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Sample GSM525149 Query DataSets for GSM525149
Status Public on Sep 01, 2010
Title Animal 11
Sample type RNA
 
Source name Left ventricle, sham surgery, saturated fat diet
Organism Rattus norvegicus
Characteristics strain: Wistar
gender: male
tissue: left ventricle
surgery: sham
coronary status: normal
diet: high saturated fat
Treatment protocol Rats were randomly assigned to receive either a sham-operation (SH) or coronary ligation to induce cardiac dysfunction (HF). Following surgery, rats were immediately fed either a normal rodent chow (NC) or a high saturated fat chow (SAT) with 60% caloric content derived from fat (25% palmitic, 33% stearic, 33% oleic acid, Research Diets).
Growth protocol Tissue from a separate set of animals (n=6/group) was quick frozen in liquid nitrogen for microarray analysis.
Extracted molecule total RNA
Extraction protocol RNA was extracted from all tissues using a standard protocol and Tri-reagent.
Label Cy3
Label protocol Total RNA was converted to cDNA by reverse transcription using Superscript II reverse transcriptase and T7-(dT)24 primers, followed by second-strand synthesis to generate double-stranded cDNA.
 
Hybridization protocol A total of 0.75 micrograms of biotin-labeled cRNA was applied to a BeadChip and allowed to hybridize overnight at 55°C for approximately 18 hours, followed by washing and staining with streptavidin-Cy3 prior to visualization.
Scan protocol BeadChips were visualized using the BeadStation scanner, which uses a dual-laser confocal scanner with 0.8 µm resolution to determine fluorescence values for each bead on the chip.
Description Approximately 22,000 RefSeq and EST transcripts are present on the arrays in the form of oligo-coated (50mer) beads.
INF11_SHAM_SAT
Data processing After scanning the probe arrays, the resulting images were analyzed using the BeadStudio software (V3, Illumina, Inc., San Diego, CA), which calculates the mean fluorescence signal across all replicates of each gene/transcript, along with a probability that the mean signal for each gene/transcript on the chip is greater than background (i.e., detection p-value). Both non-normalized and normalized (quantile) data were generated for each sample.
 
Submission date Mar 23, 2010
Last update date Mar 23, 2010
Contact name Molly Bray Bray
E-mail(s) mbray@uab.edu
Phone 205-975-7651
Fax 205-934-8665
Organization name Univ of Alabama at Birmingham
Department Genetics
Lab KAUL-406
Street address 720 20th Street S
City Birmingham
State/province AL
ZIP/Postal code 35294
Country USA
 
Platform ID GPL10239
Series (1)
GSE21021 Myocardial contractile response to physiological stress improves with high saturated fat feeding in heart failure

Data table header descriptions
ID_REF
VALUE Normalized signal intensity
Detection Pval Detection p-value

Data table
ID_REF VALUE Detection Pval
1 125.7793 0.3951515
2 117.3172 0.5878788
3 176.9378 0.01939394
4 120.216 0.510303
5 112.2578 0.6957576
6 125.7425 0.3951515
7 133.0556 0.2654545
8 129.3155 0.3272727
9 114.0058 0.659394
10 100.2268 0.9272727
11 111.6647 0.7127272
12 106.8865 0.8157576
13 205.6367 0.00969697
14 127.2944 0.36
15 156.3735 0.05818182
16 139.1609 0.1709091
17 163.9451 0.03878788
18 124.3911 0.420606
19 86.98407 0.9915152
20 108.9141 0.769697

Total number of rows: 22517

Table truncated, full table size 515 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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