20.109(S14): TA notes for module 2: Difference between revisions
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Suhani Vora (talk | contribs) (→Day 2) |
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'''Materials required:''' | '''Materials required:''' | ||
Please read as much as you can of Parts 1-3 and create an automated worksheet (e.g., in Excel) that will perform the required calculations for the day. A partially prepared worksheet is [[Media: S14_M2D2-starter.xlsx | '''linked here''']]. We will NOT collect your final worksheet this time; it is only for your benefit. | Please read as much as you can of Parts 1-3 and create an automated worksheet (e.g., in Excel) that will perform the required calculations for the day. A partially prepared worksheet is [[Media: S14_M2D2-starter.xlsx | '''linked here''']]. We will NOT collect your final worksheet this time; it is only for your benefit. | ||
Prep. For westerns: | |||
Make aliquots: | |||
Chill scrapers | |||
RIPA lysis buffer | |||
Protease inhibitor (last minute) | |||
Eppendorf tubes | |||
PBS for wash | |||
Ice buckets | |||
Set up boiling station: | |||
Turn on hot plates with water in glass bowl with boiling chips | |||
Aliquot beta-mercap. | |||
Don't forget to show students the cap covers | |||
Set up westerns: | |||
Make sds running buffer | |||
Make transfer buffer (chilled) | |||
Set up gels(remove strips, place in boxes, remove combs, wash wells with running buffer) | |||
Night before: freeze ice blocks | |||
Presoak filter paper and scotch pads in transfer buffer for 30 min prior to blot. | |||
Make sure we have blocking buffer. | |||
'''Day of Lab (R/F):''' | '''Day of Lab (R/F):''' |
Revision as of 14:02, 22 March 2014
General notes
I need to figure out the quiz dates.
See also GoogleDoc for aliquoting amounts.
Scheme: Each pair of students will test K1 and xrs6 cells for Ku80 production. They will then assess the ability of K1, xrs6, and DNA-PKcs inhibited cells to repair DNA damage via plasmid based assay and flow cytometry.
Key preparation:
Cells:
- Prepare T25 flasks of K1 and xrs6 for every team
Westerns:
- Prepare transfer buffer
DNA plasmids:
- Aliquot plasmids
Lipofection: Flow cytometry:
Note to TA:
- While you read the wiki, test each link, and make any link descriptions bold that are not already.
- As you read the protocols, add reagent calculations to the GoogleDoc as needed.
Day-by-day
Day 1
Materials required:
1. Aliquots of PBS, CHO media, and 0.25% Phenol Red Trypsin for each group 2. T25 flask of K1 and xrs6 cells for each group
- Flasks for next day seeded at 600,000 cells
- Flasks for day after next, seeded at 400,000 cells
- Flasks for 3 days in future, seeded at 200,000 cells
Day of Lab (T/W):
- No Quiz
- Prepare remaining aliquots for students
- Warm up media, PBS, and trypsin half hour before students use reagents
Additional Prep.:
- Digest pMAX-BFP-2MCS2 for testing damage topologies
- Pour gel for purification
After Lab:
- Aliquot new shipment of trypsin
How it went:
Day went pretty smoothly; not many questions on Part 4 exercise.
Day 2
Materials required: Please read as much as you can of Parts 1-3 and create an automated worksheet (e.g., in Excel) that will perform the required calculations for the day. A partially prepared worksheet is linked here. We will NOT collect your final worksheet this time; it is only for your benefit.
Prep. For westerns: Make aliquots: Chill scrapers RIPA lysis buffer Protease inhibitor (last minute) Eppendorf tubes PBS for wash Ice buckets
Set up boiling station: Turn on hot plates with water in glass bowl with boiling chips Aliquot beta-mercap. Don't forget to show students the cap covers
Set up westerns: Make sds running buffer Make transfer buffer (chilled) Set up gels(remove strips, place in boxes, remove combs, wash wells with running buffer) Night before: freeze ice blocks
Presoak filter paper and scotch pads in transfer buffer for 30 min prior to blot.
Make sure we have blocking buffer.
Day of Lab (R/F):
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Day 3
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Day 4
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Day 5
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Day 6
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Day 7
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Day 8
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