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Team:Chiba/protocol/transformation
From 2008.igem.org
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Latest revision as of 03:34, 18 September 2008
Day 1 morning
- 100 ml SOB medium in 1L or 500 mL flask and sterilize
- E.coli culture grown in 2 mL of fresh LB medium.
Day 1 night
- Inoculate preculture (100 μL-1 mL) to sterile SOB medium.Shake culture vigoruoussly at 20-25 ℃ until OD is 0.4-0.6.
Day 2
- Transfer the culture to ice 10min.
- Prepare Wash buffer and Competent buffer by adding 3 mL Dilution buffer to 3 mL of Wash buffer(x2) and to 2.5 mL of Competent buffer(2x), respectively.(on ice)
- Pellet the cells by centrifugarion at 2500rpm for 6 min.
- Remove supernatant and genlly resupend the cells in 6 mL ice-cold Wash buffer(1x).
- Pellet the cells by centrifugarion at 2500rpm for 6 min.
- Completely remove the supernatant and gently resuspend the cells in 6 mL ice-cold Competent buffer(1x).
- Aliquot (on ice) 100μL of cell suspension into sterile 1.5 mL microtube and store in deep freezer.
