NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM983107 Query DataSets for GSM983107
Status Public on Dec 08, 2012
Title Human iDC stimulated with IL-8, replicate 2
Sample type RNA
 
Source name Human iDC_IL-8
Organism Homo sapiens
Characteristics tissue source: peripheral blood mononuclear cells
responder cells: immature dendritic cells (iDCs)
stimulated with: 1 mg/l human recombinant IL-8
Treatment protocol On day 7 iDCs were either left without stimulation (2 control samples) or stimulated with 1 mg/l human recombinant IL-8 (2 IL-8 samples) or with recombinant Brugia malayi AsnRS (2 samples rBmAsnRS). After 48 hours, cells were harvested, pelleted and frozen at -86*C (in TRIzol) for RNA extraction.
Growth protocol Human immature dendritic cells (iDCs) were generated from CD14+ cells isolated from human peripheral blood mononuclear cells, cultured in 6 well plates for 5 days with 50 ng/ml of IL-4 and GM-CSF (1000 IU/ml).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted and amplified using an Affymetrix two-cycle cDNA synthesis kit (Affymetrix, Santa Clara, CA).
Label biotin
Label protocol cRNA was synthesized, labeled, fragmented, and hybridized to an array in accordance to the Affymetrix GeneChip expression analysis technical manual.
 
Hybridization protocol The GeneChip human genome U133 plus 2.0 array was selected for these studies for its overall comprehensive coverage.
Scan protocol After hybridization, arrays were washed and stained with Affymetrix fluidics protocol FS450_0001 and scanned with a 7G Affymetrix GeneChip Scanner
Description IL8 KRON7124
Data processing Image data were analyzed with Affymetrix Expression Consoleā„¢ software and normalized with Robust Multichip Analysis (RMA; www.bioconductor.org/) to determine signal log ratios. The mean fold change was calculated from the 2 independent biological replicates for each of the 3 experimental conditions (6 arrays total). The statistical significance of differential gene expression and false discovery rates (FDR) were derived through a Rank Product algorithm available as an analysis package in BioConductor (RankProd, www.bioconductor.org/).
 
Submission date Aug 08, 2012
Last update date Dec 08, 2012
Contact name Michael Andrew Kron
E-mail(s) [email protected]
Phone 414 955 5613
Fax 414 955 6568
Organization name Medical College of Wisconsin
Department Medicine
Lab BIotechnology and Bioengineering
Street address 8701 Watertown Plank Road
City Milwaukee
State/province Wisconsin
ZIP/Postal code 53206
Country USA
 
Platform ID GPL570
Series (1)
GSE39999 Filarial nematode AsnRS interacts with interleukin 8 receptors in iDCs but causes different gene expression patterns compared to iDCs stimulated by interleukin 8.

Data table header descriptions
ID_REF
VALUE RMA normalised intensities in log2 scale

Data table
ID_REF VALUE
1007_s_at 7.66502
1053_at 8.83639
117_at 8.29757
121_at 8.91875
1255_g_at 6.27863
1294_at 7.77936
1316_at 5.67097
1320_at 5.00942
1405_i_at 7.72829
1431_at 3.46622
1438_at 5.8048
1487_at 8.17765
1494_f_at 5.72447
1552256_a_at 9.8279
1552257_a_at 7.91397
1552258_at 5.52061
1552261_at 4.37855
1552263_at 8.66264
1552264_a_at 9.45562
1552266_at 3.07986

Total number of rows: 54675

Table truncated, full table size 998 Kbytes.




Supplementary file Size Download File type/resource
GSM983107_KRON_IL-8_52001900911908020113412666987124.CEL.gz 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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