NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM462630 Query DataSets for GSM462630
Status Public on Dec 17, 2010
Title transcriptional profiling of CD133+ cells in coronary artery disease, SG-42H
Sample type RNA
 
Source name healthy subject
Organism Homo sapiens
Characteristics tissue: peripheral blood
cell type: CD133+ cells
disease: healthy
Treatment protocol Cardivovascular examination and baseline testing were performed after an overnight fast (except for water). Symptom-limited treadmill exercise was performed using the modified Bruce protocal. Healthy subjects of similar age and sex distribution were recruited for the study to serve as controls for baseline analysis.
Growth protocol CAD patients enrolled in a cardiac rehabilitation program consisting of 36 sessions of 60 minutes each, spaced over 3 months. Medical management was stable for at least a month prior to program participation and all patients were maintained on medications throughout the study as prescribed without change in preparation or dose.
Extracted molecule total RNA
Extraction protocol 32 ml of PB was used for isolation of CD133+ cells using fluorescence-actived cell sorting. Total RNA was extracted from CD133+ cells with an RNAqueous micro RNA isolation kit (Ambion, Austin, TX). Cells were lysed in buffer containing guanidinium thiocyanate.
Label biotin
Label protocol Biotin labeled with Affymetrix's IVT labeling kits (Affymetrix, Santa Clara, CA).
 
Hybridization protocol Fragmented RNA was assessed for relative length on Agilent 2100 bioanalyzer and hybridized to Affymetrix HG-U133 Plus 2.0 chips for 16 hours.
Scan protocol Affymetrix GeneChip scanner.
Description CD133+ cells sorted from PB.
SG-42H
Data processing Intensities were pre-processed with MAS5.0, and further processed with variance stablization transformation ('S10'). 26,123 probesets present in at least 2 out of 14 chips (4 healthy controls and 10 CAD baselines) were S10 transformed and analyzed.
 
Submission date Oct 16, 2009
Last update date Dec 17, 2010
Contact name Delong Liu
E-mail(s) [email protected]
Phone 301-451-7129
Organization name NHLBI/NIH
Street address 10 Center Drive
City Bethesda
State/province MD
ZIP/Postal code 20892
Country USA
 
Platform ID GPL570
Series (1)
GSE18608 Transcriptional Profiling of CD133+ Cells in Coronary Artery Disease and Effects of Exercise on Gene Expression

Data table header descriptions
ID_REF
VALUE S10-transformed signal intensity

Data table
ID_REF VALUE
1007_s_at 0.38966327
1053_at 0.24451003
117_at 0.39512626
121_at 0.92276349
1294_at 1.03655869
1316_at 0.70739388
1405_i_at 2.28130037
1487_at 0.3009957
1494_f_at 0.53784708
1552256_a_at 0.58044026
1552257_a_at 0.70417127
1552263_at 1.61219845
1552264_a_at 0.95360538
1552274_at 0.24438161
1552277_a_at 0.15115724
1552283_s_at 0.47359742
1552286_at 0.70954451
1552287_s_at 0.41288296
1552291_at 0.47116672
1552301_a_at 0.65349642

Total number of rows: 26123

Table truncated, full table size 553 Kbytes.




Supplementary file Size Download File type/resource
GSM462630.CEL.gz 3.4 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap