Team:Wageningen UR/Project/DevicesMeasuringOscillations
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(→Customary fluidic device designed by Team Wageningen UR to measure oscillations) |
(→Customary fluidic device designed by Team Wageningen UR to measure oscillations) |
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- | For the experiments, an overnight culture of the cells containing the relevant construct was spun down and resuspended in PBS. The resuspended culture was inoculated in the device and left | + | For the experiments, an overnight culture of the cells containing the relevant construct was spun down and resuspended in PBS. The resuspended culture was inoculated in the device and left the cells where left in the chamber to settle down for a while. Since the bacteria were bottom fed with LB as seen in the set up section in [[Team:Wageningen_UR/Project/DevicesSetup#Controlling_cell_growth| figure X+2]], only the bacteria which settled down in the wells survived, while the bacteria in PBS starved. This is shown in the short video below. The pictures were taken every ten minutes. |
[[File:PBS_cellgrowth_bottomfeed-1.tif|center]] | [[File:PBS_cellgrowth_bottomfeed-1.tif|center]] | ||
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The video shows the micro-dish directly after inoculation, when the bacteria are still floating around everywhere in the chamber. After that the bacteria which are only in PBS start to die, whereas the bacteria in the wells survive. | The video shows the micro-dish directly after inoculation, when the bacteria are still floating around everywhere in the chamber. After that the bacteria which are only in PBS start to die, whereas the bacteria in the wells survive. | ||
+ | After letting the bacteria grow in this manner for 2-3 hours, the PBS was removed with the same syringe that was used to inoculate. The chamber was then let to dry out over night. The two pictures seen below show the micro-dish with a ptet-GFP strain growing in the wells directly before and after removal of the PBS. | ||
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+ | [[File:ptetGFP_PBS.jpg|300px]][[File:ptetGFP_PBSremoved.jpg]] | ||
Revision as of 12:32, 19 September 2011