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Sample GSM173007 Query DataSets for GSM173007
Status Public on Mar 08, 2007
Title WT mouse 3_heart_basal
Sample type RNA
 
Source name WT mouse heart under basal conditions
Organism Mus musculus
Characteristics Strain: C57BL/6J
Gender: Male
Age: 2-3 months
Tissue: heart
Extracted molecule total RNA
Extraction protocol Qiagen Fibrous Tissue Midi Kit (mortar and pestle)
Label biotin
Label protocol Refer to the protocols on the McGill University and Genome Quebec Innovation Centre website (http://www.genomequebec.mcgill.ca/services/microarray.php?page=tech).
 
Hybridization protocol Refer to the protocols on the McGill University and Genome Quebec Innovation Centre website (http://www.genomequebec.mcgill.ca/services/microarray.php?page=tech).
Scan protocol Refer to the protocols on the McGill University and Genome Quebec Innovation Centre website (http://www.genomequebec.mcgill.ca/services/microarray.php?page=tech). An Affymetrix GeneChIP 3000 scanner was used.
Description All hybridization were performed at the McGill University and Genome Quebec Innovation Centre. Affymetrix array technology involves the in-situ synthesis of hundreds of thousands of distinct oligonucleotide sequences onto a glass array using photolithography and combinatorial chemistry. Each 25-mer oligonucleotide is represented by millions of copies in a specific area. Each transcriptional sequence is spanned by 11-20 pairs of oligonucleotide probes randomly spaced throughout the array. All sequences designed on the array are selected from GenBank, dbEST and RefSeq. Target RNA is reverse transcribed into cDNA and in-vitro transcription is performed to generate biotin-labeled cRNA for subsequent hybridization. Hybridized target cRNA is stained with streptavidin phycoerythrin and arrays are scanned using a GeneArray Scanner at an excitation wavelength of 488nm. Light emissions at 570nm are proportional to the bound target at each oligonucleotides position on the GeneChip® array.
Data processing The signal intensities shown in the VALUE column are a measure of abundance of transcript and calculated from combined, background adjusted perfect match and mismatched values of the probe set. The raw data is in MAS 5.0 format.
 
Submission date Mar 05, 2007
Last update date Aug 28, 2018
Contact name Vincent Giguère
E-mail(s) vincent.giguere@mcgill.ca
Phone 514-398-5899
Organization name McGill University
Department Goodman Cancer Centre
Street address 1160 Pine Ave West, McIntyre Bldg Room 710
City Montréal
State/province QC
ZIP/Postal code H3A 1A3
Country Canada
 
Platform ID GPL1261
Series (1)
GSE7196 Differential gene expression between WT and ERRa-null hearts
Relations
Reanalyzed by GSE119085

Data table header descriptions
ID_REF
VALUE signal associated with the probes
DETECTION P-VALUE p-value
ABS_CALL type of absorbance for each probe

Data table
ID_REF VALUE DETECTION P-VALUE ABS_CALL
1415670_at 150.3 0.000244 P
1415671_at 278.7 0.000244 P
1415672_at 390.4 0.000732 P
1415673_at 38.7 0.001953 P
1415674_a_at 143.9 0.000244 P
1415675_at 58.5 0.000244 P
1415676_a_at 636.1 0.000244 P
1415677_at 138.1 0.000244 P
1415678_at 576.9 0.000244 P
1415679_at 443.2 0.000732 P
1415680_at 183.2 0.023926 P
1415681_at 383.7 0.000244 P
1415682_at 80 0.000732 P
1415683_at 474.3 0.000244 P
1415684_at 90.9 0.000244 P
1415685_at 302.3 0.000244 P
1415686_at 220.6 0.000244 P
1415687_a_at 1514.5 0.000244 P
1415688_at 568.7 0.000244 P
1415689_s_at 43.2 0.001221 P

Total number of rows: 45099

Table truncated, full table size 1178 Kbytes.




Supplementary file Size Download File type/resource
GSM173007.CEL.gz 5.7 Mb (ftp)(http) CEL

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