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Sample GSM947860 Query DataSets for GSM947860
Status Public on Sep 01, 2012
Title early_torpor_2000-43
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 0.46678648
gene0002 41.23246123
gene0003 1.989003675
gene0004 0.160849801
gene0005 1.325088486
gene0026 20.85211795
gene0027 1.394383434
gene0028 1.562065131
gene0029 1.119600472
gene0030 0.717376173
gene0051 0.294747525
gene0052 0.637720897
gene0053 1.170629104
gene0054 0.441544492
gene0055 0.515773494
gene0076 3.720968035
gene0077 0.945098719
gene0078 0.458983673
gene0079 0.682844565
gene0080 1.244866563

Total number of rows: 9600

Table truncated, full table size 195 Kbytes.




Supplementary file Size Download File type/resource
GSM947860_VF_12-ET2000-43_GS01_A1-07_110308.txt.gz 635.4 Kb (ftp)(http) TXT
Processed data included within Sample table

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