NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM606067 Query DataSets for GSM606067
Status Public on Mar 31, 2011
Title Control, doxcycline 24 h, rep 1
Sample type RNA
 
Source name TW01Tet
Organism Homo sapiens
Characteristics tissue: nasopharyngeal carcinoma
cell line: TW01Tet
immortalization method: EBV negative
Treatment protocol Cells were treated with doxycycline (50 nanogram/ml) for 24 h.
Growth protocol Cells were grown to log-phase in DMEM supplemented with 10% tetracycline-free fetal bovine serum before induction.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using a RNeasy Mini kit (Qiagene), according to the manufacturer’s instructions. A 2-round amplification was performed with the ExpressArt TRinucleotide mRNA Amplification Kit (AmpTec) according to the manufacturer’s instructions.
Label biotin
Label protocol Single-stranded cDNA was generated from the amplified cRNA with the WT cDNA Synthesis Kit (Affymetrix) and then fragmented and labeled with the WT Terminal Labeling Kit (Affymetrix).
 
Hybridization protocol Samples were hybridized with GeneChip Human Gene 1.0 ST Arrays (Affymetrix) and scanned at the NHRI Microarray Core Facility (Miaoli County, Taiwan).
Scan protocol Array scanning was performed according to the manufacturer's instruction (Affymetrix).
Description Cell densitiy was maintained at 150,000 / ml before induction.
Data processing The data were analyzed using Affymetrix Expression Console™ Software (version 1.1) default analysis settings and RMA (Robust Multi-Array) summarization and normalization options.
 
Submission date Oct 07, 2010
Last update date Mar 31, 2011
Contact name Su-Fang Lin
E-mail(s) sflin1@gmail.com
Organization name National Health Research Institutes, Taiwan
Department NICR
Lab R2-1211
Street address No 35, Keyan Road, Zhunan Town
City Miaoli Conunty
ZIP/Postal code 35053
Country Taiwan
 
Platform ID GPL6244
Series (2)
GSE24586 Expression profiling of host genes modulated by Epstein-Barr virus Rta in nasopharyngeal carcinoma cells
GSE24587 Epstein–Barr virus (EBV) Rta-mediated cell cycle arrest enables permissive replication of EBV and Kaposi’s sarcoma-associated herpesvirus in 293 cells

Data table header descriptions
ID_REF
VALUE RMA signal intensity (log2 based values)

Data table
ID_REF VALUE
7896736 5.478847
7896738 2.49704
7896740 2.704047
7896742 7.123342
7896744 3.864399
7896746 7.603771
7896748 7.931089
7896750 2.667372
7896752 7.732386
7896754 5.188334
7896756 4.401522
7896759 5.303232
7896761 7.030614
7896779 6.479792
7896798 6.880328
7896817 8.363596
7896822 9.23945
7896859 5.00772
7896861 3.164277
7896863 5.183508

Total number of rows: 33297

Table truncated, full table size 549 Kbytes.




Supplementary file Size Download File type/resource
GSM606067.CEL.gz 4.2 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