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Status |
Public on Nov 26, 2013 |
Title |
Transgenic yeast (pAG305GPD-AAE13) vs. control yeast (pAG305GPD-ccdB) |
Organism |
Saccharomyces cerevisiae |
Experiment type |
Expression profiling by array
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Summary |
The yeast expression vectors used to express AAE13 was constructed as follows: AAE13 (At3g16170) was amplified from the vector pENTR-AAE13. The amplified product was cloned into pCR®8⁄GW⁄TOPO® (Invitrogen). The resulting plasmid was combined with the Advanced Gateway destination vectors pAG305GPD-ccdB (Addgene, Boston, MA) in an attL X attR recombination reaction to generate the vectors pAG305GPD-AAE13. The integrating vector pAG305GPD-AAE13 was introduced into WAT11, which was also transformed empty vector pAG305GPD-ccdB as control (B1, B2, B3 and B4). The transgenic and control yeast cells were cultured in SD-drop out medium at 30 °C under shaken conditions, malonate was fed into cells at final concentration 0.2 mM when the value of OD600 reached at 0.1. The cells were harvested at mid-log phase.
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Overall design |
Two-condition experiment, Transgenic yeast (pAG305GPD-AAE13) vs. control yeast (pAG305GPD-ccdB). Biological replicates: 4 control replicates, 4 transgenic replicates.
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Contributor(s) |
Yu O, Wang Y |
Citation(s) |
24682482 |
Submission date |
Nov 25, 2013 |
Last update date |
May 18, 2017 |
Contact name |
Jinsheng Yu |
E-mail(s) |
jyu@wustl.edu
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Organization name |
Washington University School of Medicine
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Department |
Genetics
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Lab |
GTAC Lab
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Street address |
660 S. Euclid Ave.
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City |
St. Louis |
State/province |
MO |
ZIP/Postal code |
63110 |
Country |
USA |
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Platforms (1) |
GPL16244 |
Agilent-016322 Yeast (V2) Gene Expression 8x15K Microarray (Probe Name version) |
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Samples (4)
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GSM1274371 |
AAAE13_replicate_A1_ccdB_replicate_B1 |
GSM1274372 |
ccdB_replicate_B2 vs. AAAE13_replicate_A2 |
GSM1274373 |
AAAE13_replicate_A3_ccdB_replicate_B3 |
GSM1274374 |
ccdB_replicate_B4 vs. AAAE13_replicate_A4 |
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Relations |
BioProject |
PRJNA229864 |