NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2580057 Query DataSets for GSM2580057
Status Public on Jun 01, 2018
Title Venous blood_D95_P_W705
Sample type RNA
 
Source name Venous blood, 95 days, progressive, foal W705
Organism Equus caballus
Characteristics breed: Welsh Pony
tissue: whole blood
developmental stage: foal
gender: female
weening type: progressive
time after weaning: 95 days
horse id: W705
Treatment protocol 5ml venous blood were collected from the 32 foals, 30 and 95 days after weaning, using vacuum tubes which included a reagent that immediately stabilized intracellular RNA (PAXgene blood RNA system, PreAnalytiX GmbH, Hombrechtikon, Switzerland). The samples were kept at room temperature for 8 h as required for stabilizing RNA and then at -20°C until RNA extraction.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with the PAXgene Blood RNA kit (Qiagen, Courtaboeuf, France) according to the manufacturer's protocol. Total RNA quality was assessed and its concentration was measured using RNA Nano chips onto a Bioanalyser 2100 (Agilent, Boeblingen, Germany).
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 100 ng of DNase pre-treated (0.2μl DNase 10X, 0.4μl 10X Buffer DNase, 0.4μl RNasin 40U/μl, 3μl total RNA) total RNA using the One-Color Quick Amp Labeling kit (Agilent) according to the manufacturer's instructions, followed by RNA clean-up using Agencourt RNAClean XP (Agencourt Bioscience Corporation, Beverly, Massachusetts). Dye incorporation and cRNA yield were checked using Dropsense™ 96 UV/VIS droplet reader (Trinean, Belgium).
 
Hybridization protocol 600 ng of Cy3-labelled cRNA were hybridized on the microarray slides following the manufacturer’s instructions.
Scan protocol Immediately after washing, the slides were scanned on Agilent G2505C Microarray Scanner using Agilent Scan Control A.8.5.1 software.
Description Gene expression 95 days after progressive weaning in foal blood.
Data processing The fluorescence signal was extracted using Agilent Feature Extraction software v10.10.1.1 with default parameters.
Raw data (median of pixels intensity) were filtered, log2 transformed, corrected for batch effects (washing and labeling serials) and normalized using quantile method.
 
Submission date Apr 17, 2017
Last update date Feb 10, 2019
Contact name Aline FOURY
E-mail(s) aline.foury@inrae.fr
Organization name INRAE
Lab NutriNeuro
Street address 146 rue Léo Saignat
City Bordeaux
ZIP/Postal code 33600
Country France
 
Platform ID GPL23307
Series (2)
GSE97906 Effect of a progressive weaning on behavioural and physiologic indicators in foals (Equus caballus)
GSE97908 Effect of a progressive weaning on behavioural and physiologic indicators in foals and mares (Equus caballus)

Data table header descriptions
ID_REF
VALUE Normalized log2 signal intensity

Data table
ID_REF VALUE
5 22.73820285
6 24.96502921
8 29.60883698
9 35.03035096
11 25.67850634
12 15.14464198
13 31.07018024
16 37.51579174
17 33.45412964
18 16.12388543
19 31.62526132
20 43.03308646
21 32.36942703
22 31.81738105
23 49.51529397
25 18.1490117
27 40.09275196
29 13.11284991
30 27.57916227
32 29.56685242

Total number of rows: 26534

Table truncated, full table size 457 Kbytes.




Supplementary file Size Download File type/resource
GSM2580057_US10463851_258142110002_S01_GE1_1010_Sep10_2_4.txt.gz 11.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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