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

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<h1>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. 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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<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>This includes usage of parts taken from: </p><ul><li>the T4 bacteriophage,</li><li> Cup1 from Yeast</li><li><li>CutA from E. coli</li> and elastin-like polymers (ELPs). </ul>
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<p>The regulators we are using are:</p><ul><li>a inducible promoter induced by IPTG(BBa_R0010)</li><li>a medium-strong Ribosomal-binding site(BBa_B0034)</li><li>and a double terminator(Bba_B0015)</li><br>  
  
 
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Revision as of 00:55, 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
    • and elastin-like polymers (ELPs).

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)