Difference between revisions of "UW-Stout/Ultraviolet Light"
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# The morning of the experiment, dilute each culture to an OD600 of 0.2 in YPD broth. Return to the drum roller for between 30 and 90 minutes. | # The morning of the experiment, dilute each culture to an OD600 of 0.2 in YPD broth. Return to the drum roller for between 30 and 90 minutes. | ||
# Transfer 33 µl to a well in the assay plate. | # Transfer 33 µl to a well in the assay plate. | ||
| − | # Set up the UV light as follows: | + | # Set up the UV light Exposeure System as follows: |
#*400 watts | #*400 watts | ||
#*time increments | #*time increments | ||
Revision as of 08:00, 30 April 2019
Contents
Materials
- YPD media, both broth and 2% agar plates]
- Glycerol stocks of knockout strains
- [1]
Equipment
- Incubator set to 30°C.
- Bachur & Associates Sanata Clara, CA 95050 Model LS-100-3 UV Light Exposeure System
Protocol
- Three days before the experiment, streak knockout strains onto YPD plates.
- One day before the experiment, pick a colony from each strain into 5 ml YPD broth in a disposable test-tube. Incubate on the roller drum at 30°C overnight.
- The morning of the experiment, dilute each culture to an OD600 of 0.2 in YPD broth. Return to the drum roller for between 30 and 90 minutes.
- Transfer 33 µl to a well in the assay plate.
- Set up the UV light Exposeure System as follows:
- 400 watts
- time increments
- place in the incubator in dark for 48 hours
