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Status |
Public on Aug 01, 2011 |
Title |
hybrid at rich media (YPD), 40min with Phenanthroline, Red dye, repeat #1 |
Sample type |
RNA |
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Source name |
S. cerevisiae BY4741 X S. paradoxus CBS432 (ho::kanMX4/ho::nat1 MATa/MATα)
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Organism |
Saccharomyces cerevisiae x Saccharomyces paradoxus |
Characteristics |
organism(s): hybrid growth protocol: YPD rich medium at 30°C, 40min with Phenanthroline
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Growth protocol |
S. cerevisiae, S. paradoxus and their hybrid were subjected to 150 ug/ml of 1,10-phenanthroline at log-phase and sampled after 0, 20, 40 and 60 minutes.
|
Extracted molecule |
polyA RNA |
Extraction protocol |
Total RNA was extracted using MasterPure™ Yeast RNA purification Kit (EPICENTRE).
|
Label |
Cy5
|
Label protocol |
Agilent Low RNA Input Amplificarion Kit (LRIAK) plus, two color.
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Hybridization protocol |
Agilent Gene Expression Hybridization Kit.
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Scan protocol |
Arrays were scanned using Agilent Microarray Scanner (p/n G2565BA) with a 5 micron resolution and photomultiplier tube (PMT) set to 100. The raw images were analyzed and quantified using Agilent Feature Extraction software.
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Data processing |
Raw hybridization intensities were processed by Agilent Feature Extraction software (default settings), log2-transformed, averaged over two replicate probes and corrected for %GC (the correction factor was defined by subtracting the avarage deviation of all probes with similar %GC from the avaerge of all probes).
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Submission date |
Apr 25, 2011 |
Last update date |
Aug 01, 2011 |
Contact name |
Itay Tirosh |
E-mail(s) |
itay.tirosh@weizmann.ac.il
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Organization name |
Weizmann Institute of Science
|
Department |
Molecular genetics
|
Lab |
Naama Barkai
|
Street address |
herzl
|
City |
Rehovot |
ZIP/Postal code |
76100 |
Country |
Israel |
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|
Platform ID |
GPL13449 |
Series (1) |
GSE28849 |
Coupled evolution of transcription and mRNA degradation. |
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