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Part 1: Document Description
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Citation |
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Title: |
Replication data for: Fluorescence fluctuation-based super-resolution microscopy using multimodal waveguided illumination |
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Identification Number: |
doi:10.18710/JEN4SB |
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Distributor: |
DataverseNO |
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Date of Distribution: |
2021-05-27 |
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Version: |
1 |
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Bibliographic Citation: |
Opstad, Ida S., 2021, "Replication data for: Fluorescence fluctuation-based super-resolution microscopy using multimodal waveguided illumination", https://doi.org/10.18710/JEN4SB, DataverseNO, V1 |
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Citation |
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Title: |
Replication data for: Fluorescence fluctuation-based super-resolution microscopy using multimodal waveguided illumination |
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Identification Number: |
doi:10.18710/JEN4SB |
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Authoring Entity: |
Opstad, Ida S. (UiT The Arctic University of Norway) |
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Other identifications and acknowledgements: |
Hansen, Daniel H. |
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Producer: |
UiT The Arctic University of Norway |
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Date of Production: |
2020-09-04 |
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Grant Number: |
UiT strategic funding |
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Grant Number: |
301401 |
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Grant Number: |
749666 |
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Grant Number: |
836355 |
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Distributor: |
DataverseNO |
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Distributor: |
UiT The Arctic University of Norway |
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Access Authority: |
Opstad, Ida S. |
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Depositor: |
Opstad, Ida Sundvor |
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Date of Deposit: |
2021-03-01 |
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Holdings Information: |
https://doi.org/10.18710/JEN4SB |
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Study Scope |
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Keywords: |
Medicine, Health and Life Sciences, Physics, TIRF, waveguide imaging, fluctuation imaging, super-resolution, actin, salmon keratocytes, fluctuation imaging, chip microscopy |
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Abstract: |
<p>The chip-based total internal reflection fluorescence microscopy data is of fixed salmon keratocytes labelled using phalloidin-ATTO647N and acquired using 660 nm excitation, 10X 0.3NA water dipping objective.</p> <p></p> <p>Abstract of publication: Photonic chip-based total internal reflection fluorescence microscopy (c-TIRFM) is an emerging technology enabling a large TIRF excitation area decoupled from the detection objective. Additionally, due to the inherent multimodal nature of wide waveguides, it is a convenient platform for introducing temporal fluctuations in the illumination pattern. The fluorescence fluctuation-based nanoscopy technique Multiple Signal Classification Algorithm (MUSICAL) does not assume stochastic independence of the emitter emission and can therefore exploit fluctuations arising from other sources, as such multimodal illumination patterns. In this work, we demonstrate and verify the utilization of fluctuations in the illumination for super-resolution imaging using MUSICAL on actin in salmon keratocytes. The resolution improvement was measured to be 2.2–3.6-fold compared to the corresponding conventional images. DHH built the imaging system and contributed in the data acquisition</p> |
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Date of Collection: |
2020-09-04-2020-09-04 |
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Country: |
Norway |
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Geographic Coverage: |
Troms, Tromsø |
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Kind of Data: |
Experimental |
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Methodology and Processing |
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Sources Statement |
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Data Access |
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Other Study Description Materials |
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Related Publications |
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Citation |
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Title: |
Ida S. Opstad, Daniel H. Hansen, Sebastian Acuña, Florian Ströhl, Anish Priyadarshi, Jean-Claude Tinguely, Firehun T. Dullo, Roy A. Dalmo, Tore Seternes, Balpreet S. Ahluwalia, and Krishna Agarwal, "Fluorescence fluctuation-based super-resolution microscopy using multimodal waveguided illumination," Opt. Express 29, 23368-23380 (2021) |
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Identification Number: |
10.1364/OE.423809 |
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Bibliographic Citation: |
Ida S. Opstad, Daniel H. Hansen, Sebastian Acuña, Florian Ströhl, Anish Priyadarshi, Jean-Claude Tinguely, Firehun T. Dullo, Roy A. Dalmo, Tore Seternes, Balpreet S. Ahluwalia, and Krishna Agarwal, "Fluorescence fluctuation-based super-resolution microscopy using multimodal waveguided illumination," Opt. Express 29, 23368-23380 (2021) |
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Label: |
0_ReadMe.txt |
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Notes: |
text/plain |
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Label: |
waveguide_600um_step_200nm.zip |
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Text: |
16-bit TIFF stack |
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Notes: |
application/zip |