Team:HokkaidoU Japan/Notebook/August30
From 2010.igem.org
(Difference between revisions)
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|style="border-top:1px solid #996;"|20 uL | |style="border-top:1px solid #996;"|20 uL | ||
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- | [[Image:HokkaidoU Japan 20100830a.jpg|200px|right|thumb|]] | + | [[Image:HokkaidoU Japan 20100830a.jpg|200px|right|thumb|Electrophoresis of digestion products]] |
- | + | →Incubated at 37C for 60 min | |
- | === | + | ===Electrophoresis=== |
- | * | + | * Markers used [https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png Lambda/''Hin''dIII, EcoR I] and 50bp ladder |
- | + | * Was obvious that parts were cut as intended | |
- | * | + |
Revision as of 17:05, 27 September 2010
Digestion of pUC119 by EcoR I, Pst I
- | EcoR I | Pst I | E, P | 古いEcoR I | |
DNA solution | 1 uL | 1 uL | 1 uL | 1 uL | 1 uL |
DW | 17 uL | 14 uL | 14 uL | 13 uL | 14 uL |
10x M buffer | 2 uL | 2 uL | 2 uL | 2 uL | 2 uL |
0.1% BSA | - | 2 uL | 2 uL | 2 uL | 2 uL |
EcoR I | - | 1 uL | - | 1 uL | 1 uL |
Pst I | - | - | 1 uL | 1 uL | - |
Total | 20 uL | 20 uL | 20 uL | 20 uL | 20 uL |
→Incubated at 37C for 60 min →Electrophoresed 2 uL for confirmation
- There were no bands, forgot to add DNA :(
- Reused the remaining 18 uL of digestion solution by adding 1 uL of ADW and 1uL of DNA
→Incubated at 37C for 60 min
→Electrophoresed 2 uL of each solution(+ 0.4 uL 6x SB)
Electrophoresis
Lane | DNA |
2 | Lambda/HindIII, EcoR I(4 uL used) |
3 | Undigested |
4 | EcoR I |
5 | Pst I |
6 | EcoR I + Pst I |
7 | EcoR I (used old enzyme to check it's activity) |
- In lane 3 monomers, dimers and trimers of plasmid were visible .
- From lanes 4 through 7 it's visible that DNA digestion wasn't satisfactory
- Because plasmid became linear it's was slower than super-coiled one's
Digestion of parts PCRed using digestion visualization primers
RBS | dT | GFP | ||||||||||
DNA | 1 uL | 1 uL | 1 uL | 1 uL | 1 uL | 1 uL | 1 uL | 1 uL | 1 uL | 1 uL | 1 uL | 1 uL |
DW | 17 uL | 14 uL | 14 uL | 13 uL | 17 uL | 14 uL | 14 uL | 13 uL | 17 uL | 14 uL | 14 uL | 13 uL |
10x M buffer | 2 uL | 2 uL | 2 uL | 2 uL | 2 uL | 2 uL | 2 uL | 2 uL | 2 uL | 2 uL | 2 uL | 2 uL |
0.1% BSA | - | 2 uL | 2 uL | 2 uL | - | 2 uL | 2 uL | 2 uL | - | 2 uL | 2 uL | 2 uL |
EcoR I | - | 1 uL | - | 1 uL | - | 1 uL | - | 1 uL | - | 1 uL | - | 1 uL |
Pst I | - | - | 1 uL | 1 uL | - | - | 1 uL | 1 uL | - | - | 1 uL | 1 uL |
Total | 20 uL | 20 uL | 20 uL | 20 uL | 20 uL | 20 uL | 20 uL | 20 uL | 20 uL | 20 uL | 20 uL | 20 uL |
→Incubated at 37C for 60 min
Electrophoresis
- Markers used Lambda/HindIII, EcoR I and 50bp ladder
- Was obvious that parts were cut as intended