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Sample GSM333312 Query DataSets for GSM333312
Status Public on May 01, 2009
Title Pineal_LD_ZT10
Sample type RNA
Source name pineal at ZT10, 12-h light/12-h dark cycle
Organism Danio rerio
Characteristics Tg(aanat2:EGFP)Y8 transgenic zebrafish
Age: adult (3-6 months)
Gender: males and females
Treatment protocol Fish were anesthetized in 1.5 mM Tricane (Sigma) and sacrificed by decapitation, and pineal glands were removed under a fluorescent dissecting microscope. 12 pineal glands were collected and pooled at each time point and at each light condition.
Growth protocol Adult zebrafish were raised in a light- and temperature-controlled recirculation water system under a 12-h light/12-h dark cycle at 28 ┬░C and fed twice a day.
Extracted molecule total RNA
Extraction protocol Extraction of total RNA was performed according to the manufacturer's instructions (RNeasy, Qiagen).
Label biotin
Label protocol Double-strand cDNA was generated from 10-100 ng of mRNA by using a T7-linked oligo(dT) primer (Affymetrix). After second-strand synthesis, in vitro transcription was performed with MEGAscript® T7 Kit (Ambion, Inc.). The cRNA (600ng) was then used for second cycle first-strand cDNA (Affymetrix) by using a T7-linked oligo(dT) primer (Affymetrix). After 2nd cycle - second-strand synthesis, in vitro transcription was again performed; this time biotinylated UTP and CTP (Affymetrix) were incorporated in the cRNA, resulting in approximately 1800-fold amplification of labeled RNA.
Hybridization protocol The target cRNA generated from each sample was fragmented and 15 micogram of the fragmented cRNA was added to the hybridization cocktail which includes in addition to the fragmented target, probe array controls (pre-mixed biotin-labeled bioB, bioC, bioD and cre, in staggered concentrations, ready to be added directly to the hybridization cocktail. These controls facilitate monitoring of the hybridization process for troubleshooting), BSA, and herring sperm DNA. It was then hybridized to the probe array during a 16-hour incubation at 45 deg (C). The array was then washed and stained on the Affymetrix fluidic station (using Streptavidin-Phycoerythrin which binds to the biotinylated UTP and CTP incorporated previously in the hybridized cRNA).
Scan protocol The stained array was scanned on the Affymetrix scanner (450).
Description Gene expression data from zebrafish pineal
Data processing The GCOS (Gene Operating System) generates the numerical data from the scanned intensities using the MAS 5 software (MicroArray suite 5.0; Affymetrix).
Submission date Oct 14, 2008
Last update date Oct 14, 2008
Contact name Yoav Gothilf
Phone +972-3-640-6329
Fax +972-3-640-6329
Organization name Tel Aviv University
Department Neurobiology, Faculty of Life Sciences
Lab Gothilf
Street address Sherman Building, Room 405
City Tel Aviv
ZIP/Postal code 69978
Country Israel
Platform ID GPL1319
Series (1)
GSE13196 Expression data from zebrafish pineal gland

Data table header descriptions
VALUE MAS5.0 signal intensity

Data table
Dr.9890.1.A1_at 3324.4
Dr.14317.1.A1_at 2700.6
AFFX-DapX-3_at 1251
Dr.12469.1.S1_at 5274.5
Dr.9901.1.S1_at 2097.3
Dr.9841.1.A1_at 5054.5
AFFX-r2-Bs-dap-3_at 805
Dr.9908.1.A1_at 8235.8
Dr.12466.1.A1_s_at 3441.9
Dr.11215.1.A1_at 7066.7
Dr.14325.1.S1_at 1332.6
AFFX-r2-Bs-dap-M_at 409.3
Dr.8142.1.S1_at 3781.2
Dr.12451.2.A1_at 5525.2
Dr.20055.1.A1_at 3949.4
Dr.11072.1.A1_at 2512.3
Dr.23415.1.A1_at 7537.5
Dr.12592.1.S1_at 677.4
Dr.11183.1.A1_at 4431.1
Dr.9899.1.S2_at 3750.4

Total number of rows: 15617

Table truncated, full table size 332 Kbytes.

Supplementary file Size Download File type/resource
GSM333312.CEL.gz 1.9 Mb (ftp)(http) CEL
Raw data provided as supplementary file
Processed data included within Sample table

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