Team:HokkaidoU Japan/Notebook/September23
From 2010.igem.org
- Amplifiable BAC plasmid ([http://partsregistry.org/Part:BBa_J61031 BBa_J61031]) purification
- Colony PCR of AraC+RBS+pSB1A3
- Electroporetion of BAC plasmid into DH5α MG1655
Bac Vecter Purification
Used Qiagen miniprep kit, qiaprep for miniprep
- Transfered 1.3 mL of BAC plasmid solution incubated overnight into 1.5 mL tube
- Centrifuged at 4C, 15000 rpm for 1 min
- Discarded the supernatant and added remaining solution.
- Centrifuged at 4C, 15000 rpm for 1 min
- Discarded the supernatant
- Suspended on 250 uL of Buffer P1
- Added 250 ul Buffer P2 inverted few times to mix, solution turned green
- Added 350 ul Buffer N3 mixed by inversion, precipitation apeared
- Centrifuged at 4C, 13000 rpm for 10 min
- Transfered the supernatant to filtration column
- Centrifuged at 4C, 13000 rpm for 1 min
- Discarded the flow-through
- added 500 uL of Buffer PB to filtration column
- Centrifuged at 4C, 13000 rpm for 1 min
- Discarded the flow-through centrifuged for 1min to remove remaining buffer
- Transfered filtration column to a new 1.5 ml tube
- Resuspended on 50 ul of TE and incubated at RT for 1min
- Centrifuged at 4C, 13000 rpm for 1 min
- Stored at -20C
Colony PCR of AraC+RBS+pSB1A3
- Selected 16 colonies at random, and PCRed them.
- PCR mix used is shown in the table bellow
Reagent | Amount |
---|---|
Taq Master Mix | 80 uL |
Ex-F | 1.6 uL |
Ps-R | 1.6 uL |
Total | 83.2 uL |
- electrophoresed the samples
1 lane -> Marker λ/HindIII EcoRI 5 uL
2~8 lane -> colony No.1~7
9 lane -> Marker λ/HindIII EcoRI 5 uL
10~16 lane -> colony No.8~14
Colony No.15,16 didn't electrophorese.
- Colony No.1 will have the plasmid,so we put the sample into 2 mL LB added 2 uL Ampicillin(100 ug/uL).Incubated it in a shaker at 37C, 180 rpm.