Difference between revisions of "Team:Waterloo/Parts"

Line 156: Line 156:
  
 
<div class="parts">
 
<div class="parts">
<div class="plasmid-group">
 
  <h2>Vectors</h2>
 
  <br>
 
  <br>
 
  <button v-on:click="show=1" class="plasmid plasmid1" >
 
    PSB1C3
 
  </button>
 
  <button v-on:click="show=2" class="plasmid plasmid2">
 
    PXP218
 
  </button>
 
  <button v-on:click="show=3"class="plasmid plasmid3" href="216">
 
  PXP216
 
  </button>
 
  </div>
 
 
<div v-for="plasmid in plasmids" v-if="plasmid.id == show">
 
<h2>^^plasmid.title$$</h2>
 
<div class="col-md-8 col-md-offset-2">
 
      <br>
 
      <br>
 
      <p>^^plasmid.text$$</p>
 
    </div>
 
 
</div>
 
  
 
   <h2>Parts</h2>
 
   <h2>Parts</h2>
Line 206: Line 182:
 
   </div>
 
   </div>
 
</div>
 
</div>
 +
 +
 +
 +
<div class="plasmid-group">
 +
  <h2>Vectors</h2>
 +
  <br>
 +
  <br>
 +
  <button v-on:click="show=1" class="plasmid plasmid1" >
 +
    PSB1C3
 +
  </button>
 +
  <button v-on:click="show=2" class="plasmid plasmid2">
 +
    PXP218
 +
  </button>
 +
  <button v-on:click="show=3"class="plasmid plasmid3" href="216">
 +
  PXP216
 +
  </button>
 +
  </div>
 +
 +
<div v-for="plasmid in plasmids" v-if="plasmid.id == show">
 +
<h2>^^plasmid.title$$</h2>
 +
<div class="col-md-8 col-md-offset-2">
 +
      <br>
 +
      <br>
 +
      <p>^^plasmid.text$$</p>
 +
    </div>
 +
 +
</div>
 +
 
</div>
 
</div>
 
</div>
 
</div>
Line 224: Line 228:
 
         id: 2,
 
         id: 2,
 
         title: "pXP218 (6226 bp)",
 
         title: "pXP218 (6226 bp)",
         text: "pXP218 is a modified pUC18 plasmid backbone used as a shuttle vector for yeast expression (Fang et al., 2011). It carries pBR322 and 2origins of replication as well as ampicillin resistance and URA3 nutrient-deficiency for both E. coli and S. cerevisiae expression (Fang et al., 2011). For our experiments, it was cut using the SpeI and SphI restriction sites, but it has a varied multiple cloning site."
+
         text: "pXP218 is a modified pUC18 plasmid backbone used as a shuttle vector for yeast expression (Fang et al., 2011). It carries pBR322 and 2µ origins of replication as well as ampicillin resistance and URA3 nutrient-deficiency for both E. coli and S. cerevisiae expression (Fang et al., 2011). For our experiments, it was cut using the SpeI and SphI restriction sites, but it has a varied multiple cloning site."
 
       },
 
       },
 
       {
 
       {
 
         id: 3,
 
         id: 3,
 
         title: "pXP216 (6115 bp)",
 
         title: "pXP216 (6115 bp)",
         text: "pXP216 is a modified pUC18 plasmid backbone used as a shuttle vector for yeast expression (Fang et al., 2011). It carries pBR322 and 2 origins of replication as well as ampicillin resistance and TRP1 nutrient-deficiency for both E. coli and S. cerevisiae expression (Fang et al., 2011). For our experiments, it was cut using the SpeI and SphI restriction sites, but it has a varied multiple cloning site."
+
         text: "pXP216 is a modified pUC18 plasmid backbone used as a shuttle vector for yeast expression (Fang et al., 2011). It carries pBR322 and origins of replication as well as ampicillin resistance and TRP1 nutrient-deficiency for both E. coli and S. cerevisiae expression (Fang et al., 2011). For our experiments, it was cut using the SpeI and SphI restriction sites, but it has a varied multiple cloning site."
 
       },
 
       },
 
     ],
 
     ],

Revision as of 01:40, 31 October 2017

Parts

Parts



^^item.text$$

Vectors



^^plasmid.title$$



^^plasmid.text$$