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Illumination Power, Stability, and Linearity Measurements for Confocal and Widefield Microscopes V.2

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dc.contributor.author Gaudreault, Nathalie en_US
dc.contributor.author PODDER, SANTOSH et al. en_US
dc.date.accessioned 2023-03-31T09:43:50Z
dc.date.available 2023-03-31T09:43:50Z
dc.date.issued 2023-03 en_US
dc.identifier.citation Protocols Io en_US
dc.identifier.issn 2473-1838 en_US
dc.identifier.uri dx.doi.org/10.17504/protocols.io.5jyl853ndl2w/v2 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7686
dc.description.abstract To obtain accurate, reproducible, and interpretable data when conducting imaging experiments, it is critical to consider external factors affecting data acquisition at various steps of the experimental workflow. Illumination power and stability represent two critical factors, especially when comparing fluorescence intensities between images during a time-lapse experiment or experiments performed at different times or on different microscopes. The fluorescence signal can be generated by different types of light sources. These light sources and their coupling elements (e.g., fibers) can display varying performances over time as they age, move, or as environmental conditions change. Unfortunately, microscope users can often only set illumination power as a percentage of its maximal output and may, therefore, not be aware of potential performance changes. It is important to recognize that a set percentage will not always yield the same illumination power in Watts at the objective over the course of an experiment, not to mention between days or systems. This means that selecting for example 10% output may lead to different experimental results over time or even between two microscopes of the same model. In addition to illumination stability, working within the linear range of the illumination power allows to adjust accurately the illumination power absolute value (in mW) using fraction (or %) of its maximal value through the imaging software. If you are responsible for system maintenance, routinely measuring the illumination power, stability, and linearity over time can help you detect issues that affect the integrity of the system and thus the reproducibility of an experiment. This protocol describes how to measure the stability and linearity of the illumination power using calibrated external power sensors. This protocol is at the moment intended for confocal systems (raster scanning and spinning disks), and widefield systems. It represents the collective experience of over 50 imaging scientists. Measurements made by our working group with this protocol are available in a public database, which will be updated with further contributions from the community. en_US
dc.language.iso en en_US
dc.publisher QUAREP en_US
dc.subject Biology en_US
dc.subject 2023-MAR-WEEK4 en_US
dc.subject TOC-MAR-2023 en_US
dc.subject 2023 en_US
dc.title Illumination Power, Stability, and Linearity Measurements for Confocal and Widefield Microscopes V.2 en_US
dc.type Article en_US
dc.contributor.department Dept. of Biology en_US
dc.identifier.sourcetitle Protocols Io en_US
dc.publication.originofpublisher Foreign en_US


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