<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Christian Gabriel</submitter><species>Homo sapiens (human)</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BSST631</full_dataset_link><repository>bioimages</repository><figure_sub>Organization</figure_sub><pubmed_authors>Christian Gabriel</pubmed_authors></additional><is_claimable>false</is_claimable><name>24h time series of  U-2 OS knock-in cells expressing fluorescent fusion proteins of CRY1 and/or PER2, left untreated or after shRNA mediated knock-down of either CRY1 or PER2, respectively.</name><description>U-2 OS knock-in cells were genereated using CRISPR to express CRY1 and/or PER2 fused to either mScarlet-I or mClover3 from the endogenous promoter. Cells were either left untreated or trasnduced with lentivirus expressing shRNA against either PER2 or CRY1 (pGIPZ clones V2LHS_172866 (CRY1) V2LHS_52938 (PER2) with mutated tGFP).
Cells were synchronized by washing them in cold PBS. Imging was performed on a Nikon widefield microscope for 24 h with an sampling interval of 1/h, starting 2.5 h after synchronization. Files are .nd2 and contain 4 channels:(1)RFP channel, (2)YFP channel, (3) a YFP/RFP channel (not used) (4) DIC channel. All files are stacks with 24 timepoints. nd2 file image stacks can be opened using the freeware Fiji/ImageJ, but also contain alot of metadata. For each cell line a</description><dates><release>2021-04-18T00:00:00Z</release><modification>2023-04-08T18:54:17.898Z</modification><creation>2021-04-18T19:59:51Z</creation></dates><accession>S-BSST631</accession><cross_references/></HashMap>