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Sample GSM570061 Query DataSets for GSM570061
Status Public on Jul 21, 2011
Title Day 1 culture, biological rep3
Sample type RNA
 
Source name Aortic ring culture at day 1
Organism Rattus norvegicus
Characteristics tissue: aortic rings cultured in collagen gels
genotype: Fisher 344
gender: male
age: 1-2 month
Treatment protocol Freshly harvested aortic rings or collagen gels containing aortic rings were washed in PBS, transferred to buffer RLT from the Qiagen RNAEasy kit, and snap frozen in liquid nitrogen.
Growth protocol Four to six individual aortic rings or ring cultures from each timepoint were combined to generate a sample. Ring cultures were grown in serum free EBM medium (Lonza).
Extracted molecule total RNA
Extraction protocol Following pulverization under liquid nitrogen, extraction of total RNA was performed with a microRNA Easy kit from Qiagen according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA was prepared according to standard Affymetrix Whole Transcript Sense Labeling Protocol from 200 ng of total RNA. (GeneChip® Whole Transcript (WT) Sense Target Labeling Assay User Manual, P/N 701880 Rev. 5)
 
Hybridization protocol Following fragmentation, 10ug of cRNA was hybridized for 17 hr at 45 degrees C on Affymetrix Rat Gene 1.0 ST Arrays. GeneChips were washed and stained in the Affymetrix Gene Chip Fluidics Station 450.
Scan protocol Affymetrix Rat Gene 1.0 ST Arrays were scanned using the Affymetrix GeneChip® 3000 scanner.
Description Gene expression data from day 1 aortic ring cultures
Data processing Raw microarray data were processed with Bioconductor (http://www.bioconductor.org/) Probes were normalized with the Robust Multi-Array normalization procedure (Irizarry RA, Gautier L, Cope L, eds. An r package for analyses of affymetrix oligonucleotide arrays. London: Springer; 2003. Parmigiani RIG, Garrett ES, Zeger S, eds. The analysis of gene expression data: Methods and software.) From the normalized data, genes with significant evidence for differential expression were identified using the Bioconductor limma package (Smyth GK. Linear models and empirical bayes methods for assessing differential expression in microarray experiments. Statistical Applications in Genetics and Molecular Biology. 2004;3:3)
 
Submission date Jul 26, 2010
Last update date Jul 21, 2011
Contact name Alfred C Aplin
E-mail(s) aaplin@u.washington.edu
Phone 206-277-1528
Organization name University of Washington
Department Pathology
Street address Box 357470 HSB-UW
City Seattle
State/province WA
ZIP/Postal code 98195
Country USA
 
Platform ID GPL6247
Series (1)
GSE23152 Gene expression during first day of collagen gel culture of rat aortic rings

Data table header descriptions
ID_REF
VALUE RMA signal

Data table
ID_REF VALUE
10701620 2.721735
10701630 1.615909
10701632 2.439413
10701636 2.378364
10701643 1.94359
10701648 2.709559
10701654 3.106669
10701663 6.845062
10701666 2.847478
10701668 3.094654
10701671 2.592798
10701674 2.777
10701679 3.049926
10701684 4.225434
10701689 3.827369
10701691 5.190845
10701697 5.527102
10701699 6.823154
10701709 9.519823
10701714 4.636771

Total number of rows: 27342

Table truncated, full table size 477 Kbytes.




Supplementary file Size Download File type/resource
GSM570061_AA17.CEL.gz 4.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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