Team:Aachen/Safety
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- | To detect ''P. aeruginosa'' cells, a sampling agar chip is slightly pressed against the solid surface to be tested. Afterwards, the sampling chip is immediately introduced into our measurement device and will not be removed until the detection is finished and the chips | + | To detect ''P. aeruginosa'' cells, a sampling agar chip is slightly pressed against the solid surface to be tested. Afterwards, the sampling chip is immediately introduced into our measurement device and will not be removed until the detection is finished and the chips has been disinfected. The sensor chips must be handled in '''S1 environments only''' since they contain genetically modified ''E. coli''. However, once introduced into the measurement device, the sensor chips, too, will not be removed before disinfection. The living cells inside the measurement device are effectively killed after a measurement by '''using desinfectants''' such as Bacillol. For this procedure, the drawer of the measurement device is opened and Bacillol is poured over the sampling and sensor chips. Afterwards, both chips can be autoclaved and disposed. The whole lining of the measurement device is built from plastic so that it can be disinfected easily. |
To '''simulate the worst case scenario''', we did replica plating of some exemplary sensor chips. In three experiments, we got an arithmetic mean of five colonies which were picked up. From that we concluded that the '''risk of infection is really low''' even if the measurement device and chips are not handled properly. | To '''simulate the worst case scenario''', we did replica plating of some exemplary sensor chips. In three experiments, we got an arithmetic mean of five colonies which were picked up. From that we concluded that the '''risk of infection is really low''' even if the measurement device and chips are not handled properly. | ||
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Revision as of 01:32, 17 October 2014
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