<codeBook xmlns="ddi:codebook:2_5" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="ddi:codebook:2_5 https://ddialliance.org/Specification/DDI-Codebook/2.5/XMLSchema/codebook.xsd" version="2.5"><docDscr><citation><titlStmt><titl>Replication data for: Fluorescence fluctuation-based super-resolution microscopy using multimodal waveguided illumination</titl><IDNo agency="DOI">doi:10.18710/JEN4SB</IDNo></titlStmt><distStmt><distrbtr source="archive">DataverseNO</distrbtr><distDate>2021-05-27</distDate></distStmt><verStmt source="archive"><version date="2023-11-01" type="RELEASED">1</version></verStmt><biblCit>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</biblCit></citation></docDscr><stdyDscr><citation><titlStmt><titl>Replication data for: Fluorescence fluctuation-based super-resolution microscopy using multimodal waveguided illumination</titl><IDNo agency="DOI">doi:10.18710/JEN4SB</IDNo></titlStmt><rspStmt><AuthEnty affiliation="UiT The Arctic University of Norway">Opstad, Ida S.</AuthEnty><othId role="Data Collector">Hansen, Daniel H.</othId></rspStmt><prodStmt><producer abbr="UiT">UiT The Arctic University of Norway</producer><prodDate>2020-09-04</prodDate><prodPlac>Tromsø</prodPlac><grantNo agency="UiT The Arctic University of Norway">UiT strategic funding</grantNo><grantNo agency="The Research Council of Norway">301401</grantNo><grantNo agency="European Research Council">749666</grantNo><grantNo agency="European Research Council">836355</grantNo></prodStmt><distStmt><distrbtr source="archive">DataverseNO</distrbtr><distrbtr affiliation="UiT The Arctic University of Norway" abbr="UiT" URI="https://dataverse.no/dataverse/uit">UiT The Arctic University of Norway</distrbtr><contact affiliation="UiT The Arctic University of Norway" email="ida.s.opstad@uit.no">Opstad, Ida S.</contact><depositr>Opstad, Ida Sundvor</depositr><depDate>2021-03-01</depDate></distStmt><holdings URI="https://doi.org/10.18710/JEN4SB"/></citation><stdyInfo><subject><keyword xml:lang="en">Medicine, Health and Life Sciences</keyword><keyword xml:lang="en">Physics</keyword><keyword>TIRF</keyword><keyword>waveguide imaging</keyword><keyword>fluctuation imaging</keyword><keyword>super-resolution</keyword><keyword>actin</keyword><keyword>salmon keratocytes</keyword><keyword>fluctuation imaging</keyword><keyword>chip microscopy</keyword></subject><abstract date="2021-03-01">&lt;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.&lt;/p>
&lt;p>&lt;/p>
&lt;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&lt;/p></abstract><sumDscr><collDate cycle="P1" event="start" date="2020-09-04">2020-09-04</collDate><collDate cycle="P1" event="end" date="2020-09-04">2020-09-04</collDate><nation>Norway</nation><geogCover>Troms</geogCover><geogCover>Tromsø</geogCover><dataKind>Experimental</dataKind></sumDscr></stdyInfo><method><dataColl><sources/></dataColl><anlyInfo/></method><dataAccs><setAvail/><useStmt/><notes type="DVN:TOU" level="dv">&lt;a href="http://creativecommons.org/publicdomain/zero/1.0">CC0 1.0&lt;/a></notes></dataAccs><othrStdyMat><relPubl><citation><titlStmt><titl>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)</titl><IDNo agency="doi">10.1364/OE.423809</IDNo></titlStmt><biblCit>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)</biblCit></citation><ExtLink URI="https://doi.org/10.1364/OE.423809"/></relPubl></othrStdyMat></stdyDscr><otherMat ID="f100506" URI="https://dataverse.no/api/access/datafile/100506" level="datafile"><labl>0_ReadMe.txt</labl><notes level="file" type="DATAVERSE:CONTENTTYPE" subject="Content/MIME Type">text/plain</notes></otherMat><otherMat ID="f89583" URI="https://dataverse.no/api/access/datafile/89583" level="datafile"><labl>waveguide_600um_step_200nm.zip</labl><txt>16-bit TIFF stack</txt><notes level="file" type="DATAVERSE:CONTENTTYPE" subject="Content/MIME Type">application/zip</notes></otherMat></codeBook>