NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE153790 Query DataSets for GSE153790
Status Public on Jul 05, 2020
Title Gene expression analysis of mouse ID8 ovarian cancer cells stimulated with CCL6 in vitro
Organism Mus musculus
Experiment type Expression profiling by array
Summary We used mouse Clariom-S microarrays to study the gene expression profile of ID8 cancer cells stimulated with C-C Chemokine Ligand 6 (CCL6).
 
Overall design RNA extracted from ID8 mouse ovarian cancer cell lines (n=3) and ID8 cells stimulated with 200ng/mL CCL6 for 6 hours (n=3) was hybridized on Affymetrix Mouse Clariom S microarrays. We sought to identify key regulatory pathways activated in ovarian cancer cells upon stimulation with CCL6 that play a role in migration and metastasis. To understand the signaling mechanism of CCR1-CCL6 interaction in ovarian cancer, we generated biological replicates for unstimulated ID8 cells and ID8 cells stimulated with 200ng/mL CCL6 for 6 hours.
 
Contributor(s) Dorigo O
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Jul 04, 2020
Last update date Jul 08, 2020
Contact name Oliver Dorigo
Organization name Stanford University
Street address 300 Pasteur Dr
City Stanford
ZIP/Postal code 94304
Country USA
 
Platforms (1)
GPL23038 [Clariom_S_Mouse] Affymetrix Clariom S Assay, Mouse (Includes Pico Assay)
Samples (6)
GSM4654093 ID8-unstimulated, biological rep1
GSM4654094 ID8-unstimulated, biological rep2
GSM4654095 ID8-unstimulated, biological rep3
Relations
BioProject PRJNA644103

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE153790_RAW.tar 6.4 Mb (http)(custom) TAR (of CEL)
Raw data provided as supplementary file
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap