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Sample GSM214810 Query DataSets for GSM214810
Status Public on Aug 23, 2007
Title HMVEC_vehicle_rep1
Sample type RNA
 
Source name Human Microvascular Endothelial Cells, vehicle treated 24 h
Organism Homo sapiens
Characteristics Primary culture of human lung microvascular endothelial cells (CC-2527)
Biomaterial provider Cambrex
Treatment protocol HMVEC at passage 7 were plated in 6 cm culture dishes with 3 ml culture medium, at a density of 1,000,000 cells/dish. After 2 days (confluence 90%) the cells were incubated for 24 hours in 3 ml culture media containing vehicle (10 μl sterile PBS).
Growth protocol Human microvascular EC (HMVEC; CC-2527, Cambrex) were cultured in EGM-2 MV BulletKit medium, containing endothelial cell basal medium-2, human epidermal growth factor (hEGF), hydrocortisone, human basal fibroblast growth factor (hFGF-B), vascular endothelial growth factor, recombinant insulin-like growth factor 1, ascorbic acid, gentamicin, amphotericin-B, and 5% fetal bovine serum (FBS) and maintained at 37 ºC in a humidified atmosphere of 5% CO2 and 95% air.
Extracted molecule total RNA
Extraction protocol 24 hours after treatment with the vehicle cells were harvested and total RNA was isolated using Ultraspec RNA isolation reagent (Biotecx Laboratories), according to the manufacturer’s instructions.
Label biotin
Label protocol Two hundred ng of total RNA was reverse transcribed and amplified overnight with T7 RNA polymerase and labeled with biotin following the manufacturer’s protocol.
 
Hybridization protocol 1.5 microgram of biotin-labeled aRNA was hybridized to Illumina Human Ref-6 v1 BeadChips at 58 °C overnight. BeadChips were incubated with Cy3 streptavidin and washed according to the manufacturer’s protocol.
Scan protocol The hybridized BeadChips were scanned by Illumina BeadScan confocal scanner and analyzed by Illumina's BeadStudio version 1.5.1.3. aRNA synthesis, hybridization and scanning were performed by the Microarray Core Laboratory of the University of Texas Health Science Center.
Description This sample is the first of 3 replicates.
Data processing Initial analysis was done using Illumina’s Beadstudio version 1.5.1.3. This array was used as "reference array" for normalization by rank-invariant method.
 
Submission date Aug 02, 2007
Last update date Aug 14, 2011
Contact name Marjan Boerma
E-mail(s) mboerma@uams.edu
Phone 501-686-6882
Organization name University of Arkansas for Medical Sciences
Street address 4301 West Markham, Slot 725
City Little Rock
State/province AR
ZIP/Postal code 72205
Country USA
 
Platform ID GPL2507
Series (1)
GSE8686 Gene expression profiling in three primary human cell lines treated with atorvastatin or an inhibitor of Rho kinase

Data table header descriptions
ID_REF
RAW background subtracted
VALUE rank-invariant normalized
DETECTION P-VALUE detection p-value

Data table
ID_REF RAW VALUE DETECTION P-VALUE
GI_10047089-S -9.5 -9.5 0.22808174
GI_10047091-S 19.3 19.3 0.94199077
GI_10047093-S 331.3 331.3 1
GI_10047099-S 1885.5 1885.5 1
GI_10047103-S 866 866 1
GI_10047105-S 848.2 848.2 1
GI_10047121-S -8 -8 0.26763349
GI_10047123-S 188.1 188.1 1
GI_10047133-A -14.3 -14.3 0.11931444
GI_10047133-I -4.1 -4.1 0.38562953
GI_10092578-S -7.7 -7.7 0.27620303
GI_10092585-S 59.9 59.9 1
GI_10092596-S 87.5 87.5 1
GI_10092600-S 459.3 459.3 1
GI_10092602-S -0.1 -0.1 0.50164799
GI_10092603-S 3.7 3.7 0.61964403
GI_10092611-A 706 706 1
GI_10092616-S 22.4 22.4 0.96506262
GI_10092618-S 2238.2 2238.2 1
GI_10092638-S 1109.7 1109.7 1

Total number of rows: 47293

Table truncated, full table size 1472 Kbytes.




Supplementary file Size Download File type/resource
GSM214810.txt.gz 2.5 Mb (ftp)(http) TXT
GSM214810_1.txt.gz 2.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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