NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM335384 Query DataSets for GSM335384
Status Public on Dec 01, 2008
Title 3H LPS, patient 88, responder
Sample type RNA
 
Source name arterial blood mononuclear cells activated by LPS, responder
Organism Homo sapiens
Characteristics race: Caucasian
tissue: blood
cell type: mononuclear cells
treatment: LPS
disease: chronic coronary occlusion
collateral flow response: sufficient
Treatment protocol Subsequently, monocytes were negatively isolated using immunomagnetic beads for stimulation with 10ng/ml LPS for 3h.
Extracted molecule total RNA
Extraction protocol mRNA was extracted from 10 and 10 patients from the extreme ends of the spectrum (very high vs. very low CFI), by using Trizol (Invitrogen) with an RNEasy Micro column cleanup (Qiagen), who were matched for age, sex, medication and other factors that influence collateral artery growth.
Label Biotin
Label protocol Default in vitro transcription to produced Biotinylated antisense aRNA by using the Illumina Totalprep RNA amplification kit (#IL1791, Ambion).
 
Hybridization protocol 750ng of biotinylated cRNA was hybridized onto the HumanRef-8 Expression BeadChips according to the manufacturer's specifications.
Scan protocol According to the manufacturer, performed by ServiceXS (http://www.servicexs.com).
Description patient: Caucasian patients were included who underwent percutaneous coronary intervention (PCI) of a total coronary occlusion. Exclusion criteria were previous myocardial infarction, cardiac surgery, depressed left ventricular function, diabetes mellitus, neoplastic or inflammatory disease. Invasive coronary collateral flow index (CFI) measurements were then performed. Patients were dichotomized as either sufficient (CFI>0.37) or insufficient (CFI≤0.37) collateral responders (0.37 was the median CFI of this patient group).
tissue: mononuclear cells were collected from 50 ml of arterial blood using Ficoll separation
Data processing Gene expression analysis was performed by using Illumina's Beadstudio v3 software, followed by a quantile inter-array normalization (R, Bioconductor).
 
Submission date Oct 21, 2008
Last update date Jul 28, 2010
Contact name Oscar Leonard Volger
E-mail(s) [email protected], [email protected]
Organization name Academic Medical Center
Department Cardiology
Street address Meibergdreef 15
City Amsterdam
State/province Noor Holland
ZIP/Postal code 1105 AZ
Country Netherlands
 
Platform ID GPL5104
Series (1)
GSE13290 Circulating Cells in Coronary Collateral Artery Growth II

Data table header descriptions
ID_REF
VALUE avg Signal

Data table
ID_REF VALUE
ILMN_10001 10.66836236
ILMN_10011 8.141351339
ILMN_10016 6.675316909
ILMN_10021 6.969156183
ILMN_10025 9.741830002
ILMN_1003 8.346113593
ILMN_10033 7.2826205
ILMN_10035 6.56547749
ILMN_1004 6.635090835
ILMN_10054 7.262311986
ILMN_10057 9.408517931
ILMN_10062 7.422753354
ILMN_10063 7.142795211
ILMN_10073 8.613874322
ILMN_10076 6.842390784
ILMN_10077 7.896151476
ILMN_10078 6.731499651
ILMN_10080 6.400787596
ILMN_10085 8.256915458
ILMN_10087 7.363836274

Total number of rows: 7816

Table truncated, full table size 172 Kbytes.




Supplementary file Size Download File type/resource
GSM335384_10035235.txt.gz 311.0 Kb (ftp)(http) TXT
Processed data included within Sample table

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