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Sample GSM241203 Query DataSets for GSM241203
Status Public on Nov 07, 2007
Title hMSC_Donor5064L_Passage2_Day7
Sample type RNA
 
Source name Passage 2 human MSC grown for 7 days
Organism Homo sapiens
Characteristics Recovered passage 1 human Multipotent Stromal Cells (MSCs) donor 220R plated at 50 cells/cm2 in complete culture medium (CCM: alpha-MEM, 17% FBS, pen-strep, 2 mM L-glutamine) and grown for 7 days.
Biomaterial provider Tulane University Center for Gene Therapy
Extracted molecule total RNA
Extraction protocol RNAqueous Kit (Ambion)
Label Biotin
Label protocol 5 μg of total RNA was used to synthesize double-stranded cDNA (Superscript Choice System/GIBCO BRL Life Technologies). After synthesis, the double-stranded cDNA was purified by phenol/chloroform extraction (Phase Lock Gel, Eppendorf Scientific) and concentrated by ethanol precipitation. In vitro transcription was used to produce biotin-labeled cRNA (BioArray HighYield RNA Transcription Labeling Kit, Enzo Diagnostics). The biotinylated cRNA was then cleaned (RNAeasy Mini Kit Qiagen) and fragmented with metal induced hydrolysis.
 
Hybridization protocol The biotinylated and fragmented cRNA was hybridized on the HG-U133 Plus 2.0 microarray chips (Affymetrix). After washing, microarray chip was stained with streptavidin-phycoerythrin (Molecular Probes), amplified with biotinylated anti-streptavidin (Vector Laboratories) and stained with streptavidin-phycoerythrin.
Scan protocol The microarray was scanned for fluorescence (GeneChip Scanner 3000, Affymetrix) using the GeneChip Operating software 1.0 (GCOS, Affymetrix).
Description Scale factor: 24.8
Background: 92.1
Noise (RawQ): 2.90
%Present: 40.8
Data processing Data was scaled to the target value of 2500 with GCOS that also recorded intensities for perfect match (PM) and mismatch (MM) oligonucleotides, and determined whether genes were present (P), marginal (M) or absent (A).
 
Submission date Nov 05, 2007
Last update date Aug 28, 2018
Contact name Joni Ylostalo
E-mail(s) [email protected]
Organization name Texas A&M
Department Institute for Regenerative Medicine
Street address 5701 Airport Rd., Module C
City Temple
State/province TX
ZIP/Postal code 76502
Country USA
 
Platform ID GPL570
Series (1)
GSE9520 Transcriptome changes in hMSCs during expansion
Relations
Reanalyzed by GSE20125
Reanalyzed by GSE64985
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE expression value
ABS_CALL defines whether gene is present (P), marginal (M), or absent (A)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 1076.07 P 0.00159257
AFFX-BioB-M_at 1224.67 P 0.00141043
AFFX-BioB-3_at 854.28 A 0.083592
AFFX-BioC-5_at 4081.79 P 6.02111e-05
AFFX-BioC-3_at 4197.86 P 7.00668e-05
AFFX-BioDn-5_at 10721 P 4.42873e-05
AFFX-BioDn-3_at 24721.4 P 6.02111e-05
AFFX-CreX-5_at 60551.9 P 5.16732e-05
AFFX-CreX-3_at 95633.6 P 5.16732e-05
AFFX-DapX-5_at 124.012 A 0.712257
AFFX-DapX-M_at 50.6547 A 0.945802
AFFX-DapX-3_at 84.6234 A 0.937071
AFFX-LysX-5_at 30.1652 A 0.868639
AFFX-LysX-M_at 45.6747 A 0.966323
AFFX-LysX-3_at 70.4271 A 0.814869
AFFX-PheX-5_at 28.239 A 0.996405
AFFX-PheX-M_at 47.7089 A 0.860518
AFFX-PheX-3_at 494.581 A 0.239063
AFFX-ThrX-5_at 48.3538 A 0.937071
AFFX-ThrX-M_at 56.4499 A 0.814869

Total number of rows: 54675

Table truncated, full table size 1628 Kbytes.




Supplementary file Size Download File type/resource
GSM241203.CEL.gz 8.1 Mb (ftp)(http) CEL
GSM241203.CHP.gz 6.4 Mb (ftp)(http) CHP
Processed data provided as supplementary file
Processed data included within Sample table

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