NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1151179 Query DataSets for GSM1151179
Status Public on Nov 15, 2013
Title PBMCs from sham-operated rat, biological rep3
Sample type RNA
 
Source name peripheral blood mononuclear cells
Organism Rattus norvegicus
Characteristics tissue: peripheral blood mononuclear cells
samples collection: 2 months after sham-surgery
size of myocardial infarction: lack of an infarct area
Extracted molecule total RNA
Extraction protocol Total RNA from left ventricular (LV) tissue and peripheral blood mononuclear cells (PBMCs) samples was isolated using MagNA Pure Compact System (Roche Diagnostics GmbH, Germany) according to the manufacturer's recommendations. LVs were previously homogenized by MagNA Lyser Instrument. The amount of RNA was quantified by UV absorption (Nanodrop, LabTech International, UK) and its quality was determined using an Agilent 2100 Bioanalizer© and RNA 6000 Nano Kit (Agilent, Santa Clara, CA, USA). For all RNA samples the RNA integrity number value was above eight.
Label biotin
Label protocol Biotin-labeled ssDNA were prepared from 100 ng total RNA by using the Ambion® WT Expression Kit followed by Affymetrix® GeneChip® WT Terminal Labeling Kit according to the manufacturer's instruction.
 
Hybridization protocol Following fragmentation, 5.5 ug ssDNA were hybridized for 16 hr at 45˚C on GeneChip® Rat Gene 1.0 ST Array according to standard Affymetrix protocol. Chips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using an Affymetrix GCS 3000 GeneArray Scanner.
Description Gene expression data from peripheral blood mononuclear cells (PBMCs) of sham-operated rat
Data processing The data were analyzed with the Partek Genomics Suite software (Partek Inc, St. Louis, MO, USA) using RMA (robust multiarray average) background correction, quantile normalization, median polish method for probesets summarization, and log values of probes signals using base 2.
 
Submission date May 29, 2013
Last update date Nov 15, 2013
Contact name Dorota Anna Tulacz
E-mail(s) [email protected]
Organization name Institute of Biochemistry and Biophysics of the Polish Academy of Sciences
Department Department of Genetics
Street address Pawinskiego 5a
City Warszawa
ZIP/Postal code 02-106
Country Poland
 
Platform ID GPL6247
Series (1)
GSE47495 Transcriptional profiling of left ventricle and peripheral blood cells in rats with post-myocardial infarction

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
10700001 12.0581
10700002 6.8938
10700003 10.3283
10700004 4.94086
10700005 7.08018
10700006 2.38411
10700007 2.66876
10700008 2.11434
10700009 8.29954
10700010 3.02563
10700011 4.89718
10700012 4.22832
10700013 11.533
10700014 10.2826
10700015 8.38283
10700016 2.39809
10700017 6.23113
10700018 2.16326
10700019 2.45361
10700020 12.1309

Total number of rows: 29214

Table truncated, full table size 481 Kbytes.




Supplementary file Size Download File type/resource
GSM1151179_Sham3_PBMCs.CEL.gz 4.3 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap