Team:Stockholm/Protocols
From 2010.igem.org
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# Put metal blocks in -80 degree C. | # Put metal blocks in -80 degree C. | ||
# Snapfreeze 100 mikroL aliquots in ice-cold Epps (in pre-chilled blocks). Store in -80 degree C freezer. | # Snapfreeze 100 mikroL aliquots in ice-cold Epps (in pre-chilled blocks). Store in -80 degree C freezer. | ||
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==Competent cells (Andreas & Mimmi)== | ==Competent cells (Andreas & Mimmi)== |
Revision as of 09:35, 6 July 2010
Contents |
Competent cells (Nina & Johan)
From Morten Nørholm at the Department of Biochemistry & Biophysics Stockholm University
- Add 5 ml LB in two 50 ml falcon tubes. Add the top of a tip bacteria into the two 5 ml LB. Grow ON in shake incubator 37 degree C.
- Subculture each 5 ml of starterculture into two 400 ml pre-warmed LB. Grow at 37 degree C until OD reaches 0.6.
- Put cells on ice for 20 min.
- Harvest cells at 4000 rpm for 20 min, 4 degree C.
- Discard supernatant if it looks clear (or spinn longer if it is cloudy).
- Resuspend pellet carefully in 500 50 mM CaCl2 for a 1000 ml cell culture (1/2 the orifinal volume).
- Put cells on ice 20 min.
- Repeat step 5.
- Resuspend cells in 16 ml CaCl2 + 15% Glycerol for a 800 ml starter culture (1:50 volume)
- Put metal blocks in -80 degree C.
- Snapfreeze 100 mikroL aliquots in ice-cold Epps (in pre-chilled blocks). Store in -80 degree C freezer.
Competent cells (Andreas & Mimmi)
Based and modified from the Top10 protocol by the Knight lab
Materials
CCMB80 buffer
- 10 mM KOAc pH 7.0
- 80 mM CaCl2.2H2O
- 20 mM MnCl2
- 10 mM MgCl2.6H2O
- 10% glycerol
Procedures
- Set an ON starter culture by inoculating 5 ml LB and incubating ON in 37°C with 250 rpm rotary shaking.
- Inoculate 250 ml new LB with 2 ml from the ON culture and grow in 30°C, 250 rpm until an OD(600) of ≈0.3.
- Use a large, 1 l E-flask.
- Spin down cells at 3000 x g for 10 min in 4°C.
- Remove supernatant and resuspend cells in 80 ml ice-cold CCMB80 buffer. Keep cells on ice for 20 min.
- Spin down cells again with same settings. Resuspend in 10 ml new CCMB80 buffer and keep on ice for 20 min.
- Aliquot 100 ul samples of competent cells into 1.5 ml vials and store in -80°C, or transform immediately.
Transformation (Andreas & Mimmi)
- Add 1 ul plasmid to 100 ul thawed, competent cells of choice. Hold cells on ice for 30 min.
- Heat-shock cells for 55 sec in 42°C. Return to ice.
- Add 900 ul LB medium and grow cells in 37°C, 250 rpm for 1 hour.
- This allows cells to start expressing antibiotic resistance gene(s).
- Spin down cells at full speed (≈13.000 x g) for 15 sec.
- Remove 900 ul from the supernatant and gently resuspend pellet in remaining 100 ul.
- Plate 100 ul cells onto an LB agar plate with appropriate antibiotic(s).