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− | <p> | + | <p>A team member visited a government "biotechnology park" intended to be used by small scale startups. We wanted to understand the facilities available in these parks to see if there existed a need for improvement and gauge the feasibility of implementing our project in these parks. We found that the bioreactors in these parks had no sensors, centrifuges or any level of automation. These bioreactors were currently used only to grow cultures that were sold without further processing. |
− | + | We input information learned from our visit into our project by developing biobricks and a protocol to perform functions usually done by machines, which were not available in these parks like centrifugation, automatic induction and cell density monitoring. This would enable more complicated protocols required for the biosynthesis of most useful products to be undertaken at these facilities. </p> | |
+ | <p>Thus, we integrated information gleaned from the visit in the processes targeted by cellfifuge.</p> | ||
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Revision as of 19:35, 14 October 2016
A team member visited a government "biotechnology park" intended to be used by small scale startups. We wanted to understand the facilities available in these parks to see if there existed a need for improvement and gauge the feasibility of implementing our project in these parks. We found that the bioreactors in these parks had no sensors, centrifuges or any level of automation. These bioreactors were currently used only to grow cultures that were sold without further processing. We input information learned from our visit into our project by developing biobricks and a protocol to perform functions usually done by machines, which were not available in these parks like centrifugation, automatic induction and cell density monitoring. This would enable more complicated protocols required for the biosynthesis of most useful products to be undertaken at these facilities.
Thus, we integrated information gleaned from the visit in the processes targeted by cellfifuge.