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Sample GSM1139517 Query DataSets for GSM1139517
Status Public on Jan 01, 2016
Title Mixture, biological rep1
Sample type RNA
 
Source name HepaRG cells treated with the mixture of TCDD and endosulfan for 30 hours
Organism Homo sapiens
Characteristics cell type: HepaRG cells
Treatment protocol DMSO was removed from the medium for twenty-four hours before treating the cells for 30 hours with 25nM TCDD, 10μM alphaendosulfan, the mixture of the two pollutants or the vehicle (0.15% DMSO).
Growth protocol HepaRG were differentiated as described previously except that 1.5% DMSO was used for cell differentiation (Aninat et al. 2006).
Extracted molecule total RNA
Extraction protocol RNA from HepaRG cells (one well from a six-well plate) was prepared using the RNeasy mini kit from Qiagen (France) as described previously (Bui et al. 2009) except that a DNase I step was included in the protocol. For the microarray studies, the quality of the RNA (RIN value) was assessed with a Bionalyzer (Agilent Technologies).
Label biotin
Label protocol ssDNA (sense single stranded DNA) was synthetized using the Affymetrix GeneChip Whole Transcript Sense Target Labelling Assay kit, according to the manufacturer’s protocol. ssDNA samples were then fragmented according to the Affymetrix protocol. The purified ssDNA was quantified and its quality was assessed with a Bioanalyzer. Subsequent labeling of the samples was performed by synthesis of Biotin-labeled ssDNA using the GeneChip WT Terminal Labeling kit (Affymetrix).
 
Hybridization protocol ssDNA targets were hybridized onto high-density microarrays (Affymetrix Human Genome 1.0 ST GeneChip array) according to the Affymetrix Eukaryotic Target manual.The microarrays were then washed and stained using the Affymetrix fluidics station 450/250 and Genechip Operating Software.
Scan protocol The microarrays were scanned with an Affymetrix GeneArray scanner.
Description Gene expression data from HepaRG cells treated with the mixture of TCDD and endosulfan for 30 hours.
Data processing The datasets obtained were processed and normalized using the plier program in R.
 
Submission date May 13, 2013
Last update date Jan 01, 2016
Contact name Lawrence Aggerbeck
E-mail(s) lawrence.aggerbeck@parisdescartes.fr
Organization name INSERM UMR S-747
Street address 45 rue des Saints Peres
City Paris
ZIP/Postal code 75006
Country France
 
Platform ID GPL6244
Series (1)
GSE46874 Effects of Combined Persistant Organic Pollutants on Global Gene Expression in Human HepaRG Cells

Data table header descriptions
ID_REF
VALUE normalized signal intensity

Data table
ID_REF VALUE
7892501 245.412
7892502 41.565
7892503 45.034
7892504 1291.288
7892505 9.804
7892506 16.475
7892507 6.561
7892508 29.429
7892509 4564.578
7892510 27.626
7892511 20.384
7892512 104.941
7892513 24.485
7892514 2781.970
7892515 1107.446
7892516 77.452
7892517 18.660
7892518 8.946
7892519 34.919
7892520 735.481

Total number of rows: 33296

Table truncated, full table size 502 Kbytes.




Supplementary file Size Download File type/resource
GSM1139517_3.4.CEL.gz 4.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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