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Sample GSM236935 Query DataSets for GSM236935
Status Public on Apr 06, 2010
Title CD45+/Sca1+_BM_rep1
Sample type RNA
 
Source name CD45+/Sca1+ cells isolated from the bone marrow
Organism Mus musculus
Characteristics Strain: C57BL/6, Age: 6-8 weeks old, Tissue: bone marrow
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using RNeasy Micro Kit (Qiagen, Valencia, CA) following the protocol supplied by the manufacturer. Disposable RNA chips (Agilent RNA 6000 Nano LabChip kit, Agilent Technologies, Waldbrunn, Germany) were used to determine the concentration and purity/integrity of RNA samples using Agilent 2100 Bioanalyzer.
Label biotin
Label protocol One-cycle target labeling assays were performed, using Affymetrix standard protocols (Affymetrix, Santa Clara,CA). Briefly, biotin-labeled target synthesis was performed, starting from 1 µg of total cellular RNA, according to the protocol supplied by the manufacturer (Affymetrix, Santa Clara, CA). Labeled cRNA was purified using Affymetrix GeneChip Sample Cleanup Module and fragmented (20 µg) as described in the Affymetrix GeneChip protocol. Disposable RNA chips (Agilent RNA 6000 Nano LabChip kit, Agilent Technologies, Waldbrunn, Germany) and Agilent 2100 Bioanalyzer were used to determine the cRNA concentration/quality as well as to optimize the cRNA fragmentation.
 
Hybridization protocol The fragmented cRNA was then hybridized to an identical lot of Affymetrix Mouse430A GeneChip arrays for 16 hours. GeneChips were washed and stained using the instrument’s standard Eukaryotic GE WS2v4 protocol, using antibody-mediated signal amplification.
Scan protocol GeneChip were finally scanned using the Affymetrix GeneChip scanner 3000, enabled for High-Resolution Scanning.
Description Synthesis of biotinylated cRNA targets, arrays hybridization (Mouse430A GeneChip, Affymetrix, Santa Clara,CA), staining and scanning were performed using Affymetrix standard protocols starting from 1μg of total RNA.
Data processing Scaling to TGT value=250. The GeneChip-Operating-Software (GCOS) absolute analysis algorithm was used to determine the mRNA expression levels (Signal), while the GCOS comparison analysis algorithm was used in order to compare gene expression levels between two samples.
 
Submission date Oct 11, 2007
Last update date Aug 14, 2011
Contact name Rossella Manfredini
E-mail(s) manfredini.rossella@unimore.it
Phone +390592058065
Organization name Centre for Regenerative Medicine
Department Life Sciences
Street address Via Gottardi 100
City Modena
ZIP/Postal code 41100
Country Italy
 
Platform ID GPL339
Series (1)
GSE9296 Gene expression profiling of CD45+/Sca1+ cells isolated from the bone marrow and the muscle

Data table header descriptions
ID_REF
VALUE GCOS-calculated signal intensity
ABS_CALL Detection call
DETECTION P-VALUE Detection call p-value

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 111.888 P 0.0032123
AFFX-BioB-M_at 162.02 P 4.42873e-05
AFFX-BioB-3_at 88.4856 P 9.4506e-05
AFFX-BioC-5_at 258.041 P 0.00010954
AFFX-BioC-3_at 198.501 P 8.14279e-05
AFFX-BioDn-5_at 272.781 P 4.42873e-05
AFFX-BioDn-3_at 1408.69 P 5.16732e-05
AFFX-CreX-5_at 1978.64 P 4.42873e-05
AFFX-CreX-3_at 3245.32 P 4.42873e-05
AFFX-DapX-5_at 1.08916 A 0.48511
AFFX-DapX-M_at 4.24898 A 0.41138
AFFX-DapX-3_at 1.87084 A 0.921998
AFFX-LysX-5_at 9.92837 A 0.123572
AFFX-LysX-M_at 3.82313 A 0.804734
AFFX-LysX-3_at 6.55967 A 0.156732
AFFX-PheX-5_at 0.791255 A 0.883887
AFFX-PheX-M_at 1.32708 A 0.794268
AFFX-PheX-3_at 6.61734 A 0.41138
AFFX-ThrX-5_at 7.20446 A 0.60308
AFFX-ThrX-M_at 7.54407 A 0.440646

Total number of rows: 22690

Table truncated, full table size 705 Kbytes.




Supplementary file Size Download File type/resource
GSM236935.CEL.gz 3.5 Mb (ftp)(http) CEL
GSM236935.CHP.gz 6.1 Mb (ftp)(http) CHP
Processed data included within Sample table

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