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Sample GSM721683 Query DataSets for GSM721683
Status Public on May 10, 2011
Title THRB bN mutant + T3 replicate 3
Sample type RNA
 
Source name HepG2 cells
Organism Homo sapiens
Characteristics cell line: Hep G2
genotype: HCC-THRA mutant bN
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 bN 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 32.37561339
7892502 17.56990122
7892503 4.660796013
7892504 399.3545661
7892505 5.980754044
7892506 11.04287179
7892507 18.48809103
7892508 21.97666177
7892509 4093.458462
7892510 7.464253564
7892511 5.131817891
7892512 113.4002344
7892513 7.151783818
7892514 1435.018217
7892515 382.5107756
7892516 18.37059562
7892517 27.35226574
7892518 4.565239872
7892519 48.94769075
7892520 485.9676474

Total number of rows: 33297

Table truncated, full table size 636 Kbytes.




Supplementary file Size Download File type/resource
GSM721683.CEL.gz 6.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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