Team:Chiba/Notebook/Calendar/18 September 2009
From 2009.igem.org
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- | (4):2 + | + | (4):2 + 4 ---LuxI/LasI-GFP |
- | (5):2 + | + | (5):2 + 3 ---LuxI/LuxR-GFP |
- | (6):2 + 5 | + | (6):2 + 5 ---LuxI/LuxR-RFP |
- | (7): | + | (7):4 + flesh LB ---LasR-GFP |
- | (8): | + | (8):3 + flesh LB ---LuxR-GFP |
- | (9):5 + flesh LB | + | (9):5 + flesh LB ---LuxR-RFP |
== Lab Notebook == | == Lab Notebook == | ||
[[Image:Chiba-Labwork-17Sep09.jpg|200px]] [[Image:Chiba-Labwork-18Sep09.jpg|200px]] | [[Image:Chiba-Labwork-17Sep09.jpg|200px]] [[Image:Chiba-Labwork-18Sep09.jpg|200px]] | ||
[[Image:Chiba-Labwork-17Sep09-5.jpg|200px]] [[Image:Chiba-Labwork-17Sep09-2.jpg|200px]] | [[Image:Chiba-Labwork-17Sep09-5.jpg|200px]] [[Image:Chiba-Labwork-17Sep09-2.jpg|200px]] |
Revision as of 06:48, 23 September 2009
(17_September_2009 <|>19_September_2009)
LuxR Mutants Sequence
Purification of DNA
- isopropanol precipitation and analysis
- add isopropanol(75%) 50 uL to PCR solution made yesterday
- VORTEX and centrifugation(14000 rpm 10 min)
- put off the supernatant fluid
- add isopropanol(75%) 50 uL
- centrifugation(14000 rpm 10 min)
- put off the supernatant fluid
- drying 60 degrees C 15min
- add ddH2O 20 uL and VORTEX
- sequence analysis
Las Check
Culture Mix
- K084007:LasI
- K084012:LuxI
- T9002:LuxR-GFP
- K091134:LasR-GFP
- I731012:LuxR-RFP
Sender:Receiver=0.8 mL:0.8 mL
(1):1 + 4 ---LasI/LasR-GFP
(2):1 + 3 ---LasI/LuxR-GFP
(3):1 + 5 ---LasI/LuxR-RFP
(4):2 + 4 ---LuxI/LasI-GFP
(5):2 + 3 ---LuxI/LuxR-GFP
(6):2 + 5 ---LuxI/LuxR-RFP
(7):4 + flesh LB ---LasR-GFP
(8):3 + flesh LB ---LuxR-GFP
(9):5 + flesh LB ---LuxR-RFP