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Team:Freiburg/Notebook/18 August
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Add 1 μl Loading dye buffer and load the gel. | Add 1 μl Loading dye buffer and load the gel. | ||
| - | Take a picture of the gel, print picture and label the lanes! | + | Take a picture of the gel, print picture and label the lanes! <br/> |
[[File:Freigem18.8.11.jpg]] | [[File:Freigem18.8.11.jpg]] | ||
<br/> | <br/> | ||
Revision as of 14:27, 18 August 2011
Contact 
Contents |
green light receptor
Mutation PCR of CcaS
Investigators:Jakob
blue light receptor
NAME OF YOUR EXPERIMENT
Investigators:NAME
red light receptor
NAME OF YOUR EXPERIMENT
Investigators:NAME
Lysis cassette
NAME OF YOUR EXPERIMENT
Investigators:NAME
Precipitator
Miniprep
zymo Kit
| Name:Sophie
| Date:18.08.11 |
| Continue from Experiment: Cloning: ε5 was empty and the products from the cloning of 12.08.11 contain GFP-pbd too. (Date): 12.08.11
(Name): Sophie | |
| Project Name: inducible Promoter with pbd with cm-vector | |
Documentation:
Why are you doing this experiment? Name the parts which you extract.
ε5 was empty and the products from the cloning of 12.08.11 contain GFP-pbd too.
Name of the parts: GFP-pbd 4 4 4, GFP-pbd 4 1 3, GFP-pbd 6 6 8, GFP-pbd 4 2 2
Describe your results and mistakes and measure the DNA concentration with the Nanodrop and note the results.
| GFP-pbd 4 4 4: 164,1 ng/µl
GFP-pbd 4 1 3: 100,8 ng/µl GFP-pbd 6 6 8: 163,5 ng/µl GFP-pbd 4 2 2: 144,4 ng/µl |
How did you label your probes and where are they stored?
| Labelled GFP-pbd 4 4 4, GFP-pbd 4 1 3, GFP-pbd 6 6 8, GFP-pbd 4 2 2
stored in -20 until sequencing |
Testdigest
| Name: Sophie
| Date: 18.08.11 |
| Continue from Experiment: Miniprep (Date): 18.08.11
(Name): Sophie | |
| Project Name:inducible promoter for pbd with cm-vector | |
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 | 2,5 | |
| 0,5 μl | Enzym 2 | 2,5 | |
| 3 μl | DNA |
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.
Take a picture of the gel, print picture and label the lanes!
3A-assembly of IPTG-promoter, pbd-GFP and Cm-vector
Investigators: Sophie
Digestion
Amount of DNA and H20:
| Sample | DNA μl | H20 μl |
| IPTG-Promoter | 2,5 | 33 |
| GFP-pbd | 3 | 36 |
| pSB1A3 | 20 | 18 |
Enzymes necessary for digestion:
| GFP-pbd: 4 4 4 or 6 6 8 | IPTG-Promoter: S54 | vector: psB1C3 | |
| enzyme 1 | EcoRI | XbaI | EcoRI |
| enzyme 2 | NheI | PstI | PstI |
- Incubation at 37°C for 6 hours
- 20 minutes at 80°C
I won't continue with the IPTG-inducible-promoter-experiments because the part is shit.
We will work with a new IPTG-promoter
