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Sample GSM721677 Query DataSets for GSM721677
Status Public on May 10, 2011
Title THRA 6a mutant + T3 replicate 3
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 92.43122048
7892502 24.87879206
7892503 4.370027839
7892504 556.4342925
7892505 5.953278476
7892506 25.07484453
7892507 22.98804661
7892508 40.34289011
7892509 5094.643718
7892510 23.88036222
7892511 8.977491307
7892512 62.44812628
7892513 24.80516698
7892514 1572.345414
7892515 308.2634369
7892516 36.81097991
7892517 37.72758683
7892518 8.908203174
7892519 29.78525754
7892520 370.8308795

Total number of rows: 33297

Table truncated, full table size 636 Kbytes.




Supplementary file Size Download File type/resource
GSM721677.CEL.gz 4.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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