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

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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.  
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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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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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<img class="img-fluid"style="float:right; margin-left:15px;margin-bottom:5px;
 
      
 
      

Revision as of 01:01, 17 October 2018

Parts Used

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.