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Sample GSM1722624 Query DataSets for GSM1722624
Status Public on Jul 07, 2015
Title ifn_total_1
Sample type RNA
 
Source name WISH cells
Organism Homo sapiens
Characteristics cell line: WISH
rna type: total
treatment: ifn
replicate: 1
Treatment protocol WISH cells were trypsinized and plated in 10cm tissue culture dishes at 4 X 10^6 cells/dish. After 30 hrs, cells were re-fed with fresh medium with or without IFN  (100pM) and/or mTOR inhibitors at saturating concentrations (rapamycin 100nM or Torin1 1M) for 12h.
Growth protocol WISH cells were cultured as previously described [Francois-Newton V, Livingstone M, Payelle-Brogard B, Uze G, Pellegrini S (2012) USP18 establishes the transcriptional and anti-proliferative interferon alpha/beta differential. Biochem J 446: 509-516 and Marijanovic Z, Ragimbeau J, van der Heyden J, Uze G, Pellegrini S (2007) Comparable potency of IFNalpha2 and IFNbeta on immediate JAK/STAT activation but differential down-regulation of IFNAR2. Biochem J 407: 141-151]. WISH cells were obtained from G. Uzé (CNRS, Montpellier) and originate from ATCC (CCL-25). Their identity was compared to HeLa S3 cells by short tandem repeat (STR) loci profiling. This analysis, performed by IdentiCell (Department of Molecular Medicine, Aarhus University Hospital), showed that the two cell lines have identical STR profiles.
Extracted molecule total RNA
Extraction protocol RNAeasy (Qiagen)
Label Biotin
Label protocol Single round labeling recommended by manufacturer.
 
Hybridization protocol Samples were hybridized with the Affymetrix Human Gene 1.1 ST Array according the instructions of the manufacturer
Scan protocol Arrays were scanned using the GeneArray Scanner 3000 according to the instructions from the manufacturer.
Description WISH cells were starved followed by treatment with dmso or with interferon in the presence of dmso, rapamycin or torin-1
Data processing Data were extracted and normalized using a custom CDF and Robust Multi-array Average (RMA) in R (r-project.org) with default settings.
 
Submission date Jun 25, 2015
Last update date Jul 07, 2015
Contact name Ola Larsson
E-mail(s) ola.larsson@ki.se
Phone +46 (0)8 517 73280
Organization name Karolinska Institutet
Department Department of oncology-pathology
Street address CCK, R8:01
City Stockholm
ZIP/Postal code 171 76
Country Sweden
 
Platform ID GPL18190
Series (1)
GSE70270 Assessment of mTOR-Dependent Translational Regulation of Interferon Stimulated Genes

Data table header descriptions
ID_REF
VALUE Log2 RMA signal

Data table
ID_REF VALUE
100009676_at 6.980034959
10000_at 4.466800757
10001_at 9.003538477
10002_at 5.344023477
100033413_at 5.676031092
100033414_at 5.479627513
100033416_at 6.934759754
100033418_at 6.332159853
100033420_at 7.321541639
100033422_at 4.002999886
100033423_at 5.292744668
100033424_at 4.141801005
100033425_at 5.904186859
100033426_at 10.65637098
100033427_at 11.45933354
100033428_at 3.876277137
100033430_at 5.731377383
100033431_at 9.323030119
100033432_at 6.782751063
100033433_at 5.465313968

Total number of rows: 19682

Table truncated, full table size 400 Kbytes.




Supplementary file Size Download File type/resource
GSM1722624_EX30_ARN0013_s1h1_G05_hGene.CEL.gz 4.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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