NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1145396 Query DataSets for GSM1145396
Status Public on Feb 03, 2014
Title Donor L, 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 L, 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 3.035442232
GC00U902726_at 3.193125905
GC00U902727_at 4.577757465
GC00U902728_at 2.609630082
GC00U905129_at 3.475972766
GC00U913730_at 6.111868041
GC00U916295_at 4.567877789
GC00U921637_at 5.762244809
GC00U921664_at 3.0890406
GC00U921668_at 4.061643685
GC00U921857_at 4.588262092
GC00U922209_at 5.488462042
GC00U922231_at 3.049329475
GC00U922298_at 2.641740843
GC00U922307_at 2.651194613
GC00U922384_at 4.701534274
GC00U922430_at 3.912969373
GC00U922457_at 4.875342522
GC00U922633_at 4.164576467
GC00U922796_at 4.652210967

Total number of rows: 18862

Table truncated, full table size 495 Kbytes.




Supplementary file Size Download File type/resource
GSM1145396_L_48h.CEL.gz 4.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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