Literature DB >> 24974025

Quantitative confocal microscopy: beyond a pretty picture.

James Jonkman1, Claire M Brown2, Richard W Cole3.   

Abstract

Quantitative optical microscopy has become the norm, with the confocal laser-scanning microscope being the workhorse of many imaging laboratories. Generating quantitative data requires a greater emphasis on the accurate operation of the microscope itself, along with proper experimental design and adequate controls. The microscope, which is more accurately an imaging system, cannot be treated as a "black box" with the collected data viewed as infallible. There needs to be regularly scheduled performance testing that will ensure that quality data are being generated. This regular testing also allows for the tracking of metrics that can point to issues before they result in instrument malfunction and downtime. In turn, images must be collected in a manner that is quantitative with maximal signal to noise (which can be difficult depending on the application) without data clipping. Images must then be processed to correct for background intensities, fluorophore cross talk, and uneven field illumination. With advanced techniques such as spectral imaging, Förster resonance energy transfer, and fluorescence-lifetime imaging microscopy, experimental design needs to be carefully planned out and include all appropriate controls. Quantitative confocal imaging in all of these contexts and more will be explored within the chapter.
© 2014 Elsevier Inc. All rights reserved.

Keywords:  Confocal; Controls; Morphology; PMT; Performance testing; Protocols; Quantification; Spectral

Mesh:

Year:  2014        PMID: 24974025     DOI: 10.1016/B978-0-12-420138-5.00007-0

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN: 0091-679X            Impact factor:   1.441


  10 in total

1.  Any Way You Slice It-A Comparison of Confocal Microscopy Techniques.

Authors:  James Jonkman; Claire M Brown
Journal:  J Biomol Tech       Date:  2015-07

2.  Advances in Confocal Microscopy and Selected Applications.

Authors:  W Matt Reilly; Christopher J Obara
Journal:  Methods Mol Biol       Date:  2021

3.  A Practical Approach to Quantitative Processing and Analysis of Small Biological Structures by Fluorescent Imaging.

Authors:  Crystal M Noller; Maria Boulina; George McNamara; Angela Szeto; Philip M McCabe; Armando J Mendez
Journal:  J Biomol Tech       Date:  2016-05-13

4.  Semi-blind sparse affine spectral unmixing of autofluorescence-contaminated micrographs.

Authors:  Blair J Rossetti; Steven A Wilbert; Jessica L Mark Welch; Gary G Borisy; James G Nagy
Journal:  Bioinformatics       Date:  2020-02-01       Impact factor: 6.937

Review 5.  Tutorial: guidance for quantitative confocal microscopy.

Authors:  James Jonkman; Claire M Brown; Graham D Wright; Kurt I Anderson; Alison J North
Journal:  Nat Protoc       Date:  2020-03-31       Impact factor: 13.491

6.  Comparison of Multiscale Imaging Methods for Brain Research.

Authors:  Jessica Tröger; Christian Hoischen; Birgit Perner; Shamci Monajembashi; Aurélien Barbotin; Anna Löschberger; Christian Eggeling; Michael M Kessels; Britta Qualmann; Peter Hemmerich
Journal:  Cells       Date:  2020-06-01       Impact factor: 6.600

7.  IntensityCheck - The light measuring app for microscope performance checks and consistent fluorescence imaging.

Authors:  Dirk Dormann
Journal:  PLoS One       Date:  2019-03-28       Impact factor: 3.240

Review 8.  Navigating the Landscape of Tumor Extracellular Vesicle Heterogeneity.

Authors:  Sabrina Roy; Hsing-Ying Lin; Chung-Yu Chou; Chen-Han Huang; Julia Small; Noah Sadik; Caroline M Ayinon; Elizabeth Lansbury; Lilian Cruz; Anudeep Yekula; Pamela S Jones; Leonora Balaj; Bob S Carter
Journal:  Int J Mol Sci       Date:  2019-03-18       Impact factor: 5.923

Review 9.  Recent Advances in Luminescence Imaging of Biological Systems Using Lanthanide(III) Luminescent Complexes.

Authors:  Jorge H S K Monteiro
Journal:  Molecules       Date:  2020-04-29       Impact factor: 4.411

10.  Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward.

Authors:  Elina Nürnberg; Mario Vitacolonna; Julia Klicks; Elena von Molitor; Tiziana Cesetti; Florian Keller; Roman Bruch; Torsten Ertongur-Fauth; Katja Riedel; Paul Scholz; Thorsten Lau; Richard Schneider; Julia Meier; Mathias Hafner; Rüdiger Rudolf
Journal:  Front Mol Biosci       Date:  2020-02-21
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.