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Sample GSM1047818 Query DataSets for GSM1047818
Status Public on Dec 22, 2014
Title 30.1-30.1
Sample type RNA
 
Source name Brain, left hemisphere excluding cerebellum, 30min asphyxia on E17, P0
Organism Rattus norvegicus
Characteristics strain: Sprague Dawley
gender: male
tissue: brain (left hemisphere excluding cerebellum)
developmental stage: P0
experimental group: FA
Biomaterial provider Charles River
Treatment protocol RNAlater was added directly after excision of the material, and then the material was snap frozen and stored at -80degrees Celsius.
Growth protocol Dams were given standard rodent food ad libitum. Pups were cared for by foster dams.
Extracted molecule total RNA
Extraction protocol Qiagen RNeasy mini kit, protocol available from www.qiagen.com
Label biotin
Label protocol RNA concentration and purity were determined spectrophotometrically using the NanoDrop ND-1000 (NanoDrop Technologies), and RNA integrity was assessed using a Bioanalyser 2100 (Agilent). Using the Ambion WT Expression Kit, per sample, an amount of 100 ng of total RNA spiked with bacterial poly-A RNA positive controls (Affymetrix) was converted to double-stranded cDNA in a reverse transcription reaction. Next, the sample was converted and amplified to antisense cRNA in an in vitro transcription reaction which was subsequently converted to single-stranded sense cDNA. Finally, samples were fragmented and labeled with biotin in a terminal labeling reaction according to the Affymetrix WT Terminal Labeling Kit.
 
Hybridization protocol A mixture of fragmented biotinylated cDNA and hybridisation controls (Affymetrix) was hybridised on Affymetrix GeneChip Rat Gene 1.0 ST Arrays, followed by staining and washing in a GeneChip® Fluidics Station 450 (Affymetrix) according to the manufacturer's procedures.
Scan protocol To assess the raw probe signal intensities, chips were scanned using a GeneChip® scanner 3000 (Affymetrix).
Data processing Data were normalized using RMA as implemented in the Affy package of Bioconductor. Expression values are represented on a log2-scale.
 
Submission date Dec 03, 2012
Last update date Dec 22, 2014
Contact name Rekin's Janky
E-mail(s) Nucleomics.Bioinformatics@vib.be
Organization name VIB
Department Nucleomics Core
Street address Herestraat 49 Box 816
City Leuven
ZIP/Postal code B-3000
Country Belgium
 
Platform ID GPL6247
Series (1)
GSE42676 Functional genomics in perinatal asphyxia and fetal asphyctic preconditioning in the brain

Data table header descriptions
ID_REF
VALUE RMA signal

Data table
ID_REF VALUE
10700001 11.940420051631
10700003 10.1487180703871
10700004 5.26640052129205
10700005 8.81194940909968
10700013 11.2315392107015
10700014 9.96566309318854
10700020 12.091564310688
10700027 7.38211385993393
10700029 12.9895027156551
10700040 8.9048453285608
10700042 13.0660639565319
10700045 9.89763674917453
10700052 4.32184153058795
10700055 8.797463749607
10700058 13.1527189800123
10700059 4.50558610280185
10700062 9.36212135900311
10700064 6.26540688960059
10700065 7.30296786187662
10700066 4.6864725134153

Total number of rows: 27363

Table truncated, full table size 691 Kbytes.




Supplementary file Size Download File type/resource
GSM1047818_hyb9820.CEL.gz 4.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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