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Sample GSM1259803 Query DataSets for GSM1259803
Status Public on Mar 15, 2014
Title SAMPLE 6: GC ED
Sample type RNA
 
Source name Granulosa cell EarlyDom
Organism Equus caballus
Characteristics cell type: granulosa cell
developmental stage: EarlyDom
Extracted molecule total RNA
Extraction protocol Total RNA from granulosa and theca cells was extracted using TRIzol® according to manufacturer’s instructions (Life Technologies, Paisley, UK) and analysed using the Agilent Bioanalyzer 2100 (Agilent Technologies).
Label Cy3
Label protocol RNA of good quality (RIN>7.0) was reverse-transcribed (500 ng) with an oligo (dT) primer bearing a T7 promoter followed by cDNA purification and in vitro transcription with T7 polymerase to generate antisense RNA (aRNA) using the MessageAmp aRNA Kit (Life Technologies), as per manufacturer’s instructions. This was then purified, analysed on the Agilent Bioanalyzer 2100 and used to generate Cy3-labelled aRNA
 
Hybridization protocol Cy3-labelled aRNA was fragmented at 60C for 30 min and hybridised onto the Agilent Horse Gene Expression Microarray (version 2010; Agilent Technologies, Wokingham, UK) at 65C for 17 h using Agilent hybridisation chambers and oven.
Scan protocol Slides were washed and scanned with an Axon scanner (Molecular Devices LLC, Sunnyvale, CA, USA).
Description Gene expression in granulosa cells of early dominant follicles
Data processing The scanned images were analyzed with Feature Extraction Software 9.1 (Agilent) using default parameters to obtain background subtracted and spatially detrended Processed Signal intensities. Foreground log2(intensities) were normalized by quantile normalization .
 
Submission date Nov 05, 2013
Last update date Mar 15, 2014
Contact name Xavier Donadeu
E-mail(s) xavier.donadeu@roslin.ed.ac.uk
Organization name Roslin Institute, University of Edinburgh
Street address Easter Bush
City Midlothian
ZIP/Postal code EH25 9RG
Country United Kingdom
 
Platform ID GPL15189
Series (1)
GSE52109 Transcriptome profiling of dominant follicle development in the equine ovary

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
1 12.47997262
2 4.877402455
3 4.893509629
4 4.885205255
5 4.910591446
6 4.916151446
7 4.858230821
8 4.869968267
9 4.912268634
10 4.828599534
11 4.9424041
12 5.078089461
13 5.126945878
14 11.43601208
15 5.130848733
16 5.632993529
17 12.30912564
18 7.861501089
19 6.041776308
20 7.49421964

Total number of rows: 45220

Table truncated, full table size 779 Kbytes.




Supplementary file Size Download File type/resource
GSM1259803_25132210053_GE1-v5_95_Feb07_1_3.txt.gz 9.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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