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Sample GSM721675 Query DataSets for GSM721675
Status Public on May 10, 2011
Title THRA 6a mutant + T3 replicate 1
Sample type RNA
 
Source name HepG2 cells
Organism Homo sapiens
Characteristics cell line: Hep G2
genotype: RCCC-THRA mutant 6a
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 RCCC-THRA mutant 6a 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 35.6119729
7892502 20.03456185
7892503 5.074353622
7892504 574.8648418
7892505 4.829135579
7892506 13.15961642
7892507 15.60246443
7892508 8.81831348
7892509 4652.953762
7892510 15.36309963
7892511 8.822169063
7892512 92.40570382
7892513 4.615182472
7892514 1588.909271
7892515 334.118073
7892516 20.23901216
7892517 19.79630125
7892518 4.871086592
7892519 21.07053838
7892520 507.0457964

Total number of rows: 33297

Table truncated, full table size 636 Kbytes.




Supplementary file Size Download File type/resource
GSM721675.CEL.gz 3.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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