Difference between revisions of "Team:SCSU-New Haven/Results"

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<h1>Results</h1>
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You have the parts. You do the tests. You get the numbers. You say the numbers are good or bad. You plan your next steps.
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<h2>Parts Submitted</h2>
  
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<p>Here you can describe the results of your project and your future plans. </p>
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The only part we were able to submit was BBa_K2143000, our "Feedback" part. We felt it was our most useful part as there are already parts on the registry that use NahR and our part could work in conjunction with those parts.
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<h5>What should this page contain?</h5>
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</div><h2>Problems we encountered</h2>
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<li> Clearly and objectively describe the results of your work.</li>
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<li> Future plans for the project </li>
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<li> Considerations for replicating the experiments </li>
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<h5> Project Achievements </h5>
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<p>You can also include a list of bullet points (and links) of the successes and failures you have had over your summer. It is a quick reference page for the judges to see what you achieved during your summer.</p>
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<li>A list of linked bullet points of the successful results during your project</li>
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<li>A list of linked bullet points of the unsuccessful results during your project. This is about being scientifically honest. If you worked on an area for a long time with no success, tell us so we know where you put your effort.</li>
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<h5>Inspiration</h5>
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<p>See how other teams presented their results.</p>
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<li><a href="https://2014.igem.org/Team:TU_Darmstadt/Results/Pathway">2014 TU Darmstadt </a></li>
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<li><a href="https://2014.igem.org/Team:Imperial/Results">2014 Imperial </a></li>
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<li><a href="https://2014.igem.org/Team:Paris_Bettencourt/Results">2014 Paris Bettencourt </a></li>
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<p class="header_intro"> One of the biggest errors made was in the sequences we ordered. We put the biobrick prefixes and suffixes right the ends of the sequences without stuffer sequence. This meant we couldn't cut with EcoRI and PstI because there wasn't enough sequence for the enzymes to bind. Our solution was to cut with NotI, then check the direction of the insert. We later found out that the distributed linearized backbones have a base change in one of their NotI sites. This meat we had to take a plasmid, like BBa_J04450 and restrict it and purify the linear backbone, then digest our inserts, ligate and transform.
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</div><h2>Future Works</h2>
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<p class="header_intro">We'd like to finish cloning our parts and do the assays we designed. Once we establish the genetic device works, we'd then like to build a physical device to house the cells, as a handheld breathalyzer. We'd also like to look into other chassis that are able to persist for long periods without media. We felt a organism that forms spores would be best suited to this task such as Bacillus subtilis.
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Revision as of 01:13, 20 October 2016

SCSU IGEM SCSU iGEM

Results

You have the parts. You do the tests. You get the numbers. You say the numbers are good or bad. You plan your next steps.

Parts Submitted

The only part we were able to submit was BBa_K2143000, our "Feedback" part. We felt it was our most useful part as there are already parts on the registry that use NahR and our part could work in conjunction with those parts.

Problems we encountered

One of the biggest errors made was in the sequences we ordered. We put the biobrick prefixes and suffixes right the ends of the sequences without stuffer sequence. This meant we couldn't cut with EcoRI and PstI because there wasn't enough sequence for the enzymes to bind. Our solution was to cut with NotI, then check the direction of the insert. We later found out that the distributed linearized backbones have a base change in one of their NotI sites. This meat we had to take a plasmid, like BBa_J04450 and restrict it and purify the linear backbone, then digest our inserts, ligate and transform.

Future Works

We'd like to finish cloning our parts and do the assays we designed. Once we establish the genetic device works, we'd then like to build a physical device to house the cells, as a handheld breathalyzer. We'd also like to look into other chassis that are able to persist for long periods without media. We felt a organism that forms spores would be best suited to this task such as Bacillus subtilis.