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Team:Heidelberg/Notebook/Sensing Group/Notebook/11thweek
From 2008.igem.org
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== Wednesday, 10/15/2008 == | == Wednesday, 10/15/2008 == | ||
| + | * PCR Purification of LuxS_standard and F1-GeneArt, F2-GeneArt | ||
| + | * Digestion of LuxS and Fusion Constructs with EcoRI/PstI (NEBuffer EcoRI + BSA) | ||
| + | * Digestion of LuxS with EcoRI/xbaI (NEBuffer2 + BSA) to check for restriction sites | ||
| + | * Cloning into pSB2K3 | ||
| + | * Test Digestion of LuxS with EcoRI and xbaI to test if mutation was successful | ||
| + | * Digestion of Fusion1-YFP and Fusion2-YFP constructs with BamHI | ||
| + | [[Image:HD 081015-LuxS Digestion.png|left|thumb|300px|LuxS digestions with EcoRI and xbaI to test for successful mutagenesis]][[Image:HD 081015-LuxS Fusion-YFP Digestions.png|left|thumb|200px|Digestion of LuxS to test for mutations and Fusion-YFP with BamHI constructs to confirm insert.] | ||
| + | |||
| + | * Inoculation of 50µl Fusion-YFP O/N culture in 5mL LB. Incubation for 2h @ 37°C. Induction of Fusion-YFP cells with 0.01% Arabinose for 3h. Visualization under microscope | ||
| + | Expression of Fusion-Receptor positive for both constructs. Even Localization to the membrane can be seen in some cells. | ||
== Thursday, 10/16/2008 == | == Thursday, 10/16/2008 == | ||
== Friday, 10/17/2008 == | == Friday, 10/17/2008 == | ||
Revision as of 19:51, 26 October 2008
Contents |
Monday, 10/13/2008
- Miniprep of LuxS_mut_EcoRI and F1-YFP, F2-YFP
- Digestion of Fusion-YFP with BamHI (NEBuffer3 + BSA)
- Insert: 5937 bp and 1998 bp
- No Insert: 7202 bp
- Digestion of LuxS with EcoRI/NdeI (NEBuffer EcoRI)
- Insert: 2773 bp and 1862 bp
- 4635 bp
- Fusion-PCR for LuxS standardization with Phusion
- 30s @ 98°C || 10s @ 98°C | 30s @ 55°C | 1min @ 72°C || 5min @ 72°C | 4°C (30 cycles)
Tuesday, 10/14/2008
- PCR Purification, Digestion of LuxS and pSB2K3 with EcoRI/PstI (EcoRI buffer + BSA). 1h @ 37°C
- Fusion PCR for LuxS with Phusion and Annealing Temperature Gradient (50-60°C)
- Transformation of Fusion-YFP into MG1655
Wednesday, 10/15/2008
- PCR Purification of LuxS_standard and F1-GeneArt, F2-GeneArt
- Digestion of LuxS and Fusion Constructs with EcoRI/PstI (NEBuffer EcoRI + BSA)
- Digestion of LuxS with EcoRI/xbaI (NEBuffer2 + BSA) to check for restriction sites
- Cloning into pSB2K3
- Test Digestion of LuxS with EcoRI and xbaI to test if mutation was successful
- Digestion of Fusion1-YFP and Fusion2-YFP constructs with BamHI
- Inoculation of 50µl Fusion-YFP O/N culture in 5mL LB. Incubation for 2h @ 37°C. Induction of Fusion-YFP cells with 0.01% Arabinose for 3h. Visualization under microscope
Expression of Fusion-Receptor positive for both constructs. Even Localization to the membrane can be seen in some cells.
