IGEM:Groningen/Notebook/iGEM 2011/2011/06/28: Difference between revisions

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==Entry title==
==28-6-11==
* Insert content here...


<br>
<br> Colony PCR PhybB RBS GFP DT
<br> Taq 10× buffer: 20μl
<br> dNTPs 10mM: 4μl
<br> MgCl2: 12μl
<br> Forward Biobrick primer: 4μl
<br> Reverse Biobrick primer: 4μl
<br> Taq DNA polymerase: 1μl
<br> MQ water: 155μl
<br>
<br> PCR conditions:
<br> Preheated lid: 111°C
<br> Denaturation: 94°C for 10 min.
<br> Cycle 33×:
<br>  denaturation: 94°C for 30s.
<br>  annealing:    60°C for 30s.
<br>  Extension:    72°C for 2,5 min.
<br> Final extension: 72°C for 10 min.
<br> Store infinite at 4°C
<br>
<br> Analyse on a 1% TBE agarose gel.
<br>
<br> Making plan for parallel cloning work
<br>
<br> Helping with sponsoring and doing some Human practices work
<br>
<br>


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Revision as of 03:49, 21 September 2011

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28-6-11



Colony PCR PhybB RBS GFP DT
Taq 10× buffer: 20μl
dNTPs 10mM: 4μl
MgCl2: 12μl
Forward Biobrick primer: 4μl
Reverse Biobrick primer: 4μl
Taq DNA polymerase: 1μl
MQ water: 155μl

PCR conditions:
Preheated lid: 111°C
Denaturation: 94°C for 10 min.
Cycle 33×:
denaturation: 94°C for 30s.
annealing: 60°C for 30s.
Extension: 72°C for 2,5 min.
Final extension: 72°C for 10 min.
Store infinite at 4°C

Analyse on a 1% TBE agarose gel.

Making plan for parallel cloning work

Helping with sponsoring and doing some Human practices work