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Sample GSM977874 Query DataSets for GSM977874
Status Public on Dec 04, 2013
Title dentate gyrus-subgranular zone-30daysRunning, repAT1
Sample type RNA
 
Source name Subgranular zone (inner granule cell layer) from a mouse allowed access to running wheel for 30 days
Organism Mus musculus
Characteristics strain: C57BL/6
age: 10-11 week old
Sex: male
tissue: brain
region: dentate gyrus-subgranular zone
days_running: 30
animal: AT1
Treatment protocol Brains were quickly removed, flash-frozen in OCT mounting medium in a dry ice-isopentantane slurry, and stored at -80C until use. 12μm thin cryostat sections were stained with cresyl violet, rapidly dehydrated through xylenes, and stored until use a vacuum dessicator. An Arcturus PixCell II machine (Arcturus, Mountain View, CA) was used to isolate 2-3 cell thick bands from both the inner and outer portions of the dentate granule cell layer.
Extracted molecule total RNA
Extraction protocol Total RNA was purified from the laser captured tissue using the Absolutely RNA Nanoprep Kit (Stratagene, La Jolla, CA), and RNA yield was assessed using the RiboGreen RNA Quantitation Reagent (Molecular Probes Inc, Eugene, OR). RNA from three groups of animals (no running, 4 days of running, 30 days of running), consisting of 3 animals each, was isolated independently and amplified separately.
Label biotin
Label protocol 5ng total RNA starting material was amplified using the MessageAmp aRNA Kit (Ambion Inc, Austin, TX). This method utilizes reverse transcription with T7 RNA Polymerase. The first and second rounds of the kit were performed per the manual, with an additional third round identical to the second round except that the in vitro transcription step utilized the Enzo BioArray High Yield RNA Transcript Labeling Kit (Affymetrix, Santa Clara, CA).
 
Hybridization protocol 15μg of biotinylated aRNA was fragmented and hybridized to Affymetrix MG-U74Av2 arrays.
Scan protocol Gene chips were scanned following the manufactures protocol.
Description Gene expression data from 10- to 11-week-old C57BL/6 male mice
Data processing Initial data analysis and normalization were done using the Affymetrix Expression Console using two algorithms: Robust Multichip Analysis (RMA) and Probe Logarithmic Intensity Error Estimation (PLIER) using the minus mismatch option (-MM). Note that an additional filtering step to remove the effect of running was performed in the larger cross-species study, using ComBat (www.bu.edu/jlab/wp-assets/ComBat).
 
Submission date Jul 27, 2012
Last update date Dec 04, 2013
Contact name Jeremy Miller
E-mail(s) [email protected]
Organization name Allen Institute for Brain Science
Street address 615 Westlake Ave N
City Seattle
State/province WA
ZIP/Postal code 98109
Country USA
 
Platform ID GPL81
Series (1)
GSE39697 Molecular Signatures of Neurogenesis in the Hippocampal Subgranular Zone of Rodents

Data table header descriptions
ID_REF
VALUE RMA normalized signal intensity

Data table
ID_REF VALUE
100001_at 31.49
100002_at 121.01
100003_at 290.80
100004_at 65.85
100005_at 59.09
100006_at 112.11
100007_at 62.17
100009_r_at 619.96
100010_at 31.47
100011_at 103.85
100012_at 256.00
100013_at 30.06
100014_at 78.15
100015_at 28.04
100016_at 34.02
100017_at 23.27
100018_at 178.65
100019_at 101.16
100020_at 75.73
100021_at 21.73

Total number of rows: 12488

Table truncated, full table size 199 Kbytes.




Supplementary file Size Download File type/resource
GSM977874_JN03021101.CEL.gz 2.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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