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Status |
Public on Dec 09, 2006 |
Title |
MCF7_dose_EGF_1.0nM_10min |
Sample type |
RNA |
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Source name |
breast epithelial cell, adherent, EGF, 1.0nM, 10min
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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
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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.
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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.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated using TRIzol reagent (Invitrogen) and then purified using QIAGEN Rneasy kit.
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Label |
biotin
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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)
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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)
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Scan protocol |
GeneChips were scanned using the GeneChip Scanner 3000 with default parameter.
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Description |
Early gene expression (up to 90min) induced by growth hormone stimulation.
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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.
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Submission date |
Dec 06, 2006 |
Last update date |
Dec 08, 2006 |
Contact name |
Mariko Okada |
E-mail(s) |
marikoh@rcai.riken.jp
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Organization name |
RIKEN RCAI
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Lab |
Laboratory for Cellular Systems Modeling
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Street address |
W518, 1-7-22, Suehiro-cho, Tsurumi-ku
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City |
Yokohama |
ZIP/Postal code |
230-0045 |
Country |
Japan |
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Platform ID |
GPL571 |
Series (1) |
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