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Sample GSM892752 Query DataSets for GSM892752
Status Public on Sep 21, 2012
Title 3rd fraction of So series slicing
Sample type RNA
 
Source name 5 micron x 200 sagittal a little oblique slices (1 mm width) of the brain, set 2
Organism Mus musculus
Characteristics strain: C57BL/6J
tissue: brain
gender: male
age: 8 weeks
section type: sagittal oblique plane
mouse id: 2
Growth protocol Mice were grown in pathogen-free conditions.
Extracted molecule total RNA
Extraction protocol RNA was prepared using the Mag-max-96 for Microarrays Total RNA Isolation Kit (Ambion) following the manufacturer's recommendations of the spin column protocol. RNA was quantified using a NanoDrop-1000 spectrophotometer and quality was monitored with the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).
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 RNeasy 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 manufacturer's instructions. On completion of the fragmentation reaction, 250 ul of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Whole Human Genome Oligo Microarrays 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 using the 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 So_03
Data processing The scanned images were analyzed with Feature Extraction Software 9.1 (Agilent) using default parameters (protocol GE1-v1_91) to obtain background subtracted and spatially detrended Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded. Data were normalized using per chip: normalize to 50th percentile.
 
Submission date Mar 09, 2012
Last update date Sep 21, 2012
Contact name Yuko Okamura-Oho
E-mail(s) yoho-tky@umin.ac.jp
Organization name RIKEN
Street address 2-1, Hirosawa
City Wako-shi
State/province Saitama
ZIP/Postal code 351-0198
Country Japan
 
Platform ID GPL7202
Series (1)
GSE36408 Gene expression profiling of the whole mouse brain using transcriptome tomography

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
A_51_P108701 300.9636
A_51_P266695 5.311734
A_51_P314264 67.74016
A_51_P425962 271.6591
A_51_P237076 157.12881
A_51_P276939 1.7273753
A_51_P377760 4.272473
A_51_P296940 5.479454
A_52_P50107 31.540907
A_51_P481978 13.007459
A_52_P648203 6.0048685
A_52_P1092136 1.3841481
A_52_P139093 19.191607
A_51_P296975 1.6883534
A_51_P348672 14.1948805
A_51_P513424 17.479733
A_52_P139097 80.463455
A_52_P674759 31.623064
A_51_P479786 2.6616263
A_51_P386189 74.348816

Total number of rows: 36558

Table truncated, full table size 828 Kbytes.




Supplementary file Size Download File type/resource
GSM892752_Processed-US14702386_251486810737_S01_GE1-v5_91_0806_1_1.txt.gz 1.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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