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Sample GSM727511 Query DataSets for GSM727511
Status Public on May 04, 2012
Title hippo_msn_rep5
Sample type RNA
 
Source name hippo_MSN
Organism Mus musculus
Characteristics mouse line: Madison (MSN)
gender: male
age: adult
tissue: macrodissected hippocampus
behavioral phenotype: manic
Treatment protocol Prior to RNA extraction, all mice were euthanized by decapitation under deep isofluorane anaesthesia in accordance with UW-Madison IACUC guidelines, and hippocampi were macrodissected and frozen immediately on dry ice. Tissue was stored for no more than 12 weeks prior to extraction.
Growth protocol Madison (MSN) mice were selectively bred to display a manic phenotype; hsd:ICR (ICR) mice are the outbred ancestral strain from which MSN mice were derived. Each line has been maintained in our lab for many generations. All mice used were male mice, and all mice were approximately the same age.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the Aurum Total RNA Fatty and Fibrous Tissue Kit (Bio-Rad, Hercules, CA, USA), which uses a guanidinium thiocyanate-phenol-chloroform extraction followed by a spin column cleanup and purification. RNA purity and concentration were assessed using a NanoDrop spectrophotometer, and RNA integrity was assessed using an RNA Pico Chip on an Agilent BioAnalyzer 2100.
Label biotin
Label protocol 400ng of each total RNA sample were labeled with an Ambion GeneChip WT Expression Kit (Ambion, Austin, TX, USA) according to the manufacturer's specifications.
 
Hybridization protocol Samples were hybridized to arrays at 45C for 16 hours following procedures outlined in the GeneChip WT Terminal Labeling and Hybridization Use Manual , Rev. 4.
Scan protocol Arrays were scanned on the Affymetrix GC3000 G7 scanner, and data were extracted and processed using Affymetrix Command Console v3.1.1.1229.
Description Madison (MSN) mice are a line derived from the outbred ICR ancestral line that displays a manic phenotype relative to ICR. MSN mice spend significantly more time moving and significantly less time resting than the ancestral ICR line.
Data processing Raw array data were normalized and summarized at the probeset level using Affymetrix Power Tools v1.12.0 with default settings for PLIER with GC-bin background correction. Summarized data were analyzed using limma for BioConductor v3.6.9.
 
Submission date May 20, 2011
Last update date May 05, 2012
Contact name Michael C. Saul
E-mail(s) michael.saul@jax.org
Organization name The Jackson Laboratory
Lab Chesler Lab
Street address 600 Main St
City Bar Harbor
State/province ME
ZIP/Postal code 04609
Country USA
 
Platform ID GPL6246
Series (1)
GSE29417 A new mouse model for mania shares genetic correlates with human bipolar disorder.

Data table header descriptions
ID_REF
VALUE PLIER signal intensity

Data table
ID_REF VALUE
10338001 4738.79161
10338002 306.82271
10338003 1778.99687
10338004 1013.99166
10338005 5.33589
10338006 7.47273
10338007 16.04705
10338008 40.10558
10338009 854.59746
10338010 4.70764
10338011 147.46705
10338012 6.33327
10338013 3.3651
10338014 4.19538
10338015 4.50447
10338016 605.58564
10338017 10360.43966
10338018 292.31291
10338019 94.16204
10338020 570.92072

Total number of rows: 35556

Table truncated, full table size 655 Kbytes.




Supplementary file Size Download File type/resource
GSM727511.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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