt Express       Date:  2017-02-28       Impact factor: 3.732

3.  Dual-color three-dimensional STED microscopy with a single high-repetition-rate laser.

Authors:  Kyu Young Han; Taekjip Ha
Journal:  Opt Lett       Date:  2015-06-01       Impact factor: 3.776

4.  Hyperspectral imaging microscopy for identification and quantitative analysis of fluorescently-labeled cells in highly autofluorescent tissue.

Authors:  Silas J Leavesley; Naga Annamdevula; John Boni; Samantha Stocker; Kristin Grant; Boris Troyanovsky; Thomas C Rich; Diego F Alvarez
Journal:  J Biophotonics       Date:  2011-10-11       Impact factor: 3.207

5.  Supercontinuum white light lasers for flow cytometry.

Authors:  William G Telford; Fedor V Subach; Vladislav V Verkhusha
Journal:  Cytometry A       Date:  2009-05       Impact factor: 4.355

6.  Ultraviolet-visible non-supercontinuum ultrafast source enabled by switching single silicon strand-like photonic crystal fibers.

Authors:  Haohua Tu; Stephen A Boppart
Journal:  Opt Express       Date:  2009-09-28       Impact factor: 3.894

7.  A FRET sensor for non-invasive imaging of amyloid formation in vivo.

Authors:  Gabriele S Kaminski Schierle; Carlos W Bertoncini; Fiona T S Chan; Annemieke T van der Goot; Stefanie Schwedler; Jeremy Skepper; Simon Schlachter; Tjakko van Ham; Alessandro Esposito; Janet R Kumita; Ellen A A Nollen; Christopher M Dobson; Clemens F Kaminski
Journal:  Chemphyschem       Date:  2011-02-09       Impact factor: 3.102

8.  Protein amyloids develop an intrinsic fluorescence signature during aggregation.

Authors:  Fiona T S Chan; Gabriele S Kaminski Schierle; Janet R Kumita; Carlos W Bertoncini; Christopher M Dobson; Clemens F Kaminski
Journal:  Analyst       Date:  2013-02-18       Impact factor: 4.616

9.  Lifetime imaging of a fluorescent protein sensor reveals surprising stability of ER thiol redox.

Authors:  Edward Avezov; Benedict C S Cross; Gabriele S Kaminski Schierle; Mikael Winters; Heather P Harding; Eduardo Pinho Melo; Clemens F Kaminski; David Ron
Journal:  J Cell Biol       Date:  2013-04-15       Impact factor: 10.539

10.  FRET imaging of hemoglobin concentration in Plasmodium falciparum-infected red cells.

Authors:  Alessandro Esposito; Teresa Tiffert; Jakob M A Mauritz; Simon Schlachter; Lawrence H Bannister; Clemens F Kaminski; Virgilio L Lew
Journal:  PLoS One       Date:  2008-11-21       Impact factor: 3.240

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