IGEM:Melbourne/2008/Protocols/competent cells: Difference between revisions
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==Procedure== | ==Procedure== | ||
1) Grow 130ml LB culture from the 5ml grew previously to | 1) Grow 130ml LB culture from the 5ml grew previously to OD600 of NO MORE than 0.45 | ||
2) Pour cultures into sterile 50ml falcon tubes | |||
3) Pellet cells at 4 degree, 3000rpm for 5 min | |||
4) Discard supernatant | |||
5) Resuspend pellet in total volume of 50ml ice-cold TFB1 | |||
6) Chill on ice for 5 min | |||
7) Pellet cells at 4 degree, 3000rpm for 5 min | |||
8) Discard supernatant | |||
9) Resuspend pellet in 5 ml of ice-cold TFB2 | |||
10) Chill on ice for 15 min | |||
11) Aliquot on dry ice, then snap-freeze, then store at -80 degree | |||
Latest revision as of 16:16, 21 April 2008
- yield 5ml ~ 100 aliquots of 50µL
- need another overnight culture (5ml)
Procedure
1) Grow 130ml LB culture from the 5ml grew previously to OD600 of NO MORE than 0.45
2) Pour cultures into sterile 50ml falcon tubes
3) Pellet cells at 4 degree, 3000rpm for 5 min
4) Discard supernatant
5) Resuspend pellet in total volume of 50ml ice-cold TFB1
6) Chill on ice for 5 min
7) Pellet cells at 4 degree, 3000rpm for 5 min
8) Discard supernatant
9) Resuspend pellet in 5 ml of ice-cold TFB2
10) Chill on ice for 15 min
11) Aliquot on dry ice, then snap-freeze, then store at -80 degree
