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Sample GSM1047827 Query DataSets for GSM1047827
Status Public on Dec 22, 2014
Title 36.2-36.2
Sample type RNA
 
Source name Brain, left hemisphere excluding cerebellum, control, P0
Organism Rattus norvegicus
Characteristics strain: Sprague Dawley
gender: male
tissue: brain (left hemisphere excluding cerebellum)
developmental stage: P0
experimental group: C
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 11.8471826561792
10700003 9.99506046703272
10700004 5.1987259405941
10700005 8.61450373010087
10700013 10.9994574784837
10700014 9.78471989990076
10700020 12.004216954398
10700027 7.27495115688831
10700029 12.817475367295
10700040 8.8160556495692
10700042 12.9598969127935
10700045 9.54594906922448
10700052 4.29747757895961
10700055 8.66116170378693
10700058 13.0990074809832
10700059 4.47833765620076
10700062 9.25730533326396
10700064 6.02624898621771
10700065 7.15431181143649
10700066 4.65017863245108

Total number of rows: 27363

Table truncated, full table size 691 Kbytes.




Supplementary file Size Download File type/resource
GSM1047827_hyb9829.CEL.gz 4.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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