Difference between revisions of "UW-Stout/Hydroxychloroquine SP21"

From SGD-Wiki
Jump to: navigation, search
(Materials)
(Equipment)
Line 7: Line 7:
 
==Equipment==
 
==Equipment==
 
* [https://www.moleculardevices.com/sites/default/files/en/assets/data-sheets/br/spectramax-plus-384-microplate-reader.pdf Molecular Devices SpectraMax Plus 384 Microplate Reader]
 
* [https://www.moleculardevices.com/sites/default/files/en/assets/data-sheets/br/spectramax-plus-384-microplate-reader.pdf Molecular Devices SpectraMax Plus 384 Microplate Reader]
 +
==Precautions==
 +
Use gloves and safety glasses for this experiment. Hydroxychloroquine is a potent chemical used to treat malaria and some autoimmune conditions. However, side effects include but are not limited to nausea, headache, dizziness, rash.
  
 
==Calibration Protocol==
 
==Calibration Protocol==

Revision as of 09:43, 27 April 2021

Materials

Equipment

Precautions

Use gloves and safety glasses for this experiment. Hydroxychloroquine is a potent chemical used to treat malaria and some autoimmune conditions. However, side effects include but are not limited to nausea, headache, dizziness, rash.

Calibration Protocol

  1. This experiment is designed to test the growth response of wild strain yeast cells to various concentrations of hydroxychloroquine, a lysosome disruptor. This is done to find out the most suitable concentration of the torture factor to exert stress on the cells, but not destroy them.

Precautions

Use gloves and safety glasses for this experiment. Hydroxychloroquine is a potent chemical used to treat malaria and some autoimmune conditions. However, side effects include but are not limited to nausea, headache, dizziness, rash.

Materials

Protocol

  1. Vortex the yeast culture briefly to resuspend the yeast cells.
  2. Set up seven wells aliquoting 50uL of the stock hydroxychloroquine and 50uL of yeast culture. Use the seventh well for the wild-type yeast strain.
    • The final concentration of hydroxychloroquine is 300ug/mL.
  3. To measure cell growth over a period of 24 hours, set up the plate reader as follows:
    • Temperature: 30°C
    • Mode: Kinetic
    • Wavelength: 600 nm
    • Interval: 5 minutes
    • Total run time: 24 hours
    • Shake before reading: 30 seconds
  4. Transfer the assay plate to the reader and read for 24 hours.
    • Note: Repeat the experiment a few times to account for natural variation.