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Team:KULeuven/20 August 2009
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| - | + | Weekly meeting today, presentation can be found [https://2009.igem.org/Image:Presentatie_20-08.pdf here] | |
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Latest revision as of 08:48, 10 September 2009
Project progress
Weekly meeting today, presentation can be found here
Progress of parts
[edit] Blue Light Receptor
[edit] Vanillin Production
1)
- EF colonies present! So, we took 1ml off for further growth and miniprepped the remaining 4ml in triple
- Nanodrop concentrations:
| Part | concentration (ng/μl) | 260/280 λ | |
|---|---|---|---|
| EF A | 74,9 | 1,89 | |
| EF B | 63,1 | 1,87 | |
| EF C | 53,9 | 1,90 |
- We performed a digest with EcoRI and SpeI to cut out the insert and check it's length. Enzymes were added separately, with 1h in between. Total volume was 30µl.
- Calculations restriction
| Part | µl DNA | µl MQ | |
|---|---|---|---|
| EF C | 9,3 | 20,7 |
- In the afternoon, the remaining 1ml was re-plated and put on 37°C
2)
- Test 1: Results from yesterday's restriction test were inconclusive, because the DNA ladder didn't run properly so the length of the fragments couldn't be read. Therefore, we did it again...
- Restriction=OK! Test 1 completed.
3)
- Test 2: cutting with 2 enzymes subsequently (1h incubation in between) in a volume of 30µl. Using a larger volume should dilute the glycerol, which inhibits cutting. After that, the products are incubated overnight to allow full restriction. sam8 and fcs are cut with EcoRI and SpeI; sam5 and ech are cut with EcoRI and XbaI
- Calculations restriction
| Part | µl DNA | µl MQ | |
|---|---|---|---|
| Sam8 B | 7,9 | 22,1 | |
| Sam5 B | 4,0 | 26,0 | |
| Ech B | 5,2 | 24,8 | |
| Fcs B | 4,4 | 25,6 |
[edit] Vanillin Receptor
- Restriction digest of X, Y and with EcoR1 and Pst1
- Gelelectrophoresis to check fragments and gelextraction
- Fluid medium from outplated cells (overgrowth)
- TOPO-cloning (with new protocol from Invitrogen) for W and Z
