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Status |
Public on Jul 16, 2009 |
Title |
Pokkali root, control, biological replicate 1 |
Sample type |
RNA |
|
|
Source name |
root, Pokkali, control
|
Organism |
Oryza sativa Indica Group |
Characteristics |
salt-tolerant
|
Treatment protocol |
On day 22 after germination, salt treatment commenced by adding NaCl and CaCl2 (5:1 molar concentration) in two steps over a period of 3 days to the nutrient solution reservoir. Salinity in the treatment reservoir reached 7.4 dS/m. Plants were harvested on day 30.
|
Growth protocol |
Plants were grown in sand-filled tanks and irrigated with nutrient solution (for details see Walia et al (2005), Plant Physiol. 139:822-35) for 30 days.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted using TRIzol and subsequently purified using an RNeasy spin column (Qiagen) and an on-column DNase treatment.
|
Label |
biotin
|
Label protocol |
Approx. 8 µg of total RNA was processed to produce biotinylated cRNA targets.
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|
|
Hybridization protocol |
Standard Affymetrix procedures.
|
Scan protocol |
Standard Affymetrix procedures.
|
Description |
Pokkali control
|
Data processing |
The data were normalized using the Robust Multichip Average method of background correction, quantile normalisation, and summarisation of cell signal intensities (Irrizary et al., 2003).
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|
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Submission date |
Jan 13, 2009 |
Last update date |
Mar 11, 2009 |
Contact name |
Ute Baumann |
E-mail(s) |
[email protected]
|
Phone |
++61 8 83037388
|
Organization name |
University of Adelaide
|
Department |
Australian Centre for Plant Functional Genomics
|
Street address |
Hartley Grove
|
City |
Glen Osmond |
State/province |
SA |
ZIP/Postal code |
5064 |
Country |
Australia |
|
|
Platform ID |
GPL2025 |
Series (1) |
GSE14403 |
Root-specific transcriptional profiling of contrasting rice genotypes in response to salinity stress |
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