Difference between revisions of "Team:Uppsala"

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                             <p><b>-</b> The first step was to obtain live nematodes by the recovery of the eggs from the feces. After this process the large strongyles were divided from the small strongyles using a 3D printed microfluidic chip or a microscope and stored for successive use.<br><br><b>Figure 1:</b>Flowchart representing the worm culturing outline.</p>
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                             <p>The first step was to obtain live nematodes by the recovery of the eggs from the feces. After this process the large strongyles were divided from the small strongyles using a 3D printed microfluidic chip or a microscope and stored for successive use.<br><br><b>Figure 1:</b>Flowchart representing the worm culturing outline.</p>
 
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                             <p><b>-</b> After receiving the results from either the transcriptomics or the phage display, they need to be combined with a reported to get a functioning diagnostic tool (Worm Buster).  We have adapted and troubleshot the expression of a fluorescent chromoprotein, UnaG, to be able to detect our worms in both the intestines and in feces. This would enable a relatively simple and quantitative way for ranchers to detect the worms of interest, using a cheap UV lamp, a dark room, and a camera!<br><br>
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                             <p>After receiving the results from either the transcriptomics or the phage display, they need to be combined with a reported to get a functioning diagnostic tool (Worm Buster).  We have adapted and troubleshot the expression of a fluorescent chromoprotein, UnaG, to be able to detect our worms in both the intestines and in feces. This would enable a relatively simple and quantitative way for ranchers to detect the worms of interest, using a cheap UV lamp, a dark room, and a camera!<br><br>
 
                     In order to make this a viable reporter system, we wanted to make sure the original biobrick part was functional.  We show how we tweaked this part in order to study if it works properly so that it could be potentially used in future studies.<br><br><b>Figure 4: </b>We would be able to detect the wormd in feces with this method.</p>
 
                     In order to make this a viable reporter system, we wanted to make sure the original biobrick part was functional.  We show how we tweaked this part in order to study if it works properly so that it could be potentially used in future studies.<br><br><b>Figure 4: </b>We would be able to detect the wormd in feces with this method.</p>
 
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Revision as of 11:48, 16 October 2018




Uppsala iGEM 2018