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Sample GSM863114 Query DataSets for GSM863114
Status Public on Jan 19, 2012
Title heart male pbs 10 dpi rep2
Sample type RNA
 
Source name male heart 10 days post pbs injection
Organism Mus musculus
Characteristics strain: BALB/C
age: 8-10 weeks
treatment: PBS
gender: Male
time: 10 dpi
tissue: heart
Treatment protocol Mice were treated with either PBS or heart-passaged CVB3 intraperitoneally. Mice were harvested at 10 days post infection and hearts were flash frozen in liquid nitrogen for RNA extraction.
Extracted molecule total RNA
Extraction protocol Hearts were homogenized in 2mL TRIzol according to the manufacturer's protocol. PureLink Micro-to-midi Total RNA purification System was used for extraction and purification of RNA
Label Affymetrix GeneChip Whole Transcript Sense Target Labeling Assay (biotin)
Label protocol RNAs were processed for hybridization to Affymetrix Mouse Gene ST 1.0 microarrays using the Affymetrix GeneChip Whole Transcript Sense Target Labeling Assay, according to manufacturer's recommended protocol. One hundred nanograms of total RNA was amplified.
 
Hybridization protocol Hybridization cocktails were prepared as recommended for arrays of Mini/169 format using reagents in the Affymetrix Hybridization Wash Stain kit. Hybridization mix and fragmented, labeled ST-sscDNA were incubated at 99oC for 2 min and 45oC for 5 min, and then centrifuged at maximum speed for 5 min prior to pipetting into the GeneChips (Affymetrix Mouse Gene ST 1.0). Hybridization was performed at 45oC for 18 hours at 60RPM in the Affymetrix rotisserie hybridization oven. The signal amplification protocol for washing and staining of eukaryotic targets was performed in an automated fluidies station (Affymetrix FS450) using Affymetrix protocol FS450_0001.
Scan protocol Arrays were transferred to a GCS3000 laser scanner with autoloader and 3G upgrade (Affymetrix) and scanned at an emission wavelength of 570nm at 2.5 um resolution
Description Gene expression data of male hearts after a 10 day treatment of PBS
Data processing CEL files were imported and analyzed with the default algorithm workflow RMA-Sketch, which includes RMA background correction, and Sketch-Quantile normalization.
The values recommended by Affymetrix as QC metrics include Positive vs. negative AUC (assessment of sensitivity and specificity), as well as all probeset mean and all probeset relative log expression.
 
Submission date Jan 18, 2012
Last update date Jan 19, 2012
Contact name DeLisa Fairweather
E-mail(s) [email protected]
Phone 4105023644
Fax 4109550116
Organization name Johns Hopkins University
Department Environmental Health Sciences
Lab Fairweather Laboratory
Street address 615 N Wolfe St
City Baltimore
State/province MD
ZIP/Postal code 21205
Country USA
 
Platform ID GPL6246
Series (1)
GSE35182 Sex differences during acute myocarditis against coxsackievirus B3 (CVB3)-induced myocarditis (10 dpi) and chronic myocarditis/dilated cardiomyopathy (DCM) against CVB3-induced myocarditis (90 dpi)

Data table header descriptions
ID_REF
VALUE RMA-Sketch (includes RMA background correction and Sketch-Quantile normalization separately for 10 dpi and 90 dpi datasets)

Data table
ID_REF VALUE
10344614 6.35769
10344616 1.73609
10344618 2.10171
10344620 3.23804
10344622 7.22385
10344624 9.29789
10344633 9.23704
10344637 7.6836
10344653 3.89424
10344658 8.39676
10344674 3.08735
10344679 4.27425
10344705 5.76637
10344707 8.86037
10344713 8.51591
10344715 3.46787
10344717 3.11372
10344719 5.93287
10344721 1.81112
10344723 7.15081

Total number of rows: 28853

Table truncated, full table size 475 Kbytes.




Supplementary file Size Download File type/resource
GSM863114_1DF_CM2_MoGene-1_0-st-v1_.CEL.gz 4.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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