NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM721678 Query DataSets for GSM721678
Status Public on May 10, 2011
Title THRB bN mutant + vehicle replicate 1
Sample type RNA
 
Source name HepG2 cells
Organism Homo sapiens
Characteristics cell line: Hep G2
genotype: HCC-THRA mutant bN
treatment: with vehicle for 6h
Treatment protocol The HepG2 transformant pools expressing ectopic wildtype THRA, THRB, an HCC-TR mutant (αΙ or βN), a RCCC-TR mutant (6α or 15β), or the empty plasmid control were treated with 100 nM T3 or with ethanol carrier alone for 6h in DMEM containing 10% hormone-stripped fetal bovine serum.
Growth protocol HepG2 cells were maintained at 37°C in Dulbecco's Modified Eagle's Medium (DME) supplemented with 10% fetal bovine serum using bicarbonate buffer and a 5% CO2 atmosphere.
Extracted molecule total RNA
Extraction protocol The cells were harvested and the RNA was isolated using an RNeasy kit (Qiagen, Valencia CA).
Label biotin
Label protocol The purified RNA was provided to the University of California, Davis, Cancer Center Gene Expression Resource for subsequent cDNA probe generation and hybridization to Affymetrix GeneChip Human Gene 1.0 ST microarrays (Affymetrix Incorporated, Santa Clara CA).
 
Hybridization protocol The purified RNA was provided to the University of California, Davis, Cancer Center Gene Expression Resource for subsequent cDNA probe generation and hybridization to Affymetrix GeneChip Human Gene 1.0 ST microarrays (Affymetrix Incorporated, Santa Clara CA).
Scan protocol The purified RNA was provided to the University of California, Davis, Cancer Center Gene Expression Resource for subsequent cDNA probe generation and hybridization to Affymetrix GeneChip Human Gene 1.0 ST microarrays (Affymetrix Incorporated, Santa Clara CA).
Description HepG2 cells stably expressing HCC-THRA mutant bN treated with vehicle for 6h.
Data processing The raw microarray data was normalized by the Robust Multichip Array (RMA) method using R software.
 
Submission date May 09, 2011
Last update date Sep 01, 2016
Contact name Scott Andrew Ochsner
E-mail(s) [email protected]
Phone 713-798-6227
Organization name Baylor College of Medicine
Department Molecular and Cellular Biology
Lab SPP: Signaling Pathways Project
Street address One Baylor Plaza
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platform ID GPL6244
Series (1)
GSE29159 Mutant thyroid hormone receptors (TRs) isolated from distinct cancer types display distinct target gene specificities: a unique regulatory repertoire associated with renal clear cell carcinomas.
Relations
Reanalyzed by GSE86357

Data table header descriptions
ID_REF
VALUE unlogged RMA normalized signal intensity

Data table
ID_REF VALUE
7892501 29.96409182
7892502 15.0515681
7892503 5.216797854
7892504 399.5281709
7892505 7.916092577
7892506 18.70262944
7892507 8.554245545
7892508 8.005811446
7892509 3929.33892
7892510 9.739173948
7892511 4.880849941
7892512 76.80021779
7892513 5.951559369
7892514 1550.601172
7892515 368.9284867
7892516 21.74224742
7892517 13.41199247
7892518 4.484722625
7892519 32.16541503
7892520 450.1014945

Total number of rows: 33297

Table truncated, full table size 636 Kbytes.




Supplementary file Size Download File type/resource
GSM721678.CEL.gz 6.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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