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Sample GSM947862 Query DataSets for GSM947862
Status Public on Sep 01, 2012
Title late_torpor_04-38
Sample type RNA
 
Source name liver, hibernating
Organism Urocitellus parryii
Characteristics tissue: liver
status: late 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 0.474666868
gene0002 34.95400232
gene0003 1.741039096
gene0004 0.459821102
gene0005 2.278063731
gene0026 17.0073805
gene0027 2.730787163
gene0028 2.655704453
gene0029 1.606900075
gene0030 0.843474421
gene0051 0.333926476
gene0052 0.644414458
gene0053 3.147267012
gene0054 0.497468806
gene0055 0.991287822
gene0076 3.380190797
gene0077 1.098460322
gene0078 0.596916328
gene0079 0.724059405
gene0080 1.802669371

Total number of rows: 9600

Table truncated, full table size 195 Kbytes.




Supplementary file Size Download File type/resource
GSM947862_VF_14-LT04-38_GS01_A1-20_110308.txt.gz 631.7 Kb (ftp)(http) TXT
Processed data included within Sample table

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