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Sample GSM1337404 Query DataSets for GSM1337404
Status Public on Mar 01, 2014
Title pDC from donor 1 - 4h Aspergillus infected
Sample type RNA
 
Source name pDC from donor 1- 4h Aspergillus infected
Organism Homo sapiens
Characteristics tissue: blood
Growth protocol A. fumigatus conidia (2 x 105) were plated in 48-well plates and grown in pDC medium to hyphae of 10-20 μm average length. pDCs (2 x 105) were then added to the hyphae in a final volume of 300 μl pDC medium for 2 and 4 hr at 37°C. Unstimulated and -CpG-stimulated pDCs were incubated for 2h and 4h, respectively
Extracted molecule total RNA
Extraction protocol The total RNA was extracted with the RNeasy Mini Kit (Qiagen, Hilden, Germany). The quantity of total RNA was measured with a spectrophotometer at 260 nanometers, and the RNA integrity was assessed using an RNA 6000 Nano LabChip Kit on an Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA, U.S.A.)
Label biotin
Label protocol Total RNA (80-500 ng) was reverse transcribed and the single stranded cDNA was amplified using the Ambion WT Expression Kit (Life Technologies, Inc.). The purified cDNA (5.5 μg) was subsequently fragmented and labeled using the GeneChip WT Terminal Labeling Kit (Affymetrix Inc., Santa Clara, CA, U.S.A.)
 
Hybridization protocol Labeled cDNA (3.5 ug) was then hybridized to the GeneChip Human Gene 2.0 ST array (Affymetrix, Inc.) using the GeneChip Hybridization Oven 640 (Affymetrix, Inc.) at 60 rotations per minute at 45°C for 16-18 hours. After hybridization, the arrays were washed and stained according to the Affymetrix protocol using a GeneChip Fluidics Station 450 (Affymetrix)
Scan protocol The arrays were scanned using the GeneChip Scanner 3000 (Affymetrix).
Data processing The data were analyzed using Express Console and Transcriptome Analysis Console (TAC) software (Affymetrix, Inc.). The regulated genes were calculated by dividing the linear intensity value found for each probe from experimental groups (2 or 4 hr of pDC-A. fumigatus interaction and CpG stimulated pDCs) by the linear intensity value found for each probe from the control group (unstimulated pDCs). We considered 1.7 linear fold changes the cut-off to classify the down-regulated and up-regulated genes
 
Submission date Feb 28, 2014
Last update date Mar 01, 2014
Contact name Flavio V Loures
E-mail(s) loures@icb.usp.br
Organization name Universidade de Sao Paulo
Department Immunology
Street address Rua Deputado joaquim libanio, 216
City Sao Paulo
State/province SP
ZIP/Postal code 04120090
Country Brazil
 
Platform ID GPL16686
Series (1)
GSE55467 Expression data from pDC infected with Aspergillus fumigatus

Data table header descriptions
ID_REF
VALUE rma-gene-full

Data table
ID_REF VALUE
16650001 2.69256
16650003 3.79704
16650005 4.52366
16650007 3.75821
16650009 2.36225
16650011 3.5124
16650013 5.27571
16650015 3.58712
16650017 3.07358
16650019 3.88462
16650021 5.39163
16650023 3.94007
16650025 5.59039
16650027 2.72906
16650029 4.85407
16650031 5.88506
16650033 2.83513
16650035 2.44302
16650037 2.44409
16650041 6.6763

Total number of rows: 53617

Table truncated, full table size 884 Kbytes.




Supplementary file Size Download File type/resource
GSM1337404_Exp_1_-_4h_HuGene-2_0-st_.CEL.gz 8.7 Mb (ftp)(http) CEL
GSM1337404_Exp_1_-_4h_HuGene-2_0-st_.rma-gene-full.chp.gz 324.7 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file
Processed data are available on Series record

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