NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1145391 Query DataSets for GSM1145391
Status Public on Feb 03, 2014
Title Donor D, time 48 h
Sample type RNA
 
Source name primary human monocytes stimulated with CCL2 for 2 h plus LPS for 12 h plus TNF-α for 11 h plus IFN-γ for 7 h; washed and stimulated with IL-10 for 10 h; washed and stimulated with TGF-β for 12 h
Organism Homo sapiens
Characteristics cell type: deactivated monocytes
group: treated
Treatment protocol The human primary blood monocytes were exposed in culture to sequential changes of microenvironmental conditions (chemokines and cytokines, temperature, bacterial-derived molecules, etc.) for 48 h.
Growth protocol Human monocytes were obtained from buffy coats of healthy donors by isolating PBMC on Ficoll-Paque PLUS gradients and subsequent separation with Monocyte Isolation kit II. Monocytes were cultured in RPMI 1640+Glutamax-I Medium (GIBCO, Life Technologies) with 5% human AB serum, and gentamicine.
Extracted molecule total RNA
Extraction protocol Extraction of total RNA was performed using Qiagen miRNeasy kit (Qiagen) according to the manufacturer’s protocol
Label biotin
Label protocol Biotinylated cRNA was prepared using GeneChip® 3’ IVT Express kit according to manufacturer's intructions
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome HG-U133 Plus 2.0 arrays. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol Standard Affymetrix scanning procedures on a GCS3000 7G Affymetrix scanner operated by GCOS, GeneChip Operating Software
Description Gene expression data from Donor D, time 48h
Data processing RMA of .CEL files using affy Bioconductor library. In RMA, PM values have been background adjusted, normalized using quantile normalization, and expression measure calculated using median polish summarization
 
Submission date May 21, 2013
Last update date Feb 03, 2014
Contact name Silvio Bicciato
E-mail(s) silvio.bicciato@unipd.it
Phone +39-049-827-6108
Organization name University of Padova
Department Molecular Medicine
Street address via U. Bassi 59/b
City Padova
ZIP/Postal code 35131
Country Italy
 
Platform ID GPL17180
Series (1)
GSE47122 Transcriptomic profiling of the development of the inflammatory response in human monocytes in vitro

Data table header descriptions
ID_REF
VALUE RMA-calculated signal intensity (log2)

Data table
ID_REF VALUE
GC00U902522_at 2.87273967
GC00U902726_at 3.060506718
GC00U902727_at 4.364344534
GC00U902728_at 2.388001665
GC00U905129_at 3.455404404
GC00U913730_at 4.729523764
GC00U916295_at 4.489138124
GC00U921637_at 5.529706131
GC00U921664_at 2.889949038
GC00U921668_at 4.014095859
GC00U921857_at 4.410190935
GC00U922209_at 5.104483647
GC00U922231_at 3.027036292
GC00U922298_at 2.531322764
GC00U922307_at 2.714648562
GC00U922384_at 4.613445935
GC00U922430_at 3.791123437
GC00U922457_at 4.889089757
GC00U922633_at 4.275976709
GC00U922796_at 4.158275511

Total number of rows: 18862

Table truncated, full table size 495 Kbytes.




Supplementary file Size Download File type/resource
GSM1145391_D_48h.CEL.gz 4.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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