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Status |
Public on Sep 01, 2009 |
Title |
SH-SY5Y(ATCC)_RA_inhibiter_LY294002_6h_rep1 |
Sample type |
RNA |
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Source name |
neuroblastoma cell, retinoic acid (RA), LY294002, 6hour
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Organism |
Homo sapiens |
Characteristics |
Cell line: SH-SY5Y (CRL-2266, obtained from ATCC (American Type Culture Collection Cultures))
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Treatment protocol |
SH-SY5Y-A cells were seeded in laminin coated culture dishes (BioCoat Laminin Cellware; BD Biosciences) for 1 day and then transferred to a medium containing 10 μM of RA in the presence of LY294002 (10 μM) for five days.
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Growth protocol |
Tissue culture cells were maintained in D-MEM/F12 1:1 mixture supplemented with 15% FBS (Fetal Bovine Serum) and 1% NEAA (Non-essential amino acid) in a 5% CO2 humidified incubator at 37oC. The culture medium was changed twice a week.
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Extracted molecule |
total RNA |
Extraction protocol |
Total cellular RNA was extracted from the cells at specific intervals using the RiboPure Kit (Ambion, An Applied Biosystems Business, Austin, TX, USA) according to the manufacturer’s instructions.
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Label |
biotin
|
Label protocol |
First-strand cDNA was synthesized using 5 μg of total RNA and the GeneChip One-cycle cDNA Synthesis Kit (Affymetrix, Inc.). Biotin-labeled cRNA was generated by the GeneChip IVT labeling Kit (Affymetrix, Inc.)
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Hybridization protocol |
Biotin-labeled cRNA was applied on the Human Genome U133 Plus 2.0 Array (Affymetrix, Inc.) and then hybridized at 45oC for 17 h in a GeneChip Hybridization Oven (Affymetrix, Inc.).
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Scan protocol |
Washing, staining and scanning of the array were performed using the GeneChip Wash and Stain Kit and a GeneChip Scanner 3000 (Affymetrix, Inc.), respectively.
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Description |
Sampling of RNA was performed at six different time points (0h, 6h, 1d, 2d, 3d, and 5d, respectively) under RA inducible conditions in the presence of Ly294002.
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Data processing |
The average signal intensity for all probes was initially tuned to 500 as global scaling and individual signal intensities were evaluated by detection call (present/marginal/absent) using the Affymetrix Micro Array Suite 5.0 (MAS 5.0) software (Affymetrix, Inc.).
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Submission date |
Sep 26, 2007 |
Last update date |
Aug 14, 2011 |
Contact name |
Tadayuki Takeda |
E-mail(s) |
[email protected]
|
Phone |
(+81) 45 503 9286
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Fax |
(+81) 45 503 9176
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URL |
http://hgp.gsc.riken.go.jp/index.php/Main_Page
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Organization name |
RIKEN GSC
|
Department |
Computatinal and Experimental Systems Biology Group
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Lab |
Genome Annotation and Comparative Analysis Team
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Street address |
1-7-22, Suehiro-cho, Tsurumi-ku
|
City |
Yokohama |
State/province |
Kanagawa |
ZIP/Postal code |
230-0045 |
Country |
Japan |
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|
Platform ID |
GPL570 |
Series (1) |
GSE9169 |
Gene expression during neuronal differentiation in two subtypes of SH-SY5Y |
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