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Sample GSM1141226 Query DataSets for GSM1141226
Status Public on Aug 05, 2013
Title peripheral blood T-cells of with newly diagnosed ITP 3
Sample type RNA
 
Source name peripheral blood T-cells of with newly diagnosed ITP
Organism Homo sapiens
Characteristics disease state: newly diagnosed ITP
tissue: peripheral blood
cell type: T-cell
Treatment protocol Cells were snap frozen in -80 C. Heparin anti-coagulated blood was obtained from each study subject. T-cells were isolated, in brief, peripheral blood mononuclear cells (PBMCs) were separated from the blood immediately after collection, by density gradient centrifugation. After removal of CD14+ cells by magnetic microbeads, T-cells were positively selected using CD3+ magnetic microbeads, according to the manufacturer's recommendations (MACS, Miltenyi Biotec, Surrey, UK).
Extracted molecule total RNA
Extraction protocol Total RNA was prepared using Chomczynski's method (Anal Biochem 162, 156-9 (1987))
Label Biotin
Label protocol Twenty ng of purified RNA was reverse transcribed, amplified and labeled using the Ovation amplification system V2 (NuGEN Technologies Inc, San Carlos, CA) according to the manufacturer's instructions. Five μg of the generated cDNA was fragmented and biotinylated using the Encore biotin module (NuGEN).
 
Hybridization protocol Following fragmentation, 5 ug of cRNA were hybridized for 16 hr at 45C on Human U133 Plus 2.0 arrays. Arrays were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol After hybridisation (according to the Minimum Information About a Microarray Experiment guideline), the arrays were scanned using an Affymetrix confocal laser scanner (Affymetrix, GeneArray scanner GCS3000) and visualised using GeneChip Operating Software (GCOS, Affymetrix).
Description gene expression data from T-cell
Data processing The raw expression signals were preprocessed following the method ofMASS5 (Affymetrix).The robust quantile method was applied to get normalized expression values
 
Submission date May 14, 2013
Last update date Aug 05, 2013
Contact name Intawat Nookaew
E-mail(s) [email protected]
Organization name University of Arkansas for Medical Sciences
Department Department of Biomedical Informatics
Street address 4301 W Markham St
City Little Rock
ZIP/Postal code 72205
Country USA
 
Platform ID GPL570
Series (1)
GSE46922 Differences in gene expression and cytokines levels between newly diagnosed and chronic pediatric immune thrombocytopenia (ITP)

Data table header descriptions
ID_REF
VALUE normalized expression values

Data table
ID_REF VALUE
1569849_at 20
1565661_x_at 7
243389_at 1
1563160_at 2
1563013_at 10
217428_s_at 25
237638_at 1
208354_s_at 7
207053_at 2
224333_s_at 3260
203093_s_at 77
216778_s_at 2
204590_x_at 1797
203295_s_at 3
214427_at 774
241986_at 26
242178_at 11
206290_s_at 2
216018_at 6
222035_s_at 2855

Total number of rows: 54675

Table truncated, full table size 757 Kbytes.




Supplementary file Size Download File type/resource
GSM1141226_New3.CEL.gz 3.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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