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Sample GSM721671 Query DataSets for GSM721671
Status Public on May 10, 2011
Title THRA aI mutant + T3 replicate 3
Sample type RNA
 
Source name HepG2 cells
Organism Homo sapiens
Characteristics cell line: Hep G2
genotype: HCC-THRA mutant al
treatment: with 100 nM T3 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 al treated with 100 nM T3 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 25.64265021
7892502 22.78928011
7892503 4.518911334
7892504 530.7335753
7892505 4.307284554
7892506 10.24774049
7892507 33.90569774
7892508 29.44133326
7892509 3869.261502
7892510 5.599859269
7892511 4.334759288
7892512 89.21763707
7892513 4.850180192
7892514 1459.789911
7892515 395.1257592
7892516 29.67668952
7892517 35.89353572
7892518 6.865990592
7892519 24.04478834
7892520 490.0757038

Total number of rows: 33297

Table truncated, full table size 636 Kbytes.




Supplementary file Size Download File type/resource
GSM721671.CEL.gz 6.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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