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Sample GSM816008 Query DataSets for GSM816008
Status Public on Nov 09, 2012
Title Cord blood CD4+_Act_48h_rep2
Sample type RNA
 
Source name human cord blood CD4+ cell, activated, 48h
Organism Homo sapiens
Characteristics cell type: CD4+ Th cell, cord blood
Treatment protocol Cells were activated on 24-well plates, 4x10^6 cells/ml Yssel´s medium, through the T cell receptor (plate bound antiCD3 500 ng/well, and soluble antiCD28 500 ng/ml, Immunotech, France). To induce Th1 polarization, IL-12 (2.5ng/ml, R&D Systems) was added. To induce Th2 polarization, both IL-4 (10ng/ml, R&D Systems) and anti-IL-12 (10µg/ml, R&D Systems) were added. At 48h timepoint IL-2 (17ng/ml, R&D Systems) was added to the culturing medium. Cells were harvested at 0.5, 1, 2, 4, 6, 12, 24, 48 and 72 h. Naive cells without any treatments were collected as 0h controls from every replicate.
Growth protocol Umbilical cord blood was collected from healthy neonates born in Turku University Hospital, Hospital District of Southwest Finland. Mononuclear cells were isolated with Ficoll-Paque (Amersham Biosciences) gradient centrifugation, and CD4+ cell population was purified using magnetic beads (Dynal CD4 Positive Isolation Kit, Invitrogen) according to manufacturers instructions.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with RNeasy mini kit (Qiagen) according to manufacturers instructions. In-column DNase (RNase-Free Dnase Set, Qiagen) treatment was performed for 15 minutes. RNA was eluted in dH2O.
Label biotin
Label protocol Amplification was started from 100 ng of total RNA using the Affymetrix Two-Cycle cDNA Synthesis Kit (P/N 900432), and cDNA/cRNA synthesis reactions and sample cleanup steps were performed according to Affymetrix´s GeneChip Expression Analysis Technical Manual.
 
Hybridization protocol 15 ug of biotinylated and fragmented cRNA was hybridized to Affymetrix GeneChip Human Genome U133 Plus 2.0 arrays overnight (16-18 hours) at 45*C. GeneChips were washed and stained in the Affymetrix Fluidics Station.
Scan protocol GeneChips were scanned using the GeneChip Scanner 3000 with AutoLoader.
Description biological replicate 2
Data processing The raw microarray data were processed using robust multi-array average normalization and log2-transformed in R (version 2.12.0) using the Bioconductor affy package (version 1.28.0)
 
Submission date Oct 13, 2011
Last update date Sep 01, 2016
Contact name Tapio Lonnberg
Organization name University of Turku
Street address P.O.Box 123
City Turku
ZIP/Postal code 20520
Country Finland
 
Platform ID GPL570
Series (1)
GSE32959 An integrative computational systems biology approach identifies differentially regulated dynamic transcriptome signatures which drive the initiation of human T helper cell differentiation
Relations
Reanalysis of GSM450130
Reanalyzed by GSE86362

Data table header descriptions
ID_REF
VALUE RMA normalized PM signal intensity (log2)

Data table
ID_REF VALUE
1007_s_at 6.901639622
1053_at 8.251544351
117_at 4.139856085
121_at 7.858186647
1255_g_at 3.509952988
1294_at 8.274740837
1316_at 4.393515471
1320_at 3.387476508
1405_i_at 4.938450753
1431_at 3.340803917
1438_at 4.486241649
1487_at 6.673191826
1494_f_at 4.568579242
1552256_a_at 6.650417546
1552257_a_at 7.992993681
1552258_at 3.595198232
1552261_at 4.334633327
1552263_at 6.01617437
1552264_a_at 6.750791136
1552266_at 3.004621885

Total number of rows: 54675

Table truncated, full table size 1212 Kbytes.




Supplementary file Size Download File type/resource
GSM816008.CEL.gz 4.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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