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DIRECT, a low-cost system for high-speed, low-noise imaging of fluorescent bio-samples

A targeted imaging system has been developed for applications requiring recording from stationary samples at high spatiotemporal resolutions. It works by illuminating regions of interest in rapid sequence, and recording the signal from the whole field of view onto a single photodetector. It can be i...

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Detalles Bibliográficos
Autores principales: Whiteley, Isabell, Song, Chenchen, Howe, Glenn A., Knöpfel, Thomas, Rowlands, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optica Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278627/
https://www.ncbi.nlm.nih.gov/pubmed/37342684
http://dx.doi.org/10.1364/BOE.486507
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author Whiteley, Isabell
Song, Chenchen
Howe, Glenn A.
Knöpfel, Thomas
Rowlands, Christopher J.
author_facet Whiteley, Isabell
Song, Chenchen
Howe, Glenn A.
Knöpfel, Thomas
Rowlands, Christopher J.
author_sort Whiteley, Isabell
collection PubMed
description A targeted imaging system has been developed for applications requiring recording from stationary samples at high spatiotemporal resolutions. It works by illuminating regions of interest in rapid sequence, and recording the signal from the whole field of view onto a single photodetector. It can be implemented at low cost on an existing microscope without compromising existing functionality. The system is characterized in terms of speed, spatial resolution, and tissue penetration depth, before being used to record individual action potentials from ASAP-3 expressing neurons in an ex vivo mouse brain slice preparation.
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spelling pubmed-102786272023-06-20 DIRECT, a low-cost system for high-speed, low-noise imaging of fluorescent bio-samples Whiteley, Isabell Song, Chenchen Howe, Glenn A. Knöpfel, Thomas Rowlands, Christopher J. Biomed Opt Express Article A targeted imaging system has been developed for applications requiring recording from stationary samples at high spatiotemporal resolutions. It works by illuminating regions of interest in rapid sequence, and recording the signal from the whole field of view onto a single photodetector. It can be implemented at low cost on an existing microscope without compromising existing functionality. The system is characterized in terms of speed, spatial resolution, and tissue penetration depth, before being used to record individual action potentials from ASAP-3 expressing neurons in an ex vivo mouse brain slice preparation. Optica Publishing Group 2023-05-08 /pmc/articles/PMC10278627/ /pubmed/37342684 http://dx.doi.org/10.1364/BOE.486507 Text en Published by Optica Publishing Group under the terms of the Creative Commons Attribution 4.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI. https://creativecommons.org/licenses/by/4.0/https://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Whiteley, Isabell
Song, Chenchen
Howe, Glenn A.
Knöpfel, Thomas
Rowlands, Christopher J.
DIRECT, a low-cost system for high-speed, low-noise imaging of fluorescent bio-samples
title DIRECT, a low-cost system for high-speed, low-noise imaging of fluorescent bio-samples
title_full DIRECT, a low-cost system for high-speed, low-noise imaging of fluorescent bio-samples
title_fullStr DIRECT, a low-cost system for high-speed, low-noise imaging of fluorescent bio-samples
title_full_unstemmed DIRECT, a low-cost system for high-speed, low-noise imaging of fluorescent bio-samples
title_short DIRECT, a low-cost system for high-speed, low-noise imaging of fluorescent bio-samples
title_sort direct, a low-cost system for high-speed, low-noise imaging of fluorescent bio-samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278627/
https://www.ncbi.nlm.nih.gov/pubmed/37342684
http://dx.doi.org/10.1364/BOE.486507
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