{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE304nnn/GSE304678/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Transcriptomics"],"species":["Rattus norvegicus"],"gds_type":["Expression profiling by high throughput sequencing"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE304678"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"Cytokine-signaling single cell Seq","description":"The design of this experiment was to identify early response genes after exposure to a cytokine associated with tissue resident macrophages. The highly glucose responsive insulinoma cell line (832/13) was subcloned from INS-1 cells, a cell line derived from rat beta-cells. 832/13 cells were used as the experimental model. The design wase exposure of 832/13 cells to either no treatment or 1ng/mL IL-1b for 3 h. At the end of the 3h period, the 832/13 cells were removed from monolayer culture and placed into a single cell suspension for library construction.","dates":{"publication":"2026/09/23"},"accession":"GSE304678","cross_references":{"GSM":["GSM9155156","GSM9155158","GSM9155157"],"GPL":["20084"],"GSE":["304678"],"taxon":["Rattus norvegicus"],"PMID":["[42572286]"]}}