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Sample GSM592131 Query DataSets for GSM592131
Status Public on Jun 01, 2011
Title total RNA, MCF7 5-Fluoro-Uracil (5FU) plus 17-β estradiol (pharmacological dose) treated, 10h, biological replicate #3
Sample type RNA
 
Source name MCF7 cells, 5-Fluoro-Uracil (5FU) plus 17-β estradiol (E2) pharmacological dose treated, 10 hours, total RNA, biological replicate #3
Organism Homo sapiens
Characteristics cell line: MCF7 cells
agent: 5-Fluoro-Uracil (5FU) plus 17-β estradiol (E2) pharmacological dose
time point: 10 hours
population: total RNA
biological replicate: #3
Biomaterial provider ICLC
Treatment protocol MCF7 cells were seeded on 10cm Petri dishes and grown in estrogen-depleted conditions, D-MEM w/o Phenol Red, 10% Dextrane-Charcoal treated serum, 2mM glutamine, 1X penicillin/streptomycin. After 24h cells were treated at the same time with 5FU and E2 for 10 hours at a final concentration respectively of 375 μM and 100 nM.
Growth protocol MCF7 cells were cultured in Dulbecco Modified Eagle Medium (D-MEM) without Phenol Red supplemented with 10% Dextrane-Charcoal treated fetal bovine serum (FBS), 2mM glutamine, 100 units/ml penicillin, and 100 mg/ml streptomycin at 37 °C in a humidified atmosphere of 5% CO2.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the Agilent Total RNA Isolation Mini kit according to the manufacturer’s protocol. RNA was quantified using a spectrophotometer and its quality was checked by agarose gel electrophoresis as well as by Agilent 2100 Bioanalyzer platform, following the manifacturer’s guidelines for sample preparation and analysis of data (Agilent 2100 Bioanalyzer 2100 Expert User's Guide, http://www.agilent.com).
Label Cy3-CTP
Label protocol G4140-90040_One-Color_GE_5.7 (https://www.chem.agilent.com/Library/usermanuals/Public/G4140-90040_GeneExpression_One-Color_v6.0.pdf)
 
Hybridization protocol Hybridization, blocking and washing were performed according to Agilent protocol: “One-Color Microarray-Based Gene Expression Analysis (Quick Amp Labeling)”: (https://www.chem.agilent.com/Library/usermanuals/Public/G4140-90040_GeneExpression_One-Color_v6.0.pdf).
Scan protocol Hybridized microarray slides were scanned with an Agilent DNA Microarray Scanner (G2505C, Agilent Technologies, Santa Clara, CA) at 5 micron resolution with the manufacturer’s software (Agilent ScanControl 8.1.3). The scanned TIFF images were analyzed numerically using the Agilent Feature Extraction Software version 10.7.7.1 according to the Agilent standard protocol GE1_107_Sep09.
Description Total RNA sample extracted from 5-Fluoro-Uracil (5FU) plus 17-β estradiol (E2) pharmacological dose treated MCF7 cells grown in estrogen-depleted conditions.
Data processing Agilent Feature Extraction Software version 10.7.7.1 (standard protocol GE1_107_Sep09) was used for data extraction, background correction and flagging of non-uniform features. The output of Feature Extraction was analyzed with the R software environment for statistical computing (http://www.r-project.org/) and the Bioconductor library of biostatistical packages (http://www.bioconductor.org/). Signal intensities across arrays were normalized with the quantile normalization algorithm.
 
Submission date Sep 09, 2010
Last update date Jun 01, 2011
Contact name Toma Tebaldi
E-mail(s) tebaldi@science.unitn.it
URL http://portale.unitn.it/cibio/portalpage.do?channelId=-54340&channel2Id=-54565&content_OID=269530&page=/jsp/editorial/editorial.jsp&programId=269532
Organization name Centre for Integrative Biology
Lab Transcriptional Network Lab
Street address via delle Regole 101
City Mattarello - Trento
State/province Trento
ZIP/Postal code 38123
Country Italy
 
Platform ID GPL6480
Series (1)
GSE24065 Crossroads of the p53, ER, NFkB stress response networks

Data table header descriptions
ID_REF
SIGNAL_RAW Raw intensity signal assigned by the Agilent Feature Extraction Software version 10.7.7.1.
FLAG Detection call assigned by the Agilent Feature Extraction Software version 10.7.7.1.
VALUE Quantile normalized log2 transformed intensity signal.

Data table
ID_REF SIGNAL_RAW FLAG VALUE
A_23_P100001 8360.708 P 13.308
A_23_P100011 325.2387 P 8.8213
A_23_P100022 38.0205 A 5.5844
A_23_P100056 18.6624 A 3.0048
A_23_P100074 4560.773 P 12.4736
A_23_P100092 1186.5936 P 10.6286
A_23_P100103 106.9796 P 7.1413
A_23_P100111 91.7492 P 6.9147
A_23_P100127 132.0543 P 7.4655
A_23_P100133 32.678 A 5.3736
A_23_P100141 463.6734 P 9.3217
A_23_P100156 917.7753 P 10.2668
A_23_P100177 18.8854 A 3.0427
A_23_P100189 37.3612 A 5.5588
A_23_P100196 1935.9988 P 11.2819
A_23_P100203 4413.8633 P 12.4313
A_23_P100220 8922.149 P 13.3995
A_23_P100240 33.3715 A 5.401
A_23_P10025 53.7904 A 6.1165
A_23_P100263 3791.083 P 12.2151

Total number of rows: 41078

Table truncated, full table size 1217 Kbytes.




Supplementary file Size Download File type/resource
GSM592131.txt.gz 2.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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