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Sample GSM289655 Query DataSets for GSM289655
Status Public on May 20, 2008
Title New 3 hr 2
Sample type RNA
 
Source name MCF-7 cells treated with E2 for 3h.
Organism Homo sapiens
Characteristics breast adenocarcinoma from 69yr old female caucasian
Treatment protocol After MCF-7 cells were grown to 75% to 80% confluence in MEM supplemented with 10% FBS, the cells were serum starved in DMEM/F-12 without phenol red (Invitrogen) and FBS for 24 h. MCF-7 cells were then treated with vehicle or E2 at a concentration of 10–9 mol/L for 3 and 6 h. All experiments were performed in triplicate.
Growth protocol MCF-7 cells (American Type Culture Collection) were maintained in MEM (Invitrogen) containing 25 units/mL penicillin, 25 units/mL streptomycin, and 10% fetal bovine serum (FBS) at 37°C and 5% CO2.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from the MCF-7 breast cancer cell line using Tri-Reagent (Sigma) according to the manufacturer's instruction. Total RNA samples were treated with DNase I (Ambion) for 20 min at 37°C according to the product manual.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
 
Hybridization protocol Following fragmentation, cRNA were hybridized to Human Genome U133Plus2.0 GeneChips. GeneChips were washed and stained in an Affymetrix Fluidics Station.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Description biological replicate: New 3 hr 1,New 3 hr 2,New 3 hr 3
Data processing Probe level data was converted to probe set expression values using RMA (Irizarry RA et al., Biostatistics 2003 Apr;4(2):249-64).
 
Submission date May 20, 2008
Last update date Aug 28, 2018
Contact name Zhihong Lin
E-mail(s) [email protected]
Organization name Northwestern University
Department Obstetrics and Gynecology
Street address 303 East Superior Street
City Chicago
State/province IL
ZIP/Postal code 60611
Country USA
 
Platform ID GPL570
Series (1)
GSE11506 Novel Estrogen Receptor-{alpha} Binding Sites and Estradiol Target Genes Identified by ChIP Cloning in Breast Cancer.
Relations
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
1007_s_at 12.59292533
1053_at 9.774089877
117_at 7.107427829
121_at 10.31311113
1255_g_at 4.962507497
1294_at 7.319082457
1316_at 6.950459698
1320_at 6.62039225
1405_i_at 5.422954535
1431_at 5.053615441
1438_at 8.284905681
1487_at 8.860338584
1494_f_at 7.813441007
1552256_a_at 10.11500635
1552257_a_at 9.194258468
1552258_at 6.640899646
1552261_at 6.515617314
1552263_at 6.474169295
1552264_a_at 8.951666691
1552266_at 6.629375395

Total number of rows: 54675

Table truncated, full table size 1212 Kbytes.




Supplementary file Size Download File type/resource
GSM289655.CEL.gz 5.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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