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Sample GSM1547415 Query DataSets for GSM1547415
Status Public on Jan 05, 2015
Title Soleus male 2
Sample type RNA
 
Source name normal soleus muscle
Organism Rattus norvegicus
Characteristics tissue: soleus muscle
Sex: male
strain: Han Wistar-derived rats (AlpkHsdBrlHan:WIST)
Treatment protocol Rats were humanely killed at a designated establishment by halothane inhalation, which is an appropriate method under Schedule 1 of the Act.Organs and tissues were removed and cleaned of extraneous tissue by a 5-person necropsy team within 5 min of death, then frozen in liquid nitrogen. Pancreas was prioritized for rapid freezing, since its mRNA is known to be particularly vulnerable to degredation. Tissue samples from each animal weighing 100-250 mg were taken from frozen samples and homogenized immediately in RNeasy lysis buffer. Care was taken to ensure samples were taken consistently from the same region of tissue for each individual, and that they were representative of the whole organ (e.g. radial segments of kidney were taken from the equator in each case).
Growth protocol Rats were housed 2-3 per cage
Extracted molecule total RNA
Extraction protocol RNA was purified from lysates using Qiagen RNeasy mini columns according to the manufacturer’s instructions. Nucleic acid (RNA) purity was determined according to the 260/280nM absorbance ratio using a Nanodrop-1000 (Thermo Scientific). Samples were accepted only if the ratio fell between 1.8 and 2.2. Otherwise, RNA was re-extracted from new samples of frozen tissue. RNA integrity was assessed using the 2100 Bioanalyser (Agilent). Samples with an RNA integrity number (RIN) <7 were rejected, and re-processed.
Label biotin
Label protocol cDNA, biotin-labelled cRNA and fragmented hybridization probes were prepared using the Affymetrix IVT kit (Affymetrix CA.).
 
Hybridization protocol Hybridization mixes including control oligos and biotin-labelled cRNA were prepared following the Affymetrix protocol. Hybridisation to Affymetrix RAE230_2 rat genechips® was carried out overnight at 45oC rotating at 60 rpm. Bound biotinylated probes were revealed with strptavidin-phycoerythrin complex according to the Affymetrix protocol.
Scan protocol Scanning was carried out with an Affymetric 3000 scanner using the RAE_230_V2 protocol
Data processing R bioconductor was used for primary analysis, analysis was using GC-RMA-s
 
Submission date Nov 17, 2014
Last update date Jan 05, 2015
Contact name Russell Huby
Organization name AstraZeneca
Street address Alderley Park
City Macclesfield
State/province Cheshire
ZIP/Postal code SK10 4TG
Country United Kingdom
 
Platform ID GPL1355
Series (1)
GSE63362 Identification of sexually dimorphically expressed genes in rat tissues

Data table header descriptions
ID_REF
VALUE Data in the matrix table are log2 GC-RMA values

Data table
ID_REF VALUE
1367452_at 10.729709
1367453_at 10.347759
1367454_at 9.967408
1367455_at 11.799092
1367456_at 11.805099
1367457_at 10.057062
1367458_at 6.2902265
1367459_at 11.657672
1367460_at 11.909628
1367461_at 9.366741
1367462_at 11.334495
1367463_at 11.851395
1367464_at 10.056178
1367465_at 9.372919
1367466_at 9.696333
1367467_at 11.768726
1367468_at 8.821138
1367469_at 12.619985
1367470_at 10.420389
1367471_at 9.64634

Total number of rows: 31042

Table truncated, full table size 626 Kbytes.




Supplementary file Size Download File type/resource
GSM1547415_NRTP_-_2202_-_Soleus.CEL.gz 2.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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