NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1242414 Query DataSets for GSM1242414
Status Public on Oct 07, 2014
Title A612_02_R40_DMSO_GF
Sample type RNA
 
Source name brain tumor initiating cells (BTIC)
Organism Homo sapiens
Characteristics cell type: brain tumor initiating cells (BTIC)
treatment: DMSO
gf: yes
btic culture: BTIC_3
Treatment protocol Cells were cultured in growth factor free medium for 16 hours prior to treatment. After starvation, cells were treated with 1 µM Sunitinib in the treatment groups or 0.00025 % DMSO in the control groups either with or without supplementation of recombinant growth factors PDGF-A/B and VEGFA (25 ng/ml) for 6 hours before harvest.
Growth protocol BTICs were cultured in stem-cell permissive RHB-A media (Stem Cell, Cambridge, UK) supplemented with 20 ng/ml of each human recombinant epidermal growth factor (EGF; R&D Systems, Minneapolis, USA) and human recombinant basic fibroblast growth factor (FGF; Peprotech, Hamburg, Germany).
Extracted molecule total RNA
Extraction protocol Cells were washed twice with ice-cold PBS and harvested in RLT-lysis buffer (provided in the RNeasy Kit, Qiagen, Hilden, Germany) for subsequent RNA-extraction
Label biotin
Label protocol cRNA and ssDNA were prepared from 0.3 µg totalRNA according to the Ambion WT Expression Kit manual. Fragmentation and terminal biotinylation were performed using the Affymetrix Terminal Labeling Kit.
 
Hybridization protocol 3 μg of labelled products were hybridized, washed and stained in an Affymetrix GeneTitan system.
Scan protocol Arrays were scanned in an Affymetrix GeneTitan system.
Data processing Raw intensities were quantile normalized and summarized with the RMA (Robust Multichip Average) expression measure described in Irizarry et al, Biostatistics (2003)
For the final analysis, only those features were used that could be mapped to EntrezIDs.
 
Submission date Sep 30, 2013
Last update date Oct 08, 2014
Contact name Christian W Kohler
E-mail(s) [email protected]
Organization name University of Regensburg
Department Institute of Functional Genomics
Lab Statistical Bioinformatics
Street address Am BioPark 9
City Regensburg
State/province Bavaria
ZIP/Postal code 93053
Country Germany
 
Platform ID GPL11532
Series (1)
GSE51305 Gene expression profiles of Sunitinib-treated but not untreated short-term serum-free cultures predict treatment response of human high-grade gliomas in vitro

Data table header descriptions
ID_REF
VALUE RMA processed data is on log2 scale

Data table
ID_REF VALUE
7892501 4.44753936755688
7892502 4.00737334663573
7892503 2.30800187305372
7892504 5.66802249943912
7892505 2.44795024923306
7892506 2.46277548746568
7892507 3.37188904332954
7892508 4.77363137799122
7892509 10.5372895712685
7892510 4.48412101674264
7892511 3.52431514258208
7892512 4.28120052024688
7892513 3.3944873964546
7892514 10.2811784613023
7892515 7.54593573831609
7892516 2.49940872766506
7892517 5.73181492533259
7892518 2.45449214652018
7892519 3.13896736145402
7892520 7.14642146053205

Total number of rows: 33297

Table truncated, full table size 809 Kbytes.




Supplementary file Size Download File type/resource
GSM1242414_A612_02_R40_DMSO_GF.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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