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Team:Freiburg/Notebook/2 August
From 2011.igem.org
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Add 1 μl Loading dye buffer and load the gel. | Add 1 μl Loading dye buffer and load the gel. | ||
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===DNA Gel=== | ===DNA Gel=== | ||
Revision as of 11:20, 3 August 2011
Contact 
This is the wiki page of the Freiburger student team competing for iGEM 2011. Thank you for your interest!
Contents |
green light receptor
transformation with quickchanged CcaS
Investigators:Julia
Testdigest
Investigators:jakob, Julia
Testdigest
| Name:
Jakob | Date:
02.08.2011 |
| Continue from Experiment 02.08.2011
Miniprep | |
| Project Name: green light receptor, testdigest of CcaR with BamHI | |
For one reaction you need: For Mastermix: Number of samples+2extra
| 4μl | H2O | 20 | |
| 1μl | Buffer, NEB4 | 5 | |
| 1μl | BSA (10x) | 5 | |
| 0,5 μl | Enzym 1 | 1 | BamHI |
| 0,5 μl | Enzym 2 | - | |
| 3 μl | DNA | 3 |
10 μl total volume
Give 3 μl of DNA in an eppi and add 7μl of the mastermix.
Incubate for about 1h at 37°C.
Add 1 μl Loading dye buffer and load the gel.
DNA Gel
blue light receptor
NAME OF YOUR EXPERIMENT
Investigators:NAME
red light receptor
transformation with Ligationreaction(pcyA+terminator) from 1st of august and the pJT122
Investigators:Julia
Lysis cassette
NAME OF YOUR EXPERIMENT
Investigators:NAME
Precipitator
NAME OF YOUR EXPERIMENT
Investigators: NAME
