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Sample GSM2033184 Query DataSets for GSM2033184
Status Public on Jan 31, 2018
Title K1_Kan, biological rep 2, technical rep 2
Sample type RNA
 
Source name K1_Kan_2b
Organism Saccharomyces cerevisiae
Characteristics strain: K1_Kan
yeast type: wine
array: 1
block: 5
Growth protocol Haploid (mat alpha) flor yeast strain P3-D5 (indicated after P3_Kan as it carries a KanMx cassette) and haploid wine yeast K1-280-2B (mat a) were grown in a shaken liquid culture performed at 28°C, on a synthetic media mimicking wine. Cells were harvested at 1 O.D at 600nm. As the cells are shaken flor yeast do not produce a velum, nor wine strain that cannot produce any, so that in the end they grow in a similar maner.
Extracted molecule total RNA
Extraction protocol Total RNA extraction were perform with Trizol reagent (Gibco BRL, Life Technologies), purified by isopropanol precipitation then with RNeasy kit (Qiagen).
Label Cy3
Label protocol Cy3-labeled cRNA was synthesized with the One color RNA Spike-In kit (Agilent Technologies) and purified with RNeasy kit (Qiagen). Quality and quantity of RNA were controlled at each step by spectrometry (NanoDrop 1000, Thermo Scientific)
 
Hybridization protocol Agilent gene expression microarrays 8x15k was used for the micro array hybridization, with one-color method. Array design is based on ID 016322 (Agilent Technologies, Santa Clara, CA, USA). A quantity of 600ng of labeled cRNA were hybridized for 17h in 65°C in a rotative hybridization oven (Corning) using the Expression Hybridization kit (Agilent Technologies, 5188-5242). Plate were washed with expression wash buffer kit (Agilent Technologies, 5188-5325 5188-5326).
Scan protocol The array pictures were analyzed on a GenePix 4000B laser Scanner (Axon Instruments) and with the GenePix software Pro7
Description Gene expression in sample from K1_Kan strain, biological rep 2, technical rep 2
Data processing Data normalization and statistical analysis were performed using R 2.14.2 software and the limma package. Normalization was done by the quantile method considering all arrays
 
Submission date Jan 08, 2016
Last update date Jan 31, 2018
Contact name Jean-Luc Legras
E-mail(s) jean-luc.legras@inrae.fr
Organization name INRA
Department UMR1083, Science pour l'Oenologie
Lab Equipe Microbiologie - Physiologie Integrative
Street address 2, place Viala
City Montpellier cedex1
ZIP/Postal code 34060
Country France
 
Platform ID GPL16244
Series (1)
GSE76667 Domestication of flor yeast: Rewiring the map kinase signaling pathway for lifestyle switching

Data table header descriptions
ID_REF
VALUE Normalized log2 signal intensity

Data table
ID_REF VALUE
A_06_P1001 5.47296574
A_06_P1002 8.292429871
A_06_P1003 13.19381423
A_06_P1004 5.461168348
A_06_P1005 5.540630751
A_06_P1006 5.47296574
A_06_P1007 5.584405691
A_06_P1008 5.598198606
A_06_P1009 8.001854212
A_06_P1010 8.212340847
A_06_P1011 5.431576902
A_06_P1012 12.24277783
A_06_P1013 6.688870702
A_06_P1014 5.297485273
A_06_P1015 5.906890596
A_06_P1016 15.87756221
A_06_P1017 8.937259787
A_06_P1018 5.418723899
A_06_P1019 7.210164717
A_06_P1020 11.16111861

Total number of rows: 6227

Table truncated, full table size 139 Kbytes.




Supplementary file Size Download File type/resource
GSM2033184_251632210354_2013-10-03-560-560align_5-8.gpr.gz 1.5 Mb (ftp)(http) GPR
Processed data included within Sample table

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