Team:KULeuven/13 August 2009
From 2009.igem.org
(Difference between revisions)
JochemDeen (Talk | contribs) |
Bart Bosmans (Talk | contribs) |
||
Line 1: | Line 1: | ||
{{Team:KULeuven/Common/BeginHeader}} | {{Team:KULeuven/Common/BeginHeader}} | ||
- | {{Team:KULeuven/Common/ | + | {{Team:KULeuven/Common/SubMenu_Notebook}} |
{{Team:KULeuven/Common/EndHeader}} | {{Team:KULeuven/Common/EndHeader}} | ||
{{Team:KULeuven/Notebook/DayNavigator}} | {{Team:KULeuven/Notebook/DayNavigator}} |
Revision as of 09:07, 4 September 2009
Project progress
Weekly meeting, presentation can be found here
Progress of parts
[edit] Blue Light Receptor
- PCR product of 12-august of pairt
- Miniprep of
Nanodrop results:
Part | concentration (ng/μl) | 260/280 λ | 260/230 λ |
---|---|---|---|
123,3 | 1,82 | ||
141,2 | 1,99 |
- Restriction digest cut with EcoRI and XbaI
- Electroporation of + and the ligation of ...
- Gelelectrophoresis of
- Only 1 band, so probably everything was cut
- Gelextraction of
- Nanodrop = 29,3 ng/μl
- Ligation of vector and insert
[edit] Vanillin Production
- Plated COMT (+RBS) from the registry
- Growing overnight in 37°C
- Plated ech
- From newly made liquid culture
- Miniprep of ech and sam8
- Nanodrop results:
Part | concentration (ng/μl) | 260/280 λ | 260/230 λ |
---|---|---|---|
ech | 72,7 | 1,94 | |
sam8 | 66,2 | 2,00 |
- Restriction digest on ech and sam8
- Gel electrophoresis on ech and sam8
- New electrocompetent cells were used for the electroporation with the old ligations
- Lig A -> sam5 + sam8
- Lig C -> ech + fcs
- Note: there was no spark
- Plating of the electroporated cells
- 200 μl per plate twice
- 600 μl left of A and C
[edit] Vanillin Receptor
- B and R miniprepped. Tomorrow proceed with mutagenesis of RpoA
- G redone (only TOPO was visible, 200bp) PCR from 2,3 and 1'
- W, X, Y, Z PCR purification to create a TOPO vector tomorrow
Nanodrop:
Part | concentration (ng/μl) | 260/280 λ | 260/230 λ |
---|---|---|---|
W | 46,1 | 1,84 | |
X | 112 | 1,82 | |
Y | 207 | 1,85 | |
Z | 155,3 | 1,86 |