NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1388101 Query DataSets for GSM1388101
Status Public on Dec 31, 2014
Title 1 Hr DMSO (B7)
Sample type RNA
 
Source name HEPG2 cells no treatment (control)
Organism Homo sapiens
Characteristics cell line: HEPG2
compound: control (DMSO)
dose: 0
timepoint (hours): 1
Treatment protocol The cells (6-wells each treatment) were treated with BRD-8518 (0.005uM-3.33 uM, two-fold dilution) for 6 hr at 37C. The cells were also treated with BRD-8518 (1 uM) or Oncostatin M (100 ng/mL) for 1 hr and 24 hr at 37C. DMSO controls were set up for each timepoint. Compounds were added to the cells to a final DMSO concentration of 0.25%. Oncostatin M was dissolved in PBS and DMSO was added to the wells to bring the final concentration to 0.25%.
Growth protocol 10000 HepG2 cells are plated in each well of a Corning, black 96-well, tissue culture plate (#3904) in 40μL of DMEM/10% FBS/1x Pen-Strep-Glutamine media. The cells are then incubated overnight in a tissue culture incubator at 37°C and 5% CO2.
Extracted molecule total RNA
Extraction protocol RNA was prepared using RNeasy Minipreps (Qiagen) following the manufacture’s protocol.
Label Biotin
Label protocol Biotin labeling was performed using the Ambion WT Expression Kit (Life Technologies, Grand Island, NY) according to the manufacturer's protocol, followed by the GeneChip WT Terminal Labeling and Controls Kit (Affymetrix, Santa Clara, CA).
 
Hybridization protocol The labeled, fragmented DNA was hybridized to the Affymetrix GeneChip Human Gene ST 2.0 Array for 18 hours in a GeneChip Hybridization oven 640 at 45oC with rotation (60 rpm). The hybridized samples were washed and stained using an Affymetrix fluidics station 450.
Scan protocol After staining, microarrays were immediately scanned using an Affymetrix GeneArray Scanner 3000 7G Plus.
Description 1 Hr DMSO
Broad_B7_15
Data processing Data were normalized using the Robust Multi-Array Average method as implemented in the R package oligo.
 
Submission date May 16, 2014
Last update date Dec 31, 2014
Contact name Marek M Nageic
Organization name Broad Institute
Department Center for the Development of Therapeutics
Street address 7 Cambridge Center
City Cambridge
State/province MA
ZIP/Postal code 02142
Country USA
 
Platform ID GPL16686
Series (1)
GSE57753 Transcriptional profiling of HEPG2 cells after treatment with TRIB1-inducing compounds

Data table header descriptions
ID_REF
VALUE RMA signal intensity.

Data table
ID_REF VALUE
16650001 2.165327261
16650003 3.04395811
16650005 4.344400702
16650007 3.905021573
16650009 1.310924734
16650011 2.514511177
16650013 3.707218061
16650015 3.809736014
16650017 3.253935303
16650019 4.390885489
16650021 4.327807856
16650023 2.608783627
16650025 3.538189614
16650027 1.91772764
16650029 4.959840592
16650031 4.555764025
16650033 1.231810155
16650035 1.727570625
16650037 1.966197473
16650041 6.733029127

Total number of rows: 53617

Table truncated, full table size 1093 Kbytes.




Supplementary file Size Download File type/resource
GSM1388101_Broad_B7_15.CEL.gz 8.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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