Team:Evry/Interlab Study/09-02-2014

From 2014.igem.org

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<h2>Construction n°1: PSB1C3 with I20260</h2>
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<br/><h2>Construction n°1: PSB1C3 with I20260</h2>
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Analyse of sequencing results. The two constructions were ok although the colony 4 had a better match. So we decided to keep this colony to perform promoter activity assays.
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<h2>Constructions with other promoters</h2>
<h2>Constructions with other promoters</h2>
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Miniprep cultures from the 2cnd of september was purified with the NucleoSpin Plasmid kit (Macherey-Nagel). DNA was quantify with the Nanodrop 2000
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Miniprep cultures from the 2cnd of september was purified with the NucleoSpin Plasmid kit (Macherey-Nagel). DNA was quantify with the Nanodrop 2000.
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<br/> Glycerol stock were prepared started from the 16 cultures from the 2cnd of september (750 µl of culture + 750 µL of 10% glycerol) and stored at -80°C.
<span class="cd-date">Sep 02</span>  
<span class="cd-date">Sep 02</span>  

Revision as of 18:32, 17 September 2014

Picture


Construction n°1: PSB1C3 with I20260


Analyse of sequencing results. The two constructions were ok although the colony 4 had a better match. So we decided to keep this colony to perform promoter activity assays.

Construction n°2: PSB1C3 with J23101-E1010




Construction n°3: PSB1C3 with K823012-E1010



Constructions with other promoters


Miniprep cultures from the 2cnd of september was purified with the NucleoSpin Plasmid kit (Macherey-Nagel). DNA was quantify with the Nanodrop 2000.
Glycerol stock were prepared started from the 16 cultures from the 2cnd of september (750 µl of culture + 750 µL of 10% glycerol) and stored at -80°C. Sep 02