BIOTEC Dresden/Notepad/30 August 2010
From 2010.igem.org
(Difference between revisions)
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The whole ligation reaction was used for electroporation. | The whole ligation reaction was used for electroporation. | ||
+ | '''AHL Sensor''' | ||
+ | |||
+ | <p>AHL plate reader assay was done with part 24f. A pipetting scheme was used where different concentrations of the stock solution was used (from 0.015µM to 150µM) in LB.</p> | ||
+ | |||
+ | <p>Measurement of part 17e for 3 hours using AHL concentrations of (0.01-2000nM) | ||
{{Biotec_Dresden/month}} | {{Biotec_Dresden/month}} | ||
{{Biotec_Dresden/Bottom}} | {{Biotec_Dresden/Bottom}} |
Revision as of 16:13, 27 October 2010
Fusion Protein
The ligation was set up again. Due to low plasmid concentrations only luxI-proteinA fusions were performed. Different molar ratios 1:1 and 1:3 were used. This time also control ligations using only the digested plasmid were carried out. Ligation reactions were incubated at room temperature for 1 hour. The whole ligation reaction was used for electroporation.
AHL Sensor
AHL plate reader assay was done with part 24f. A pipetting scheme was used where different concentrations of the stock solution was used (from 0.015µM to 150µM) in LB.
Measurement of part 17e for 3 hours using AHL concentrations of (0.01-2000nM)
July |
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August |
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September |
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October |
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