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Sample GSM570069 Query DataSets for GSM570069
Status Public on Jul 21, 2011
Title TNF treated collagen culture, biological rep1
Sample type RNA
 
Source name TNF treated collagen gel culture of aortic ring, day 2
Organism Rattus norvegicus
Characteristics treatment: TNF treated collagen
tissue: aortic rings cultured in collagen gels
genotype: Fisher 344
gender: male
age: 1-2 month old rat aortas
Treatment protocol Collagen or fibrin 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 ring cultures from each treatment groupd were combined to generate a sample. All cultures were grown in serum free EBM medium (Lonza). Samples were divided into treatment groups receiving 10ng/ml recombinant Rat TNFa or left untreated.
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 in TNF treated collagen gel cultures or rat aorta at day 2
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)
GSE23153 Gene expression in TNF treated rat aortic rings cultured in collagen or fibrin gels.

Data table header descriptions
ID_REF
VALUE RMA signal

Data table
ID_REF VALUE
10701620 3.3209
10701630 2.059451
10701632 2.740418
10701636 1.917582
10701643 2.008489
10701648 3.25298
10701654 2.934995
10701663 6.638639
10701666 2.246011
10701668 3.302715
10701671 2.596373
10701674 2.628906
10701679 3.89968
10701684 4.574542
10701689 3.449519
10701691 4.888515
10701697 5.532384
10701699 7.083638
10701709 9.503496
10701714 4.584047

Total number of rows: 27342

Table truncated, full table size 477 Kbytes.




Supplementary file Size Download File type/resource
GSM570069_Col_TNF_GL8.CEL.gz 4.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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