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Sample GSM277401 Query DataSets for GSM277401
Status Public on Aug 23, 2008
Title Endothelial cells from right coronary artery, rep 3
Sample type RNA
 
Channel 1
Source name right coronary endothelial cells
Organism Sus scrofa
Characteristics Animal 3
Growth protocol Reference endothelial cells were grown in M199 supplemented with antibiotic/mycotic, FBS, and porcine serum. Passage 3 cells were used.
Extracted molecule total RNA
Extraction protocol Qiagen RNeasy Micro kit following manufacturer's protocol
Label Cy5
Label protocol Messenger RNA was amplified using a MessageAmp II aRNA amplification kit (Ambion). two rounds of amplification were performed, and aminoallyl-UTP was used in the final round to provide reactive groups for dye incorporation. The RNA samples were labeled with Cy5 dyes, and reference RNA sample was labeled with Cy3 dyes.
 
Channel 2
Source name reference RNA
Organism Sus scrofa
Characteristics cultured porcine aortic endothelial cells (passage 3)
Growth protocol Reference endothelial cells were grown in M199 supplemented with antibiotic/mycotic, FBS, and porcine serum. Passage 3 cells were used.
Extracted molecule total RNA
Extraction protocol Qiagen RNeasy Micro kit following manufacturer's protocol
Label Cy3
Label protocol Messenger RNA was amplified using a MessageAmp II aRNA amplification kit (Ambion). two rounds of amplification were performed, and aminoallyl-UTP was used in the final round to provide reactive groups for dye incorporation. The RNA samples were labeled with Cy5 dyes, and reference RNA sample was labeled with Cy3 dyes.
 
 
Hybridization protocol • Make hybridization buffer fresh each time. • Add 38 ul hybridization buffer to 12 ul fragmented Cy Dye labeled aa-aRNA. • Add 1ul each poly dA and appropriate Cot-1 DNA. • Heat at 95ºC for 2 minutes and put on ice to cool down. • Mix well and load sample to the array slide with lifter cover slip. • Hybridize overnight in 42ºC water bath.
Scan protocol Scanned by GenePix 4000B and quantified using GenePix software
Description Endothelial cells were freshly harvest from right coronary, left and right iliac arteries from four pigs.
Data processing LOWESS normalized, inlcude genes with signal in at least 8 of the 12 arrays, Agilent GeneSpring GX was used.
 
Submission date Mar 25, 2008
Last update date Aug 23, 2008
Contact name Ji Zhang
E-mail(s) ji.z@duke.edu
Phone 919-660-5125
Fax 919-684-4488
Organization name Duke University
Department Department of Biomedical Engineering
Lab Cardiovascular simulations
Street address Room 136 Hudson Hall
City Durham
State/province NC
ZIP/Postal code 27708
Country USA
 
Platform ID GPL3461
Series (1)
GSE10938 In vivo endothelial transcriptional profiles of porcine coronary and iliac arteries

Data table header descriptions
ID_REF
VALUE Lowess normalized log2 ratio (Cy5/Cy3) representing test/reference

Data table
ID_REF VALUE
SS00000001
SS00000002
SS00000003
SS00000004
SS00000005 0.270229907
SS00000006
SS00000007
SS00000008 -3.361416385
SS00000009 2.183962835
SS00000010 0.955312803
SS00000011 -0.100051014
SS00000012 1.24610401
SS00000013
SS00000014 0.168642036
SS00000015
SS00000016
SS00000017
SS00000018 -1.411195433
SS00000019 -2.058893689
SS00000020 0.619178216

Total number of rows: 10677

Table truncated, full table size 191 Kbytes.




Supplementary file Size Download File type/resource
GSM277401.gpr.gz 1.1 Mb (ftp)(http) GPR
Processed data included within Sample table

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