UW-Stout/Bud Scars FA22

From SGD-Wiki
Revision as of 12:20, 15 December 2022 by Teagueb (talk | contribs) (Created page with " '''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....")
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to: navigation, search


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 ()

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 pellet
  5. Add 1 ml of water, vortex briefly, centrifuge (13k for 60 seconds), remove liquid without disrupting 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 slide (5ul) and cover with 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 amount of bud scars on each cell. View 100 different cells