Team:HokkaidoU Japan/Notebook/September30
From 2010.igem.org
- Digestion and Ligation of Arabinose Promoter,T3SSsignal and pSB1T3
- Transformation
parts information
Arabinose Promoter 1210bp(+primer:1259bp)
3-20B pSB2K3
PCRed in 21 September
RBS+T3SSsignal 583bp(+primer:636bp)
PCRed in 29 September
pSB1T3 2463bp(+primer:2504bp)
PCRed in 26 August
Digestion and Ligation of Arabinose Promoter,T3SSsignal and pSB1T3
1.digestion mix was made according to the table below
Reagent | Amount |
---|---|
10x H buffer | 2 uL |
DW | 1.6 |
pSB1T3 | 1 |
BSA | 2 |
EcoR I | 0.2 |
Pst I | 0.2 |
Total | 20 uL |
Reagent | Amount |
---|---|
10x H buffer | 2 uL |
DW | 11.7 |
Promoter | 3.5 |
BSA | 2 |
EcoR I | 0.5 |
Spe I | 0.3 |
Total | 20 uL |
Reagent | Amount |
---|---|
10x M buffer | 5 uL |
DW | 32.8 |
T3SSsignal | 2.5 |
BSA | 5 |
Xba I | 4.5 |
Pst I | 0.2 |
Total | 50 uL |
2.incubated at 37C for an hour
3.electrophoresed 3 samples with 6uL λ/HindⅢ EcoRI
写真:9/30 14:01
4.extracted 3 samples from a gel
5.added 4.5 ul 3M CH3COONa
6.added 125 uL 100% EtOH
7.centrifuged at 4C,15000rpm for 5min
8.discarded the supertenant
9.added 100 uL 70% EtOH
10.centrifuged at 4C,15000rpm for 5min
11.dry up the samples
12.dissolved the samples with 2 uL TE
13.mixed the 3 samples
14.added 6 uL Mighty Mix
15.incubated at 16C for 30 min
16.put the sample into 100 uL competent cell
17.incubated at 0C for 30 min
18.heatshocked at 42C for 60 sec
19.incubated at 0C for 5min
20.added 400 uL SOB
21.incubated at 30C for an hour and a half
22.incubated at 37C for 45min
23.