<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Daisuke Ono</submitter><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BSST212</full_dataset_link><repository>bioimages</repository><figure_sub>Organization</figure_sub><pubmed_authors>Daisuke Ono</pubmed_authors><pubmed_authors>Ken-ichi Honma</pubmed_authors><pubmed_authors>Sato Honma</pubmed_authors></additional><is_claimable>false</is_claimable><name>Differential roles of AVP and VIP signaling in the postnatal changes of neural networks for coherent circadian rhythms in the SCN</name><description>Cry double deficient (Cry1,2?/?) mice and Vip receptor 2 deficient (Vipr2?/?) mice were bred with PER2::LUC mice carrying a PER2 luciferase reporter. Wild–type (Cry1,2+/+/Vipr2+/+) PER2::LUC transgenic mice on the C57BL/6J background were used as control. For the measurement of PER2::LUC bioluminescence from a cultured SCN slice, mice of 8–16 weeks or 2–5 days old, kept under LD condition, were euthanized between 8:00 and 16:00 by cervical dislocation and decapitated. The brain was rapidly removed and a coronal SCN slice of 150 ?m or 200 ?m was made.
In the co–culture experiment, the SCN slices of 150 ?m thick were obtained from adult mice carrying the PER2::LUC reporter (recipient). The slice was pre-cultured for 3 or 4 days, and then co–cultured with an SCN slice from mice without the re</description><dates><release>2018-11-18T13:27:26Z</release><modification>2023-03-10T17:22:09.845Z</modification><creation>2018-11-15T07:37:34Z</creation></dates><accession>S-BSST212</accession><cross_references/></HashMap>