Volumetric imaging of fluorescently labeled BPAE cells
Using the Nanoimager-S microscope (ONI, Oxford Nanoimaging) with a sCMOS sensor (Hamamatsu, ORCA-Flash4.0 V2), FluoCells™ Prepared Slide #1 (Thermo, #F36924) were imaged with a 100X, 1.4 NA, oil-immersion objective (Olympus). DAPI, Alexa-488 and MitoTracker™ Red excitation was delivered by 405 nm, 4...
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ftzenodo:oai:zenodo.org:6865066 2024-09-15T18:28:53+00:00 Volumetric imaging of fluorescently labeled BPAE cells Víctor Abonza 2022-07-20 https://doi.org/10.5281/zenodo.6865066 unknown Zenodo https://doi.org/10.5281/zenodo.6836636 https://doi.org/10.21203/rs.3.rs-984659/v1 https://doi.org/10.1101/2021.10.17.464398 https://doi.org/10.5281/zenodo.6865065 https://doi.org/10.5281/zenodo.6865066 oai:zenodo.org:6865066 info:eu-repo/semantics/openAccess Creative Commons Attribution 4.0 International https://creativecommons.org/licenses/by/4.0/legalcode info:eu-repo/semantics/other 2022 ftzenodo https://doi.org/10.5281/zenodo.686506610.5281/zenodo.683663610.21203/rs.3.rs-984659/v110.1101/2021.10.17.46439810.5281/zenodo.6865065 2024-07-26T05:24:41Z Using the Nanoimager-S microscope (ONI, Oxford Nanoimaging) with a sCMOS sensor (Hamamatsu, ORCA-Flash4.0 V2), FluoCells™ Prepared Slide #1 (Thermo, #F36924) were imaged with a 100X, 1.4 NA, oil-immersion objective (Olympus). DAPI, Alexa-488 and MitoTracker™ Red excitation was delivered by 405 nm, 473 nm and 561 nm lasers, respectively. Light was collected while using two emission filters (1: 525/50; 2: Band 1 575-616.5) and a Channel Splitter dichroic 561 LP. A 3D Z-stack of the sample was acquired for each channel. 22 frames were generated, each separated 50 nm from each other in Z. Other/Unknown Material Orca Zenodo |
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Using the Nanoimager-S microscope (ONI, Oxford Nanoimaging) with a sCMOS sensor (Hamamatsu, ORCA-Flash4.0 V2), FluoCells™ Prepared Slide #1 (Thermo, #F36924) were imaged with a 100X, 1.4 NA, oil-immersion objective (Olympus). DAPI, Alexa-488 and MitoTracker™ Red excitation was delivered by 405 nm, 473 nm and 561 nm lasers, respectively. Light was collected while using two emission filters (1: 525/50; 2: Band 1 575-616.5) and a Channel Splitter dichroic 561 LP. A 3D Z-stack of the sample was acquired for each channel. 22 frames were generated, each separated 50 nm from each other in Z. |
format |
Other/Unknown Material |
author |
Víctor Abonza |
spellingShingle |
Víctor Abonza Volumetric imaging of fluorescently labeled BPAE cells |
author_facet |
Víctor Abonza |
author_sort |
Víctor Abonza |
title |
Volumetric imaging of fluorescently labeled BPAE cells |
title_short |
Volumetric imaging of fluorescently labeled BPAE cells |
title_full |
Volumetric imaging of fluorescently labeled BPAE cells |
title_fullStr |
Volumetric imaging of fluorescently labeled BPAE cells |
title_full_unstemmed |
Volumetric imaging of fluorescently labeled BPAE cells |
title_sort |
volumetric imaging of fluorescently labeled bpae cells |
publisher |
Zenodo |
publishDate |
2022 |
url |
https://doi.org/10.5281/zenodo.6865066 |
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Orca |
op_relation |
https://doi.org/10.5281/zenodo.6836636 https://doi.org/10.21203/rs.3.rs-984659/v1 https://doi.org/10.1101/2021.10.17.464398 https://doi.org/10.5281/zenodo.6865065 https://doi.org/10.5281/zenodo.6865066 oai:zenodo.org:6865066 |
op_rights |
info:eu-repo/semantics/openAccess Creative Commons Attribution 4.0 International https://creativecommons.org/licenses/by/4.0/legalcode |
op_doi |
https://doi.org/10.5281/zenodo.686506610.5281/zenodo.683663610.21203/rs.3.rs-984659/v110.1101/2021.10.17.46439810.5281/zenodo.6865065 |
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1810470307962552320 |