NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM983110 Query DataSets for GSM983110
Status Public on Dec 08, 2012
Title Human iDC control no stimulation, replicate 1
Sample type RNA
 
Source name Human iDC control_no stimulation
Organism Homo sapiens
Characteristics tissue source: peripheral blood mononuclear cells
responder cells: immature dendritic cells (iDCs)
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 Ctrl KRON14
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 7.66816
1053_at 8.82664
117_at 8.55236
121_at 9.05422
1255_g_at 6.2768
1294_at 7.8831
1316_at 5.00022
1320_at 5.11461
1405_i_at 7.57303
1431_at 3.4522
1438_at 5.79958
1487_at 8.22684
1494_f_at 5.61066
1552256_a_at 10.0305
1552257_a_at 7.85308
1552258_at 5.53232
1552261_at 4.8679
1552263_at 8.93323
1552264_a_at 9.38341
1552266_at 3.11128

Total number of rows: 54675

Table truncated, full table size 998 Kbytes.




Supplementary file Size Download File type/resource
GSM983110_14_KRON_1_control_4-13-11.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