NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM875047 Query DataSets for GSM875047
Status Public on Feb 15, 2012
Title BA02_bone_hibernating_N05-034
Sample type RNA
 
Source name bone, hibernating
Organism Ursus americanus
Characteristics tissue type: bone
gender: male
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). Skeletal muscle tissue was treated by proteinase K and RNA was extracted by using RNeasy Fibrous Tissue Kit (Qiagen). All 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 bone tissue from hibernating black bear
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 Feb 14, 2012
Last update date Feb 15, 2012
Contact name Haifang Wang
Organization name Shanghai institute for biology science
Department CAS-MPG Partner institute for Computational Biology
Street address 320 yueyang road
City Shanghai
ZIP/Postal code 200031
Country China
 
Platform ID GPL13263
Series (1)
GSE35796 Preservation of bone mass and structure in hibernating black bears (Ursus americanus) through elevated expression of anabolic genes

Data table header descriptions
ID_REF
VALUE normalized expression value

Data table
ID_REF VALUE
1 1.417
2 2.269
3 3.225
4 0.315
5 0.601
6 1.138
7 0.616
8 0.812
9 4.591
10 0.949
11 2.089
12 6.688
13 1.308
14 1.160
15 1.895
16 6.618
17 307.329
18 0.002
19 0.407
20 0.262

Total number of rows: 9600

Table truncated, full table size 102 Kbytes.




Supplementary file Size Download File type/resource
GSM875047.txt.gz 668.9 Kb (ftp)(http) TXT
Processed data included within Sample table

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