Difference between revisions of "Team:Waterloo/Parts"

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<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Engagement"><span>Engagement</span></a></li>
 
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<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Societal_Considerations"><span>Societal Considerations</span></a></li>
 
<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Societal_Considerations"><span>Societal Considerations</span></a></li>
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<div class="row"><div class="col"><div class="content-main"><p>This year, our team biobricked the MetE gene into a cassette with LacI promoter:
 
<div class="row"><div class="col"><div class="content-main"><p>This year, our team biobricked the MetE gene into a cassette with LacI promoter:
 
<a href="http://parts.igem.org/Part:BBa_K2573000">BBa_K2573000</a>. This can be cloned into a methionine auxotroph to restore its ability to produce methionine. The MetE coding sequence can also be PCR amplified out of this biobrick and assembled into a new plasmid for a variety of applications. For instance, it can be put under the control of an optogenetic promoter/system (like CcaS/R or pDawn). </p>
 
<a href="http://parts.igem.org/Part:BBa_K2573000">BBa_K2573000</a>. This can be cloned into a methionine auxotroph to restore its ability to produce methionine. The MetE coding sequence can also be PCR amplified out of this biobrick and assembled into a new plasmid for a variety of applications. For instance, it can be put under the control of an optogenetic promoter/system (like CcaS/R or pDawn). </p>
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   <td> Name <td> Type <td> Description <td> Designer <td> length  
 
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     <td> <a href="http://parts.igem.org/Part:BBa_K2573000" > BBa_K2573000 </a> <td> Composite <td> MetE coding sequence in cassete with LacI promoter <td> Amanda Kuang  <td> 2658 </p>
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     <td> <a href="http://parts.igem.org/Part:BBa_K2573000" > BBa_K2573000 </a> <td> Composite <td> MetE coding sequence in cassete with LacI promoter <td> Amanda Kuang  <td> 2658  
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Revision as of 01:35, 18 October 2018

Parts

This year, our team biobricked the MetE gene into a cassette with LacI promoter: BBa_K2573000. This can be cloned into a methionine auxotroph to restore its ability to produce methionine. The MetE coding sequence can also be PCR amplified out of this biobrick and assembled into a new plasmid for a variety of applications. For instance, it can be put under the control of an optogenetic promoter/system (like CcaS/R or pDawn).

Name Type Description Designer length
BBa_K2573000 Composite MetE coding sequence in cassete with LacI promoter Amanda Kuang 2658