Difference between revisions of "UW-Stout/G418 FA21"
(→KO Gene Protocol) |
(→KO Gene Protocol) |
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Line 254: | Line 254: | ||
Well 2: | Well 2: | ||
− | -50 ul | + | -50 ul YHL012W gene |
-50 ul 0.0456mg/ml G418 | -50 ul 0.0456mg/ml G418 | ||
Line 261: | Line 261: | ||
Well 3: | Well 3: | ||
− | -50 ul | + | -50 ul YMR221C gene |
-50 ul 0.0456mg/ml G418 | -50 ul 0.0456mg/ml G418 | ||
Line 268: | Line 268: | ||
Well 4: | Well 4: | ||
− | -50 ul | + | -50 ul YPR078C gene |
-50 ul 0.0456mg/ml G418 | -50 ul 0.0456mg/ml G418 | ||
Line 275: | Line 275: | ||
Well 5: | Well 5: | ||
− | -50 ul | + | -50 ul YBR184W gene |
-50 ul 0.0456mg/ml G418 | -50 ul 0.0456mg/ml G418 | ||
Line 282: | Line 282: | ||
Well 6: | Well 6: | ||
− | -50 ul | + | -50 ul YBR284W gene |
-50 ul 0.0456mg/ml G418 | -50 ul 0.0456mg/ml G418 | ||
Line 296: | Line 296: | ||
Well 8: | Well 8: | ||
− | -50 ul | + | -50 ul YHL012W gene |
-50 ul 0.0456mg/ml G418 | -50 ul 0.0456mg/ml G418 | ||
Line 303: | Line 303: | ||
Well 9: | Well 9: | ||
− | -50 ul | + | -50 ul YMR221C gene |
-50 ul 0.0456mg/ml G418 | -50 ul 0.0456mg/ml G418 | ||
Line 310: | Line 310: | ||
Well 10: | Well 10: | ||
− | -50 ul | + | -50 ul YPR078C gene |
-50 ul 0.0456mg/ml G418 | -50 ul 0.0456mg/ml G418 | ||
Line 317: | Line 317: | ||
Well 11: | Well 11: | ||
− | -50 ul | + | -50 ul YBR184W gene |
-50 ul 0.0456mg/ml G418 | -50 ul 0.0456mg/ml G418 | ||
Line 324: | Line 324: | ||
Well 12: | Well 12: | ||
− | -50 ul | + | -50 ul YBR284W gene |
-50 ul 0.0456mg/ml G418 | -50 ul 0.0456mg/ml G418 |
Revision as of 13:32, 20 December 2021
Calibration Protocol
Materials
Safety Gloves
Safety Glasses
Well Plate
Molecular Devices SpectraMax Plus 384 Microplate Reader
Fume Hood
Sterile Water
G418
Pipettes
Wild Type Yeast
5 Knockout Yeast
Protocol
1. Obtain 10 different concentrations of the G418 antibiotic and sterile water. Make sure to have 1 extra concentration of sterile water as a control growth curve of the wild type yeast.
2. Set up 11 wells shown in the "Well Components".
3. Put the well plate to the reader and read for 24 hours.
4. Observe the the growth curves.
5. Determine which concentration should be used on the knockout yeast.
Concentrations Used
1. 100mg/ml G418
- 200ul G418
-0ul water
2. 33.3mg/ml G418
-66.7ul G418
-133.3ul water
3. 11.1mg/ml G418
-22.2ul G418
-177.8ul water
4. 3.7mg/ml G418
-7.4ul G418
-192.6ul water
5. 1.23mg/ml G418
-2.5ul G418
-197.5ul water
6. 0.41mg/ml G418
-1.6ul G418
-398.4ul G418
7. 0.41mg/ml G418
-1.1ul G418
-800ul water
8. 0.0456mg/ml G418
-1.4ul G418
-3,000ul water
9. 0.0152mg/ml G418
-1.5ul G418
-10,000ul water
10. 0.0050mg/ml G418
-1.0ul G418
-20,000ul water
11. 0mg/ml G418 (control)
-0ul G418
-200ul water
Note: For concentrations 6-10, serial dilutions were made. This is because the amount of G418 used would have been to small to physically preform.
Well Components
Well 1:
-50 ul wt yeast
-50 ul 100mg/ml G418
Well 2:
-50 ul wt yeast
-50 ul 33.3mg/ml G418
Well 3:
-50 ul wt yeast
-50 ul 11.1mg/ml G418
Well 4:
-50 ul wt yeast
-50 ul 3.7mg/ml G418
Well 5:
-50 ul wt yeast
-50 ul 1.23mg/ml G418
Well 6:
-50 ul wt yeast
-50 ul 0.41mg/ml G418
Well 7:
-50 ul wt yeast
-50 ul 0.137mg/ml G418
Well 8:
-50 ul wt yeast
-50 ul 0.0456mg/ml G418
Well 9:
-50 ul wt yeast
-50 ul 0.0152mg/ml G418
Well 10:
-50 ul wt yeast
-50 ul 0.0050mg/ml G418
Well 11:
-50 ul wt yeast
-50 ul water
Data
Based on the data from the Molecular Devices SpectraMax Plus 384 Microplate Reader, we decided to use the concentration from well 8 (E8).
KO Gene Protocol
Materials
Safety Gloves
Safety Glasses
Well Plate
Molecular Devices SpectraMax Plus 384 Microplate Reader
Fume Hood
Sterile Water
G418
Pipettes
Wild Type Yeast
5 Knockout Yeast
Protocol
1. Obtain the concentration determined from the calibration protocol (0.0456mg/ml G418).
2. Set up 12 wells as described in "Well Components".
3. In the well plates there will be 2 of the same components. (There are 5 KO yeasts and 1 wild type)
4. Put the well plate to the reader and read for 24 hours.
5. Observe the the growth curves.
Well Components
Well 1:
-50 ul wt yeast
-50 ul 0.0456mg/ml G418
Well 2:
-50 ul YHL012W gene
-50 ul 0.0456mg/ml G418
Well 3:
-50 ul YMR221C gene
-50 ul 0.0456mg/ml G418
Well 4:
-50 ul YPR078C gene
-50 ul 0.0456mg/ml G418
Well 5:
-50 ul YBR184W gene
-50 ul 0.0456mg/ml G418
Well 6:
-50 ul YBR284W gene
-50 ul 0.0456mg/ml G418
Well 7:
-50 ul wt yeast
-50 ul 0.0456mg/ml G418
Well 8:
-50 ul YHL012W gene
-50 ul 0.0456mg/ml G418
Well 9:
-50 ul YMR221C gene
-50 ul 0.0456mg/ml G418
Well 10:
-50 ul YPR078C gene
-50 ul 0.0456mg/ml G418
Well 11:
-50 ul YBR184W gene
-50 ul 0.0456mg/ml G418
Well 12:
-50 ul YBR284W gene
-50 ul 0.0456mg/ml G418
Data
Analysis of our data through doubling rates: