NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM843857 Query DataSets for GSM843857
Status Public on Mar 21, 2012
Title DAC Treated 104 Day 14 [mRNA profiling]
Sample type RNA
 
Channel 1
Source name Mock treated primary leukemia 104 at day 14
Organism Homo sapiens
Characteristics treatment: 1XPBS for 72 hours
cell type: Breast Cancer
Treatment protocol 10nM DAC for 72 hours
Growth protocol McCoy's 5A medium with 10% BCS and 1x PBS
Extracted molecule total RNA
Extraction protocol TriZol extraction followed by RNeasy kit (Qiagen) clean-up with on-column DNase treatment
Label Cy3
Label protocol Agilent low RNA input linear amplification kit
 
Channel 2
Source name DAC treated primary leukemia 104 at day 14
Organism Homo sapiens
Characteristics treatment: 10nM DAC
cell type: Breast Cancer
time: day 14
Treatment protocol 10nM DAC for 72 hours
Growth protocol McCoy's 5A medium with 10% BCS and 1x PBS
Extracted molecule total RNA
Extraction protocol TriZol extraction followed by RNeasy kit (Qiagen) clean-up with on-column DNase treatment
Label Cy5
Label protocol Agilent low RNA input linear amplification kit
 
 
Hybridization protocol Samples were amplified and labeled using Quick Amp Labeling Kit (Cat# 5190-0447, Agilent Technologies), Full Spectrum Primers (Cat# RA300A-2, System Bioscience), Cynine-3-CTP and Cynine-5-CTP (Perkin Elmer), and hybridized using Gene Expression Hybridization Kit by following manufacturer's protocol (G4140-90050, Agilent Technologies)
Scan protocol Microarrays were scanned with Agilent G2565BA microarray scanner under default settings recommended by Agilent Technologies for gene expression microarrays with 100% PMT and 5 micrometer resolutions. Data were extracted using Feature Extraction Software v9.5.3.1 (Agilent Technologies) and protocol for gene expression microarrays.
Description Characterization of gene expression changes after treatment with the DNA methylation inhibitor DAC
Data processing Log ratio of red signal to green signal was calculated after loess normalization as implemented in the Limma package from Bioconductor
 
Submission date Dec 06, 2011
Last update date Mar 21, 2012
Contact name Leander Van Neste
Organization name Ghent University
Department Molecular Biotechnology
Lab Bioinformatics and Computational Genomics
Street address Coupure Links 653
City Ghent
ZIP/Postal code 9000
Country Belgium
 
Platform ID GPL6480
Series (1)
GSE20945 Effects of DAC treatment

Data table header descriptions
ID_REF
VALUE loess normalized log2 ratio of DAC treatment over mock treatment

Data table
ID_REF VALUE
A_23_P100001 0.022082391
A_23_P100011 -0.226855665
A_23_P100022 0.271227155
A_23_P100056 0.100956386
A_23_P100074 -0.102587681
A_23_P100092 0.046001127
A_23_P100103 0.222626153
A_23_P100111 0.289184781
A_23_P100127 -0.309241111
A_23_P100133 0.026205117
A_23_P100141 0.035396762
A_23_P100156 0.268399021
A_23_P100177 -0.04143346
A_23_P100189 0.132655802
A_23_P100196 -0.313083429
A_23_P100203 -0.027719095
A_23_P100220 0.259296709
A_23_P100240 -0.103935113
A_23_P10025 -0.197318616
A_23_P100263 0.581315828

Total number of rows: 41000

Table truncated, full table size 1003 Kbytes.




Supplementary file Size Download File type/resource
GSM843857_jhu_251485068035_S01_GE2_107_Sep09_1_4_104_Mock_D14-Cy3_104_AZA_D14-Cy5.txt.gz 15.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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