<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter/><species>Homo sapiens (human)</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BIAD1038</full_dataset_link><repository>bioimages</repository><figure_sub>Protocols</figure_sub><figure_sub>Study Component</figure_sub><figure_sub>organisation</figure_sub><figure_sub>Study Protocols</figure_sub><pubmed_authors>Christian Gabriel</pubmed_authors></additional><is_claimable>false</is_claimable><name>Circadian Imaging of PER and CRY Proteins in U-2 OS cells</name><description>U-2 OS knock-in cells were genereated using CRISPR to express CRY1, CRY2, PER1 PER2 fused to either mScarlet-I or mClover3 from the endogenous promoter. All cells were transduced with H2B-iRFP using lentivirus to allow segmentation and tracking of nuclei. 

Additionally, cells were transduced with lentivirus expressing shRNA against either FBXL3 (pGIPZ V2LHS_254986) or a nontargeted control shRNA. 

===Raw Data===

==Dataset Dex==
Cells of selected clones were imaged for ~3days after synchronization with dexamethasone (1µM, 20min) at an imaging interval of 1 picture per hour
==Dataset CHX/Main==
In 3 experiments, cells were imaged for 68 hours with an imaging interval of 1 picture per hour.
After 44-48 hours, 20 µg/ml CHX was added to a subset of cells to inhibit protein production.
For as</description><dates><release>2024-02-09T00:00:00Z</release><modification>2024-02-09T08:55:41.507Z</modification><creation>2024-02-09T08:55:41.507Z</creation></dates><accession>S-BIAD1038</accession><cross_references/></HashMap>