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        <parTitl xml:lang="en">Immunofluorescence data of 700 host cell proteins in Sars-CoV2 infected vs non-infected VeroE6 cells</parTitl>
        <IDNo agency="SND">doi-10-17044-scilifelab-14315777-0</IDNo>
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        <parTitl xml:lang="en">Immunofluorescence data of 700 host cell proteins in Sars-CoV2 infected vs non-infected VeroE6 cells</parTitl>
        <IDNo agency="SND">doi-10-17044-scilifelab-14315777-0</IDNo>
        <IDNo agency="DOI">https://doi.org/10.17044/SCILIFELAB.14315777</IDNo>
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        <AuthEnty xml:lang="en" affiliation="Science for Life Laboratory">Ouyang, Wei</AuthEnty>
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        <distDate xml:lang="en" date="2022-02-17" />
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      <abstract xml:lang="en" contentType="abstract">The data set contains ≈ 75,000 confocal images of mixed Vero E6 cell populations (SARS-CoV2 infected vs non-infected). Cells had been infected with the virus for 1 h and fixed 24 hour post infection in 96 well plates. Using immunofluorescence (4 colours) cells were stained for the SARS-CoV2 virus (red), the endoplasmic reticulum (yellow) and nucleus (blue) – same for all images in the data set and used as reference markers. On top of this, 700 different target proteins were stained – one per well (green). Images were acquired with an Opera Phoenix microscope at 63X, using 9 FoV and 3 z-planes per protein target. IN the original study, intensity differences and spatial re-distribution of the target proteins were evaluated in infected vs the non-infected cells. The image resource was generated and described in detail in this research article: (to be added).</abstract>
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