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Sample GSM304800 Query DataSets for GSM304800
Status Public on Jan 13, 2009
Title F25T3R1
Sample type RNA
 
Source name Family 25 Time 3
Organism Magallana gigas
Characteristics Gill
High-surviving family
2.5 years of age
3 hours after heat shock
Treatment protocol heat shocked 40C, 1 hour
Extracted molecule total RNA
Extraction protocol Each sample contaiend 50 mg gill from three individuals of each family. Total RNA were extracted using the Qiagen miniprep system and on-column DNAse treatment. Total RNA were used as template for synthesizing antisense RNA using the Amino Allyl MessageAmp™ Kit (Ambion, Inc., Austin, TX). Each reaction included RNA standards: 100 ng chlorophyll A/B binding protein (Genbank #CO059871) RNA, 10 ng photosystem core protein (Genbank #CO062297) RNA, 1 ng flavodoxin (Genbank #CO065421) RNA, and 0.1 ng photolyase (Genbank #CO064781) RNA.
Label Cy3
Label protocol 1 microgram of antisense RNA was labeled with Cy3 dye according to the protocol for the Amino Allyl MessageAmp™ Kit (Ambion, Inc., Austin, TX).
 
Hybridization protocol Each slide hybridized with 90-μl mixture containing 20 μg of Cy3-coupled aRNA in hybridization buffer [50% formamide, 2.4% SDS, 4xSSPE, 2.5x Denhardt’s solution, plus 1 µg Cot-DNA and 1 µg polydATP]. Hybridizations were conducted at 50°C in a humidified hybridization oven (Boekel Inslide-Outtm, Boekel, Festerville, PA) for 12 h.
Scan protocol ScanArray Express (Perkin Elmer, Boston, MA) microarray scanner, 70% PMT gain and 90% laser power.The QuantArray software package (Perkin Elmer, Boston, MA) was used to acquire raw fluorescence data, background, and spot quality information from the scanned images using the included Histogram spot segmentation method. Each spot image was visually inspected for overall quality, and damaged spots were excluded prior to statistical analysis.
Description Family 25 Time 3 Replicate 1
Data processing We transformed the entire dataset using a variance stabilization normalization method (vsn; Huber et al. 2002). All spots were included in the transformation. Spot pairs were excluded whose average intensity across the 60 slides was less than 6 for at least 1 of the sampling times, and we excluded all unsequenced spots. We omitted flagged spots prior to statistical analysis.
 
Submission date Jul 10, 2008
Last update date Jan 13, 2009
Contact name Marine Genomics
E-mail(s) info@marinegenomics.org
Phone 8437628869
URL http://www.marinegenomics.org
Organization name Medical University South Carolina
Street address 331 Ft. Johnson Road
City Charleston
State/province SC
ZIP/Postal code 29412
Country USA
 
Platform ID GPL3994
Series (1)
GSE12070 Transcriptome profiling of Pacific oyster Crassostrea gigas families that differ in tolerance of heat shock

Data table header descriptions
ID_REF
VALUE vsn-transformed signal intensity

Data table
ID_REF VALUE
4 6.869824348
5 6.910283361
8 9.397708682
9 9.518447545
10 7.630520041
11 7.307831977
14 8.798104465
15 8.592931885
16 8.639843023
17 8.693219634
18 8.580517487
19 8.668281242
20 7.098949654
21 6.283209591
24 8.360635506
27 8.772220887
30 8.184957195
31 8.105263333
32 6.900698588
33 6.874919675

Total number of rows: 3362

Table truncated, full table size 56 Kbytes.




Supplementary file Size Download File type/resource
GSM304800.txt.gz 2.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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