Difference between revisions of "YER186C"
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| + | ==UW Stout/FA 2022 Glycerol Media== | ||
| + | ===Introduction=== | ||
| + | Following the [[UW-Stout/Glycerol FA22]] protocol, 5 knockout strains of yeast cell were tortured within a glycerol media solution. | ||
| + | ===Results=== | ||
| + | ===Analysis/Conclusion=== | ||
Revision as of 13:29, 16 December 2022
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| Systematic name | YER186C |
| Gene name | |
| Aliases | |
| Feature type | ORF, Uncharacterized |
| Coordinates | Chr V:562625..561705 |
| Primary SGDID | S000000988 |
Description of YER186C: Putative protein of unknown function[1]
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Contents
Community Commentary
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DNA and RNA Details
Other DNA and RNA Details
Other Topic: expression
Specifically higher expression in phosphorus limited chemostat cultures versus phosphorus excess. [2] [3]
Caffeine
Interpretation
The average doubling time for the YEr186C (C3) gene in standard conditions was 87 minutes. Under caffeine stress, the average doubling time was 181 minutes. That is a 108% increase in doubling time which means that cell growth was negatively affected (slowed down) by this type of stress.
Ethanol
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References
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- ↑ SGD (2006) No information available SGD PMID
- ↑ Boer VM, et al. (2003) The genome-wide transcriptional responses of Saccharomyces cerevisiae grown on glucose in aerobic chemostat cultures limited for carbon, nitrogen, phosphorus, or sulfur. J Biol Chem 278(5):3265-74 SGD PMID 12414795
- ↑ submitted by Viktor Boer on 2003-07-25
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UW Stout/FA 2022 Glycerol Media
Introduction
Following the UW-Stout/Glycerol FA22 protocol, 5 knockout strains of yeast cell were tortured within a glycerol media solution.
