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Sample GSM304782 Query DataSets for GSM304782
Status Public on Jan 13, 2009
Title F10T1R1
Sample type RNA
 
Source name Family 10 Time 1
Organism Magallana gigas
Characteristics Gill
Low-surviving family
2.5 years of age
1 hour 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 10 Time 1 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) [email protected]
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 6.959343965
5 6.762413938
8 9.629694056
9 9.481828451
10 7.337274707
11 7.338780343
14 8.184665676
15 8.165178737
16 8.796658471
17 8.529773027
18 8.456389123
19 8.444784334
20 7.520294114
21 6.074741925
24 8.526203584
27 8.57465366
30 8.429581015
31 8.470946556
32 6.715975276
33 6.717546924

Total number of rows: 3362

Table truncated, full table size 55 Kbytes.




Supplementary file Size Download File type/resource
GSM304782.txt.gz 2.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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