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Sample GSM149931 Query DataSets for GSM149931
Status Public on Dec 15, 2006
Title MCF7_inhibitor_HRG_U0126_15min
Sample type RNA
 
Source name breast epithelial cell, adherent, HRG, U0126, 15min
Organism Homo sapiens
Characteristics Cell line: MCF-7 (Obtained from ATCC (American Type Culture Collection)), Organ: mammary gland; breast, Cell type: epithelial, Disease: adenocarcinoma, Derived from metastatic site: pleural effusion, Age: 69 years adult, Gender: female, Ethnicity: Caucasian
Treatment protocol Before treatments, medium were changed with serum-free medium again and incubated at 37C for 2 hours. Followed by incubation, added each ligand and incubated for each time.
Growth protocol Prior to the growth factor (GF) treatment, cells were serum starved for 16-18 hours with serum-free DMEM medium and incubated at 37C/5% CO2. The medium was again changed 2 hr prior to the GF treatment. The inhibitor, U0126 (a MEK inhibitor) was added to 20 min prior to the GF treatment.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using TRIzol reagent (Invitrogen) and then purified using QIAGEN Rneasy kit.
Label biotin
Label protocol Standard Affymetrix Protocols (Affymetrix GeneChip Expression Analysis Technical Manual) was used. Complete protocal can be found manufacturer's web site (http://www.affymetrix.com/support/technical/manual/expression_manual.affx) (section2, chapter1-p13-18, & 2.1.p32-33,p36-40)
 
Hybridization protocol Standard Affymetrix Protocols (Affymetrix GeneChip Expression Analysis Technical Manual) was used. Complete protocal can be found manufacturer's web site (http://www.affymetrix.com/support/technical/manual/expression_manual.affx) (section2, 2.2.p3-8 & 2.3.p3-14)
Scan protocol GeneChips were scanned using the GeneChip Scanner 3000 with default parameter.
Description Early gene expression (up to 90min) induced by growth hormone stimulation with a MEK inhibitor.
Data processing The data were analyzed with GeneChip Operating System (GCOS) (ver.1.2) using Affymetrix default analysis settings and global scaling as normalization method. The Single-Array Expression Analysis function was used and the trimmed mean target intensity of each array was arbitrarily set to 500.
 
Submission date Dec 13, 2006
Last update date Aug 28, 2018
Contact name Mariko Okada
E-mail(s) [email protected]
Organization name RIKEN RCAI
Lab Laboratory for Cellular Systems Modeling
Street address W518, 1-7-22, Suehiro-cho, Tsurumi-ku
City Yokohama
ZIP/Postal code 230-0045
Country Japan
 
Platform ID GPL570
Series (1)
GSE6521 MCF7 inhibitor
Relations
Reanalyzed by GSE64985
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE GCOS calculated signal intensities
ABS_CALL the call in an absolute analysis that indicates if the transcript was present (P), absent (A) or marginal (M)

Data table
ID_REF VALUE ABS_CALL
1007_s_at 4647.6 P
1053_at 725.6 P
117_at 149.9 A
121_at 818.1 P
1255_g_at 66.4 A
1294_at 157.4 P
1316_at 177.8 P
1320_at 164.1 A
1405_i_at 12.4 A
1431_at 97.3 P
1438_at 399.2 P
1487_at 1184.1 A
1494_f_at 33.1 A
1552256_a_at 2385.3 P
1552257_a_at 1354.1 P
1552258_at 106.3 A
1552261_at 62.2 A
1552263_at 103.7 P
1552264_a_at 225.2 M
1552266_at 127.0 P

Total number of rows: 54675

Table truncated, full table size 986 Kbytes.




Supplementary file Size Download File type/resource
GSM149931.CEL.gz 4.3 Mb (ftp)(http) CEL
GSM149931.EXP.gz 398 b (ftp)(http) EXP

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