Difference between revisions of "Team:Waterloo/Parts"
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<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Experiments"><span>Experiments</span></a></li> | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Experiments"><span>Experiments</span></a></li> | ||
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<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Demonstrate"><span>Demonstrate</span></a></li> | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Demonstrate"><span>Demonstrate</span></a></li> | ||
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| − | <li class="dropdown nav-item"><a href="#" class="nav-link dropdown-toggle nav-link" data-toggle="dropdown" role="button" aria-haspopup="true" aria-expanded="false"> | + | <li class="dropdown nav-item"><a href="#" class="nav-link dropdown-toggle nav-link" data-toggle="dropdown" role="button" aria-haspopup="true" aria-expanded="false">Dry Lab<span class="caret"></span></a> |
<ul class="dropdown-menu"> | <ul class="dropdown-menu"> | ||
| + | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Model"><span>Model</span></a></li> | ||
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<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Software"><span>Software</span></a></li> | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Software"><span>Software</span></a></li> | ||
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| − | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/ | + | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Automation"><span>Automation</span></a></li> |
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| + | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Turbidostat"><span>Turbidostat</span></a></li> | ||
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</ul> | </ul> | ||
Revision as of 02:13, 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).