NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM523724 Query DataSets for GSM523724
Status Public on Mar 21, 2012
Title Kasumi-1 300nM TSA 9 hours [mRNA profiling]
Sample type RNA
 
Channel 1
Source name Mock Treated Kasumi-1
Organism Homo sapiens
Characteristics agent: 1x PBS
cell line: Kasumi-1 human leukemia cell line
Biomaterial provider ATCC
Treatment protocol 1x PBS for 9 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 300nM TSA, 9 hours, Treated Kasumi-1
Organism Homo sapiens
Characteristics agent: 300nM TSA
cell line: Kasumi-1 human leukemia cell line
time point: 9 hours
Biomaterial provider ATCC
Treatment protocol 300nM TSA for 9 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 Effect of 300nM TSA at 9 hours on gene expression in Kasumi-1 cells
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 Mar 18, 2010
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 GPL4133
Series (1)
GSE20945 Effects of DAC treatment

Data table header descriptions
ID_REF
VALUE Normalized log ratio data: log2(CH2/CH1)
CH1_SIG_MEDIAN Median spot value of channel 1
CH1_BKD_MEDIAN Background median spot value of channel 1
CH2_SIG_MEDIAN Median spot value of channel 2
CH2_BKD_MEDIAN Background median spot value of channel 2

Data table
ID_REF VALUE CH1_SIG_MEDIAN CH1_BKD_MEDIAN CH2_SIG_MEDIAN CH2_BKD_MEDIAN
1 0.135156600885598 32062 47 80825.2 58
2 0.130231793018934 47 48 61 58
3 -0.0405980225624834 52 48 62 58
4 -0.0916591776459328 52 49 59 58
5 -0.0926895228596644 53 49 61 59
6 -0.0594762469799801 53 49 63 58
7 0.0378066990316454 52 49 67 59
8 -0.0310030512375134 51.5 50 61.5 58
9 -0.0513376886837961 53 49 63.5 56
10 -0.0159867566333232 52 50 63.5 58
11 -0.0573385908091916 52 49 61 59
12 -0.102040215587399 178 49 344 57
13 -0.527423145778616 92.5 50 113 57
14 0.784585497083102 345 49 1270 58
15 0.63260662742698 112 50 353.5 58
16 -0.531525795120976 5985.5 49 8658.5 59
17 0.0693237471666126 59 49 90.5 60
18 -0.663491015618798 204 50 266 58
19 0.555676542013353 34267.9 49 116936 59
20 0.0512069938095063 60 49 92 59

Total number of rows: 45220

Table truncated, full table size 1756 Kbytes.




Supplementary file Size Download File type/resource
GSM523724.txt.gz 14.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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