Team:Groningen/Labwork/6 September 2013

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<br>ColonyPCR was performed on 6 colonies per plate (total of 12 colonies) beside one positive control (pSB1C3-S1). <br>The primers used were VF2 and VR (annealing temperature 56&deg;C).
<br>ColonyPCR was performed on 6 colonies per plate (total of 12 colonies) beside one positive control (pSB1C3-S1). <br>The primers used were VF2 and VR (annealing temperature 56&deg;C).
<br>The samples were checked on agarose gel 0.8%.
<br>The samples were checked on agarose gel 0.8%.
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<img src="https://static.igem.org/mediawiki/2013/6/69/ColonyPCR_pSB1C3-S1-S5.jpg" width="50%" >
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<br>pSB1C3-S1-S5 colonies.
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<img src="https://static.igem.org/mediawiki/2013/1/1f/ColonyPCR_pSB1C3-S2-S5.jpg" width="50%" >
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<br>pSB1C3-S2-S5 colonies.
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</div>

Revision as of 10:37, 6 September 2013

Claudio

The plates (pSB1C3-S1-S5 and pSB1C3-S2-S5) show single colonies.
ColonyPCR was performed on 6 colonies per plate (total of 12 colonies) beside one positive control (pSB1C3-S1).
The primers used were VF2 and VR (annealing temperature 56°C).
The samples were checked on agarose gel 0.8%.
pSB1C3-S1-S5 colonies.
pSB1C3-S2-S5 colonies.