NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM706803 Query DataSets for GSM706803
Status Public on Apr 12, 2011
Title Sum149-control1 (Agilent-021827 miRNA v12.0)
Sample type RNA
 
Source name SUM149PT Vehicle CTRL
Organism Homo sapiens
Characteristics cell line: SUM149PT
er: ER(-)
p53: mut (M237I)
Treatment protocol SUM149PT cells were plated at 1.5 x 10^6 cells per 150 x 25mm dish with 25mL of growth media, and allowed to adhere for 48h prior to treatment. The media in each plate was replaced with 25mL fresh media containing the drug treatment.
Growth protocol SUM149PT cells were grown in Ham's F-12 media with 5% fetal bovine serume supplemented with 5 µg/mL insulin, 1 µg/mL hydrocortisone, 10 mM HEPES and Antimycotic/Antibiotic at 37°C with 5%CO2 and 85% humidity.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the miRNeasy Mini kit (Qiagen Inc., Valencia, CA, USA). RNA quality and concentration was determined by analysis with an Agilent 2100 bioanalyzer at the Center for Functional Genomics at State University of New York at Albany (Rensselaer, NY, USA)
Label cy3
Label protocol Cyanine-3 (Cy3) labeled miRNA was prepared from 100ng total RNA using the miRNA Complete Labeling and hyb kit (Agilent) according to the manufacturer's instructions
 
Hybridization protocol labeled miRNA was hybridized onto Agilent Human miRNA microarrays v3 (G4771-A) rel 12.0 according to the manufacturer's instructions.
Scan protocol The arrays were scanned on a Agilent G2565C scanner using the standard settings for 8x15k array slides.
Description miRNA expression after treatment with vehicle (ethanol and DMSO) for 48h
Data processing The scanned images were analyzed with Feature Extraction Software 10.1.1 (Agilent) using default parameters (protocol miRNA-v1_10_Apr08 and Grid: 021827_D_20081121) to obtain background subtracted and spatially detrended Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded.
 
Submission date Apr 12, 2011
Last update date Apr 12, 2011
Contact name Sridar V Chittur
E-mail(s) [email protected]
Phone 518-591-7215
Organization name SUNY-University at Albany
Department Center for Functional Genomics
Lab Microarray Core
Street address One Discovery Drive, CRC 342G
City Rensselaer
State/province NY
ZIP/Postal code 12144
Country USA
 
Platform ID GPL10850
Series (2)
GSE28543 Expression Profiling of Inflammatory Breast Cancer Cells Treated with the Novel Histone Deacetylase Inhibitor, CG-1521 (Agilent miRNA v12.0)
GSE28544 Expression Profiling of Inflammatory Breast Cancer Cells Treated with the Novel Histone Deacetylase Inhibitor, CG-1521

Data table header descriptions
ID_REF
VALUE GeneSpring GX10 normalized intensity (gTotalGeneSignal(normalized))

Data table
ID_REF VALUE
miRNABrightCorner30 4.090971
DarkCorner 1.2011615
hsa-miR-720 11.017587
hsa-miR-587 -0.4822339
hsa-miR-1236 -0.4822339
hsa-miR-607 -0.4822339
hsa-miR-1253 -0.2934279
hsa-miR-369-3p -0.004732668
hsa-miR-657 -0.4822339
hsa-miR-526b -0.006588668
hsa-miR-515-3p -0.002051562
hsa-miR-586 -0.4822339
hsa-miR-485-5p -0.29302287
hsa-miR-507 -0.006816983
hsa-miR-551b* -0.4822339
hsa-miR-326 -0.29025435
hsa-miR-146b-3p -0.4822339
hsa-miR-1283 -0.2937317
hsa-miR-622 -0.27998543
hsa-miR-556-5p -0.4822339

Total number of rows: 961

Table truncated, full table size 23 Kbytes.




Supplementary file Size Download File type/resource
GSM706803_US83803556_252182712213_S01_miRNA-v1_10_Apr08_1_1.txt.gz 902.0 Kb (ftp)(http) TXT
Processed data included within Sample table

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