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A simple, inexpensive and multi‐scale 3‐D fluorescent test sample for optical sectioning microscopies

Authors :
Jennifer Corridon
Adi Salomon
Aaron Au
Julien Fernandes
Christopher M. Yip
Thierry Bastien
Ilya Olevsko
Kaitlin Szederkenyi
Brigitte Delhomme
Martin Oheim
Bar-Ilan University [Israël]
Saints-Pères Paris Institute for Neurosciences (SPPIN - UMR 8003)
Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité)
University of Toronto
Biomedtech Facilities (UMS 2009 / US36)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité)
Université Paris Cité (UPCité)
BioImagerie Photonique – Photonic BioImaging (UTechS PBI)
Institut Pasteur [Paris] (IP)
Spectral and Airyscan confocal micrographs were taken on microscopes of the imaging core facility (CNRS UMS 2009, INSERM US 36, BioMedTech Facilities). Marcoscopic light-sheet images were acquired at UtechS Photonic BioImaging (Imagopole), C2RT, Institut Pasteur, supported by the French National Research Agency (France BioImaging
ANR-10-INBS-04
Investments for the Future). AS acknowledges support from the French Ministry of Foreign Affairs and the French Embassy in Tel Aviv (Chateaubriand fellowship). KS is the laureate of a joint CNRS-U Toronto PhD fellowship. This study was financed by the CNRS, the University of Paris, the Israeli Science Foundation (ISF, grant 1231/19), U Toronto and the European Union (H2020 Eureka! Eurostars, 'NanoScale,' E!12848, to MO & AS). The authors are grateful for mobility support from a Franco-Israeli CNRS-LIA, 'ImagiNano,' and the FranceBioImaging large-scale national infrastructure initiative (FBI, ANR-10-INSB-04, Investments for the future).
ANR-10-INBS-0004,France-BioImaging,Développment d'une infrastructure française distribuée coordonnée(2010)
Fernandes, Julien
Développment d'une infrastructure française distribuée coordonnée - - France-BioImaging2010 - ANR-10-INBS-0004 - INBS - VALID
Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP)
Université de Paris (UP)
Institut Pasteur [Paris]
Source :
Microscopy Research and Technique, Microscopy Research and Technique, 2021, ⟨10.1002/jemt.23813⟩, Microscopy Research and Technique, Wiley, 2021, ⟨10.1002/jemt.23813⟩
Publication Year :
2021
Publisher :
HAL CCSD, 2021.

Abstract

Fluorescence standards allow for quality control and for the comparison of data sets across instruments and laboratories in applications of quantitative fluorescence. For example, users of microscopy core facilities expect a homogenous and time-invariant illumination and a uniform detection sensitivity, which are prerequisites for quantitative imaging analysis, particle tracking or fluorometric pH or Ca2+-concentration measurements. Similarly, confirming the three-dimensional (3-D) resolution of optical sectioning micro-scopes prior to volumetric reconstructions calls for a regular calibration with a standardised point source. Typically, the test samples required for such calibration measurements are different ones, and they depend much on the very microscope technique used. Also, the ever-increasing choice among these techniques increases the demand for comparison and metrology across instruments. Here, we advocate and demonstrate the multiple uses of a surprisingly versatile and simple 3-D test sample that can complement existing and much more expensive calibration samples: simple commercial tissue paper labelled with a fluorescent highlighter pen. We provide relevant sample characteristics and show examples ranging from the sub-µm to cm scale, acquired on epifluorescence, confocal, image scanning, two-photon (2P) and light-sheet microscopes.Graphical abstractPyranine-labeled tissue paper, imaged upon 405-nm epifluorescence excitation through a 455LP LP dichroic and 465LP emission filter. Objective ×20/NA0.25. Overlaid are the normalised absorbance (dashed) and emission spectra (through line), respectively. In the present work we show that this “primitive” and inexpensive three-dimensional (3-D) test sample is a surprisingly versatile and powerful tool for quality assessment, comparison across microscopes as well as routine metrology for optical sectioning techniques, both for research labs and imaging core facilities.Research highlights-highlighter-pen marked tissue paper is a surprisingly powerful and versatile test sample for 3-D fluorescence microscopies-standard tissue paper presents features ranging from 400 nm to centimetres-our sample can simultaneously be used for testing intensity, field homogeneity, resolution, optical sectioning and image contrast-it is easy to prepare, versatile, photostable and inexpensive

Details

Language :
English
ISSN :
1059910X and 10970029
Database :
OpenAIRE
Journal :
Microscopy Research and Technique, Microscopy Research and Technique, 2021, ⟨10.1002/jemt.23813⟩, Microscopy Research and Technique, Wiley, 2021, ⟨10.1002/jemt.23813⟩
Accession number :
edsair.doi.dedup.....aa30bc243881ff9a0ba232c2870a9365
Full Text :
https://doi.org/10.1002/jemt.23813⟩