Difference between revisions of "Team:Lethbridge HS/Parts"

 
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      <div style="font-family: 'Montserrat' , serif;font-size: 10vw;text-align:center;margin-top:50px;"><center>PARTS OVERVIEW</center></div>
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<center><div style="font-family: 'Montserrat' , serif;font-size: 9vw;text-align:center;margin-top:50px;"><center>PARTS OVERVIEW</center></div>
  
 
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<h1  style="font-size: 25px; font-family:Montserrat;"class="w100" ><b>Parts Used</b></h1>
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<p style="font-size: 18px; font-family: 'Open Sans'">For our project we are using parts primarily serving the function of capturing ions, holding on to them and precipitating out of solution. This includes usage of parts taken from the T4 bacteriophage, Cup1/CutA from E. coli, and elastin-like polymers. The regulators we are using are: a inducible promoter induced by IPTG(BBa_R0010), a medium-strong Ribosomal-binding site(BBa_B0034) and a double terminator(Bba_B0015) to ensure transcription ends. </p> <br>  
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<h1  style="font-size: 3vw; font-family:Montserrat;"class="w100" >CU LATER PARTS OVERVIEW</h1>
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<p style="font-size: 18px; font-family: 'Open Sans'">For our project we are using parts primarily serving the function of capturing ions, holding on to them and precipitating out of solution. </p><p style="font-size: 18px; font-family: 'Open Sans'">This includes usage of parts taken from: </p style="font-size: 18px; font-family: 'Open Sans'"><ul style="font-size: 18px; font-family: 'Open Sans'"><li>the T4 bacteriophage</li><li> Cup1 from Yeast</li><li>CutA from <i>E. coli</i></li> <li>elastin-like polymers (ELPs). </li></ul>
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<p style="font-size: 18px; font-family: 'Open Sans'">The regulators we are using are:</p><ul style="font-size: 18px; font-family: 'Open Sans'"><li>an inducible promoter induced by IPTG(BBa_I712074)</li><li>a medium-strong ribosomal-binding site(BBa_J61100)</li><li>and a double terminator(BBa_B0014)</li></ul><br>  
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Latest revision as of 03:33, 18 October 2018



CU LATER PARTS OVERVIEW

For our project we are using parts primarily serving the function of capturing ions, holding on to them and precipitating out of solution.

This includes usage of parts taken from:

  • the T4 bacteriophage
  • Cup1 from Yeast
  • CutA from E. coli
  • elastin-like polymers (ELPs).

The regulators we are using are:

  • an inducible promoter induced by IPTG(BBa_I712074)
  • a medium-strong ribosomal-binding site(BBa_J61100)
  • and a double terminator(BBa_B0014)