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

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<h1  style="font-size: 4vw; 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>  
 
<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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Revision as of 03:01, 17 October 2018



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.