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Sample GSM231609 Query DataSets for GSM231609
Status Public on Sep 01, 2009
Title SH-SY5Y(ATCC)_RA_inhibiter_LY294002_6h_rep1
Sample type RNA
 
Source name neuroblastoma cell, retinoic acid (RA), LY294002, 6hour
Organism Homo sapiens
Characteristics Cell line: SH-SY5Y (CRL-2266, obtained from ATCC (American Type Culture Collection Cultures))
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.
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.
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.
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.)
 
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.).
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.
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.
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.).
 
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
Fax (+81) 45 503 9176
URL http://hgp.gsc.riken.go.jp/index.php/Main_Page
Organization name RIKEN GSC
Department Computatinal and Experimental Systems Biology Group
Lab Genome Annotation and Comparative Analysis Team
Street address 1-7-22, Suehiro-cho, Tsurumi-ku
City Yokohama
State/province Kanagawa
ZIP/Postal code 230-0045
Country Japan
 
Platform ID GPL570
Series (1)
GSE9169 Gene expression during neuronal differentiation in two subtypes of SH-SY5Y

Data table header descriptions
ID_REF
VALUE Signal
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 827.258 P 0.000581214
AFFX-BioB-M_at 964.047 P 4.42873e-05
AFFX-BioB-3_at 734.35 P 5.16732e-05
AFFX-BioC-5_at 2454.25 P 5.16732e-05
AFFX-BioC-3_at 3212.92 P 4.42873e-05
AFFX-BioDn-5_at 5868.88 P 4.42873e-05
AFFX-BioDn-3_at 11256.7 P 6.02111e-05
AFFX-CreX-5_at 26028.7 P 5.16732e-05
AFFX-CreX-3_at 31743.5 P 4.42873e-05
AFFX-DapX-5_at 421.141 P 7.00668e-05
AFFX-DapX-M_at 778.953 P 0.00141043
AFFX-DapX-3_at 947.018 P 8.14279e-05
AFFX-LysX-5_at 68.4253 P 0.00844047
AFFX-LysX-M_at 108.922 M 0.0542134
AFFX-LysX-3_at 256.068 P 7.00668e-05
AFFX-PheX-5_at 51.8545 P 0.000445901
AFFX-PheX-M_at 133.611 P 0.00499819
AFFX-PheX-3_at 158.518 P 0.0061833
AFFX-ThrX-5_at 140.389 P 0.00159257
AFFX-ThrX-M_at 174.659 P 0.000445901

Total number of rows: 54675

Table truncated, full table size 1643 Kbytes.




Supplementary file Size Download File type/resource
GSM231609.CEL.gz 4.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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