NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM947858 Query DataSets for GSM947858
Status Public on Sep 01, 2012
Title early_torpor_04-15
Sample type RNA
 
Source name liver, hibernating
Organism Urocitellus parryii
Characteristics tissue: liver
status: early torpor
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from frozen tissues stored at -80 °C by grinding in liquid nitrogen with mortar and pestle and using RNeasy Kit (Qiagen). RNA samples were processed by DNase I (Qiagen) treatment. For cDNA library construction, mRNA was selected from total RNA with the oligo(dT) cellulose by the use of Poly(A) Purist Kit (Ambion).
Label 33P
Label protocol Samples of total RNA were linearly amplified with Illumina TotalPrep RNA Amplification Kit (Ambion), and 1.6 μg of the amplified RNA was labeled with 65 μCi of [33P]dCTP. All RNA samples were amplified, labeled and hybridized in the same batch.
 
Hybridization protocol The hybridization was carried out for 18 hours at 42 °C in 4 ml of MicroHyb buffer (Invitrogen). Filters were rinsed at room temperature with 2× SSC/1% SDS to remove residual probe and MicroHyb solution and then transferred to preheated wash solutions in a temperature-controlled shaking water bath. Filters were washed twice for 30 min in 1.5 l of 2× SSC/1% SDS at 50 °C and then once for 30 min in 1.5 l of 0.5× SSC/1% SDS at 55 °C.
Scan protocol Filters were then exposed to phosphorimager screens for four days and scanned at 50-µm resolution in a Storm Phosphorimager.
Description liver tissue from hibernating arctic ground squirrel
Data processing Image analysis was performed with the ImaGene program (Biodiscovery). Only nonempty spots with signal median density exceeding double background median in all individuals were included in the analysis. Background corrected signal was obtained by subtracting local background median density from signal median density. Background corrected signals were divided by their median on the array to obtain the normalized median densities representing the normalized expression values.
 
Submission date Jun 13, 2012
Last update date Sep 01, 2012
Contact name Yichi Xu
E-mail(s) [email protected]
Organization name MSKCC
Street address 1275 York Avenue
City New York
State/province NY
ZIP/Postal code 10065
Country USA
 
Platform ID GPL15674
Series (1)
GSE38700 Analysis of molecular signatures in mammalian hibernation

Data table header descriptions
ID_REF
VALUE The background-subtracted signals were normalized by median divided

Data table
ID_REF VALUE
gene0001 0.402278221
gene0002 28.44683554
gene0003 1.001368567
gene0004 0.283428521
gene0005 2.207531833
gene0026 21.15381951
gene0027 1.911630933
gene0028 2.196362013
gene0029 1.8779882
gene0030 0.871551472
gene0051 0.8318536
gene0052 0.896839472
gene0053 2.966528888
gene0054 0.579267814
gene0055 1.019704975
gene0076 3.751904018
gene0077 0.503837582
gene0078 0.520308163
gene0079 0.62838032
gene0080 1.725045656

Total number of rows: 9600

Table truncated, full table size 195 Kbytes.




Supplementary file Size Download File type/resource
GSM947858_VF_10-ET04-15_GS01_A1-06_110308.txt.gz 633.8 Kb (ftp)(http) TXT
Processed data included within Sample table

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