Difference between revisions of "UW-Stout/Bud Scars FA22"

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Line 9: Line 9:
 
*Coverslip
 
*Coverslip
 
*Microscope
 
*Microscope
*Distilled Water ()
+
*Distilled Water (3,050 ul)
  
 
'''Procedure'''
 
'''Procedure'''

Revision as of 17:09, 20 December 2022


Materials

  • Wild type yeast culture
  • Knockout yeast culture
  • 1.7ml microcentrifuge tube (1 for each culture)
  • Calcofluor White Stain Kit Reagent B- Calcofluor White (1.0g), Evans Blue Dye (0.4g), and demineralized Water (1000.0ml) (10 ul for each culture)
  • Glass Microscope Slide
  • Coverslip
  • Microscope
  • Distilled Water (3,050 ul)

Procedure

  1. Gather materials
  2. Preserve cellular architecture and the composition of cells by adding 3.7% of formaldehyde and yeast cells to equal 1 ml of liquid
  3. Vortex briefly and let sit for 50 minutes
  4. Centrifuge (13k for 60 seconds) to make a pellet and remove liquid without disrupting the pellet
  5. Add 1 ml of water, vortex briefly, centrifuge (13k for 60 seconds), and remove liquid without disrupting the pellet
  6. Repeat steps 4 and 5
  7. Pellet, remove liquid and suspend in 10 ul of calcofluor
  8. Incubate at room temperature for 5 minutes
  9. Centrifuge (13k for 60 seconds) remove liquid
  10. Add 1 ml of water, vortex briefly, centrifuge (13k for 60 seconds), remove liquid
  11. Resuspend pellet in 50 ul of water
  12. Mount on the slide (5ul) and cover with a coverslip using petroleum jelly around the edges of the coverslip to prevent loss of moisture
  13. Put a paper towel below and above and cover with a heavy object for 10 minutes
  14. Look at the cells under a microscope and observe the number of bud scars on each cell. View 100 different cells