|
Status |
Public on Oct 15, 2012 |
Title |
WT 0 mM NaCl, replicate 2 |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
WT 0 mM NaCl
|
Organism |
Oryza sativa |
Characteristics |
cultivar: Nipponbare genotype/variation: wild type age: day 3 tissue: 1 mm long root tip
|
Growth protocol |
Wild type and rss3 seedlings were grown on the MS medium in the absence or prescence of 100 mM NaCl for 3 days.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNAs were extracted from 1-mm root tips by RNeasy mini kit (Qiagen).
|
Label |
Cy5
|
Label protocol |
400 ng RNAs were labeled by Low RNA input Linear Amplification/Labeling Kit (Agilent).
|
|
|
Channel 2 |
Source name |
WT 0 mM NaCl (reference)
|
Organism |
Oryza sativa |
Characteristics |
cultivar: Nipponbarre genotype/variation: wild type age: day 3 tissue: 1 mm long root tip
|
Growth protocol |
Wild type and rss3 seedlings were grown on the MS medium in the absence or prescence of 100 mM NaCl for 3 days.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNAs were extracted from 1-mm root tips by RNeasy mini kit (Qiagen).
|
Label |
Cy3
|
Label protocol |
400 ng RNAs were labeled by Low RNA input Linear Amplification/Labeling Kit (Agilent).
|
|
|
|
Hybridization protocol |
Agilent protocol G4140-90050. 825 ng of each Cy-5- and Cy-3-labeled cRNAs were used for hybridization.
|
Scan protocol |
Using Agilent scanner model G2505B.
|
Data processing |
The scanned images were analyzed with Feature Extraction Software v10.5.1.1 (Agilent) to obtain background-subtracted and spatially-detrended Processed Signal intensities. All of the raw Cy-5 and Cy-3 signals (gBGSubSignal and rBGSubSignal, respectively) were normalized by variance stabilization normalization method using R software (http://www.r-project.org/). After normalization, the relative expression levels of genes were calculated by subtracting the Cy-5 values by Cy-3 values (reference). Relative log2 expressions were Z-scaled with R software.
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|
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Submission date |
Oct 10, 2012 |
Last update date |
Oct 18, 2012 |
Contact name |
yosuke toda |
E-mail(s) |
[email protected]
|
Organization name |
nagoya university
|
Street address |
furo-cho chikusa-ku
|
City |
nagoya |
State/province |
aichi-ken |
ZIP/Postal code |
464-8601 |
Country |
Japan |
|
|
Platform ID |
GPL6864 |
Series (1) |
GSE41442 |
Root tip: WT vs. rss3 and -NaCl vs. +NaCl |
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