"
Team:Kyoto/GoldenGateAssembly/Notebook
From 2012.igem.org
(→Golden Gate Assembly Notebook) |
(→Golden Gate Assembly Notebook) |
||
| Line 59: | Line 59: | ||
⑤PCR product of CFP | ⑤PCR product of CFP | ||
{|class="wikitable" | {|class="wikitable" | ||
| - | !10x Buffer KOD plus!!2mM dNTPs!!25mM MgSO4!!F primer!!R primer!!DNA( | + | !10x Buffer KOD plus!!2mM dNTPs!!25mM MgSO4!!F primer!!R primer!!DNA(①-⑤)!!KOD plus!!milliQ!!total |
|- | |- | ||
|2.5||2.5||1.0||0.75||0.75||0.5||0.5||16.5||25 | |2.5||2.5||1.0||0.75||0.75||0.5||0.5||16.5||25 | ||
|} | |} | ||
94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min20sec | 94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min20sec | ||
| + | |||
| + | ====PCR and Electrophoresis assay==== | ||
| + | ①DT | ||
| + | ②DT | ||
| + | ③CFP | ||
| + | ④CFP | ||
| + | {|class="wikitable" | ||
| + | !10x Buffer KOD plus!!2mM dNTPs!!25mM MgSO4!!F primer!!R primer!!DNA(①-④)!!KOD plus!!milliQ!!total | ||
| + | |- | ||
| + | |2.5||2.5||1.0||0.75||0.75||0.5||0.5||16.5||25 | ||
| + | |} | ||
| + | 94℃ 2min, (94℃ 15sec, 48℃ 30sec)x30cycles, 68℃ 1min | ||
</div> | </div> | ||
{{Kyoto/footer}} | {{Kyoto/footer}} | ||
Revision as of 08:22, 20 September 2012
Contents |
Golden Gate Assembly Notebook
August 10
Golden Gate Assembly method This method helps us to constract some genes quickly and we can design the order of constractions. We are trying to construct a gene cycle composed of 6 genes( pSB1A3, lacI, GFP, RFP, GFP, DT). After this experiment is confirmed to work, we will so some experiment to check how the numbers of promorters influences the strength of transcription.
September 6
PCR and Electrophoresis assay
①psB1K3 ②lacI ③GFP ④GFP ⑤RFP ⑥RFP ⑦CFP ⑧DT
| Quick Taq | primer F | primer R | DNA(①-⑧) | MilliQ | Total |
|---|---|---|---|---|---|
| 12.5 | 0.5 | 0.5 | 1 | 10.5 | 25 |
94℃ 2min, (94℃ 30sec, 50℃ 30sec)x25cycles, 68℃ 50sec
September 7
PCR and Electrophoresis assay
| 10x Buffer KOD plus | 2mM dNTPs | 25mM MgSO4 | F primer | R primer | DNA(psB1K3) | KOD plus | milliQ | total |
|---|---|---|---|---|---|---|---|---|
| 2.5 | 2.5 | 1.0 | 0.75 | 0.75 | 0.5 | 0.5 | 16.5 | 25 |
94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min
September 10
PCR and Electrophoresis assay
| 10x Buffer KOD plus | 2mM dNTPs | 25mM MgSO4 | F primer | R primer | DNA(CFP) | KOD plus | milliQ | total |
|---|---|---|---|---|---|---|---|---|
| 2.5 | 2.5 | 1.0 | 0.75 | 0.75 | 0.5 | 0.5 | 16.5 | 25 |
94℃ 2min, (94℃ 15sec, 48℃ 30sec)x30cycles, 68℃ 45sec
PCR and Electrophoresis assay
| 10x Buffer KOD plus | 2mM dNTPs | 25mM MgSO4 | F primer | R primer | DNA(lacI) | KOD plus | milliQ | total |
|---|---|---|---|---|---|---|---|---|
| 2.5 | 2.5 | 1.0 | 0.75 | 0.75 | 0.5 | 0.5 | 16.5 | 25 |
94℃ 2min, (94℃ 15sec, 51℃ 30sec)x30cycles, 68℃ 30sec
PCR and Electrophoresis assay
①PCR product of psB1K3 ②psB1K3 ③psB1C3 ④psB1K3 ⑤PCR product of CFP
| 10x Buffer KOD plus | 2mM dNTPs | 25mM MgSO4 | F primer | R primer | DNA(①-⑤) | KOD plus | milliQ | total |
|---|---|---|---|---|---|---|---|---|
| 2.5 | 2.5 | 1.0 | 0.75 | 0.75 | 0.5 | 0.5 | 16.5 | 25 |
94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min20sec
PCR and Electrophoresis assay
①DT ②DT ③CFP ④CFP
| 10x Buffer KOD plus | 2mM dNTPs | 25mM MgSO4 | F primer | R primer | DNA(①-④) | KOD plus | milliQ | total |
|---|---|---|---|---|---|---|---|---|
| 2.5 | 2.5 | 1.0 | 0.75 | 0.75 | 0.5 | 0.5 | 16.5 | 25 |
94℃ 2min, (94℃ 15sec, 48℃ 30sec)x30cycles, 68℃ 1min
