Team:Wageningen UR/Notebook/Proj1/July
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- | The | + | Cultures were put in a shake incubator at 30°C, 300 rpm. |
+ | The OD600s of every culture were measured 2 hours after inoculation and subsequently each hour, by taking 1 mL samples from the culture. the OD was measured with a Hitachi U1500 spectrophotometer. LB+amp was taken as blank. | ||
Fluorescence was measured in a 96-wells plate on a fluorescent plate reader (Molecular Devices, M2 (toxicology). First blank measurements were done with 96 wells plates containing 50 ul LB+amp. The output corresponding with the specific wells was saved and used for further calculations. | Fluorescence was measured in a 96-wells plate on a fluorescent plate reader (Molecular Devices, M2 (toxicology). First blank measurements were done with 96 wells plates containing 50 ul LB+amp. The output corresponding with the specific wells was saved and used for further calculations. | ||
Revision as of 10:31, 30 July 2011
Building a Synchronized Oscillatory System
July - Synchronized Oscillatory System