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Sample GSM1820046 Query DataSets for GSM1820046
Status Public on Jul 03, 2017
Title Oenococcus oeni 3P2 [OoA1]
Sample type RNA
 
Source name Oenococcus oeni 3P2
Organism Oenococcus oeni
Characteristics strain: 3P2
Treatment protocol When cultures reached the late exponential phase (OD600nm ≈ 1) they were collected by centrifugation and inoculated in flasks of 500ml with wine like medium (2 g/L fructose, 2 g/L tartaric acid, 0.5 g/L citric acid, 0.6 g/L L-malic acid, 5 g/L yeast extract, 0.1 g/L acetic acid, 5 g/L glycerol and 12 % ethanol v/v, it was adjusted to a pH 3.4 with NaOH 1N)
Growth protocol O. oeni was cultured at 30ºC in MRS broth medium supplemented with L-malic acid (4 g l-1) and fructose (5 g l-1) at pH 5.0.
Extracted molecule total RNA
Extraction protocol Total RNA extractions were performed using the Roche RNeasy kit according to the manufacturer’s instructions (Mannheim, Germany).
Label Cy3
Label protocol dsDNA was generated from 10 mg RNA following Nimblegen array user's guide protocol. 1mg dsDNA was labeled by Klenow random priming with Cy3 nonamers with Nimblegen One-color DNA labeling kit (cat.# 06370411001) following manufacturer's user's guide
 
Hybridization protocol Cy3-labeled DNA was precipitated with 1 volume isopropanol. Hybridization mixture including 2mg labeled DNA was prepared using Nimblegen hybridization kit (cat.#05583683001). 090324_Ooen_exp Nimblegen arrays were hybridized in Nimblegen hybridization system 4 station for 16-18 h at 42ºC, and then washed in 1XWash solution I, II and III (cat.#5584507001).Hybridization buffers and washes were completed according to manufacturer's protocol
Scan protocol Arrays were scanned on a Genepix 4000B scanner
Description Oenococcus oeni total RNA from cells before inoculation in wine like medium (12% ethanol v/v)
Data processing Pair reports (raw data) listing the probe intensities of the arrays were extracted and processed using Nimblescan software v2.6
 
Submission date Jul 13, 2015
Last update date Jul 03, 2017
Contact name Cristina Reguant
E-mail(s) cristina.reguant@urv.cat
Phone +34 977558043
Organization name University Rovira i Virgili
Department Biochemistry and Biotechnology
Street address Marcel·lí Domingo 1
City Tarragona
State/province Tarragona
ZIP/Postal code 43007
Country Spain
 
Platform ID GPL19261
Series (1)
GSE70820 Transcriptomic analysis of three Oenococcus oeni strains in the early response to stress

Data table header descriptions
ID_REF
VALUE RMA normalized with NimbleGen software. Mean value of five analysis replicates has been log2 transformed.

Data table
ID_REF VALUE
OEOE_0001071000000001 9.91376
OEOE_0002071000000002 9.76148
OEOE_0003071000000003 11.4168
OEOE_0004071000000004 10.0079
OEOE_0005071000000005 12.3597
OEOE_0006071000000006 11.3588
OEOE_0007071000000007 6.0743
OEOE_0008071000000008 11.0891
OEOE_0009071000000009 11.0289
OEOE_0010071000000010 11.9541
OEOE_0011071000000011 13.3714
OEOE_0012071000000012 11.1978
OEOE_0013071000000013 11.873
OEOE_0014071000000014 8.13311
OEOE_0015071000000015 9.68418
OEOE_0017071000000016 8.96078
OEOE_0018071000000017 10.1688
OEOE_0019071000000018 9.09037
OEOE_0020071000000019 10.9845
OEOE_0021071000000020 10.3516

Total number of rows: 1611

Table truncated, full table size 47 Kbytes.




Supplementary file Size Download File type/resource
GSM1820046_415302_282_OoA1.pair.gz 1017.5 Kb (ftp)(http) PAIR
Processed data included within Sample table

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