NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM977901 Query DataSets for GSM977901
Status Public on Dec 31, 2012
Title muscle_Wt_8wk_rep3
Sample type RNA
 
Source name quadriceps_muscle_Wt_female_8wk_rep3
Organism Mus musculus
Characteristics strain: C57BL/6
tissue: quadriceps_muscle
gender: female
age: 8week
Extracted molecule total RNA
Extraction protocol RNA was prepared using the Rneasy lipid tissue mini kit(Quiagen).
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 0.5 ug RNA using the One-Color Low RNA Input Linear Amplification PLUS kit (Agilent) according to the manufacturer's instructions, followed by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol 1.5 ug of Cy3-labelled cRNA (specific activity >10.0 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 250 ml containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 250 ml of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Whole Human Genome Oligo Microarrays (G4112A) for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then dried immediately by brief centrifugation.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2505B) using one color scan setting for 1x44k array slides (Scan Area 61x21.6 mm, Scan resolution 10um, Dye channel is set to Green and Green PMT is set to 100%).
Description quadriceps_muscle_Wt_female_8wk_rep3
Data processing The scanned images were analyzed with Feature Extraction Software 9.1 (Agilent) using default parameters (protocol GE1-v1_91 and Grid: 012391_D_20060331) to obtain background subtracted and spatially detrended Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded.
 
Submission date Jul 27, 2012
Last update date Dec 31, 2012
Contact name Aika Nojima
E-mail(s) [email protected]
Organization name Chiba univeersity
Street address 1-8-1
City Chiba
ZIP/Postal code 260-8670
Country Japan
 
Platform ID GPL7202
Series (1)
GSE39699 gene expression signatures of Akt1 +/- mice at 8weeks and 35weeks

Data table header descriptions
ID_REF
VALUE log2 Normalized signal intensity

Data table
ID_REF VALUE
GE_BrightCorner 6.11467
DarkCorner -7.450307
A_52_P616356 -7.2937083
A_52_P580582 -4.292886
A_52_P403405 -1.5706596
A_52_P819156 -3.817676
A_51_P331831 -3.4038367
A_51_P430630 -7.275166
A_52_P502357 -7.274822
A_52_P299964 -6.1943045
A_51_P356389 -5.807191
A_52_P684402 0.5069628
A_51_P414208 -7.279484
A_51_P280918 0.34286594
A_52_P613688 -4.529517
A_52_P258194 -3.195881
A_52_P229271 -3.887165
A_52_P214630 -2.0888405
A_52_P579519 -2.1093655
A_52_P979997 -7.3043995

Total number of rows: 41267

Table truncated, full table size 944 Kbytes.




Supplementary file Size Download File type/resource
GSM977901_Rn895.txt.gz 7.9 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap