Team:TU-Eindhoven/Notebook/Week8

From 2012.igem.org

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<h3>Lab results</h3>
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[[File:device_testing_1.jpg|300px|right]]<h3>Lab results</h3>
The PCR-step and gel extraction for the BioBricks had to be redone because of mixed up microcentrifuge tubes. Furthermore, the restriction and ligation for the BioBricks are made. We made chlorampenicol plates and we transformed the Nova Blue E. coli with the ligation mix to obtain colonies carrying the BioBricks. But since we didn’t place the plates containing E. coli upside down, they dried out and the transformation failed. Therefore the transformation is repeated. Unfortunately, the BioBrick assembly of pSBIC3+GECO failed. We couldn’t find any colonies on the plates and in the bottles. To check the PCR product we used, we tested it on a gel. The gel showed that we got <span class= "red">the right inserts</span>. The problem seemed to be the ligation and restriction. A new PCR product of the GECOs is made as preparation for the assembly.  
The PCR-step and gel extraction for the BioBricks had to be redone because of mixed up microcentrifuge tubes. Furthermore, the restriction and ligation for the BioBricks are made. We made chlorampenicol plates and we transformed the Nova Blue E. coli with the ligation mix to obtain colonies carrying the BioBricks. But since we didn’t place the plates containing E. coli upside down, they dried out and the transformation failed. Therefore the transformation is repeated. Unfortunately, the BioBrick assembly of pSBIC3+GECO failed. We couldn’t find any colonies on the plates and in the bottles. To check the PCR product we used, we tested it on a gel. The gel showed that we got <span class= "red">the right inserts</span>. The problem seemed to be the ligation and restriction. A new PCR product of the GECOs is made as preparation for the assembly.  

Revision as of 19:51, 26 September 2012