Team:SCU-China/Transmitter

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<li ><a href="#1">Week 1 8.21-8.24</a></li>
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<li ><a href="#1">Week 1</a></li>
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<li ><a href="#2">Week 2 8.25-8.31</a></li>
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<li ><a href="#2">Week 2</a></li>
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<li ><a href="#3">Week 3</a></li>
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<li ><a href="#4">Week 4</a></li>
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<li ><a href="#5">Week 5</a></li>
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<ol style="list-style-type: lower-latin;">
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<p>Since our team is sorted into 4 groups, our team is focusing on the construction of the Transmitter Cell. The whole work that we should do is to build 2 gene lines which lie in the transmitter cells.</p><p>In detail, we use 9 biobricks supplied by IGEM Competition totally which are RBS (BBa_B0030), DT (BBa_B0015), pLux (BBa_R0062), LuxR (BBa_C0062), LasI (BBa_K081016 and BBa_K081009), CinR (BBa_K0077), RhlR (BBa_C0171), and RhlI (BBa_C0051).</p><h1 id="1" style="padding-top: 80px;
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<li>Notebook of Effector Group</p><p>Since our team are sorted into different groups, we are focusing on constructing the Effector Cell. Totally, we should build 3 different effector cells to fulfill our project. In detail, we make use of the following biobricks to construct the effector cells. They are pLas (BBa_R0079), Constitutive Promoter (BBa_J23106), pLas/lux (BBa_K091146), RBS (BBa_B0034), RFP (BBa_E1010), amilCP (BBa_K592009), cjBlue (BBa_K592011), LasR (BBa_C0079), DT (BBa_B0015).</p><p>Week 1 7.17-7.20</p><p>1. We transformed the plasmids (BBa_R0079, BBa_J23106, BBa_K091146, BBa_B0034, BBa_E1010, BBa_K592009, BBa_K592011, BBa_C0079, BBa_B0015) to amplify them.</p><p>2. We extracted the plasmids (mentioned above) and did the electrophoresis to test the quality and concentration of them.</p><p>Results</p><p>The concentration of Plasmids</p><table><tr><td><p>Name</li>
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  margin-top: -45px;">Week 1 7.20-7.26</h1><p>1. We transformed the plasmids (BBa_B0030, BBa_B0015, BBa_R0062, BBa_K081016, BBa_K081009, BBa_K0077, BBa_C0171, BBa_C0051) into DH5&#945; E.Coli to amplify these plasmid</p><p>We extracted the plasmids (mentioned above) and used electrophoresis to test the concentration and quality of our plasmids.</p><p>Results:</p><table class="table table-striped"><thead><tr><td><p>Name</li>
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</ol>
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</ol>
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</td><td><p>Concentration (ng/3 &#956;l)</p>
</td><td><p>Concentration (ng/3 &#956;l)</p>
</td>
</td>
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</tr><tr><td><p>BBa_J23106</p>
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</tr></thead><tbody><tr><td><p>BBa_R0062</p>
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</td><td><p>Failed</p>
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</td><td><p>53.3/ 43.5</p>
</td>
</td>
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</tr><tr><td><p>BBa_R0079</p>
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</tr><tr><td><p>BBa_K081016</p>
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</td><td><p>168.2/106.4</p>
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</td><td><p>107.9/ 176.7</p>
</td>
</td>
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</tr><tr><td><p>BBa_K091146</p>
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</tr><tr><td><p>BBa_B0030</p>
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</td><td><p>114.1/86.4</p>
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</td><td><p>28.2,/8.96</p>
</td>
</td>
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</tr><tr><td><p>BBa_B0034</p>
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</tr><tr><td><p>BBa_C0171</p>
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</td><td><p>97.6/96.5/79.5</p>
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</td><td><p>322.6/ 387.5</p>
</td>
</td>
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</tr><tr><td><p>BBa_E1010</p>
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</tr><tr><td><p>BBa_K0077</p>
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</td><td><p>116.5/118.5</p>
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</td><td><p>193.4,/143.9</p>
</td>
</td>
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</tr><tr><td><p>BBa_K592009</p>
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</tr><tr><td><p>BBa_K081009</p>
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</td><td><p>129.3/95.2</p>
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</td><td><p>64.4,/63.1</p>
</td>
</td>
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</tr><tr><td><p>BBa_K592011</p>
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</tr><tr><td><p>BBa_C0077</p>
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</td><td><p>135/114.9</p>
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</td><td><p>152.7/ 156</p>
</td>
</td>
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</tr><tr><td><p>BBa_C0079</p>
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</tr><tr><td><p>BBa_C0062</p>
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</td><td><p>196.1/182.6</p>
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</td><td><p>53.29/128.7</p>
</td>
</td>
</tr><tr><td><p>BBa_B0015</p>
</tr><tr><td><p>BBa_B0015</p>
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</td><td><p>95.8/86.1/231.2</p>
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</td><td><p>116.2/19.5</p>
</td>
</td>
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</tr>
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</tr></tbody>
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</table><ol>
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</table>
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<ol style="list-style-type: lower-latin;">
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<p>Note: The different concentrations are from different tubes.</p><h1 id="2" style="padding-top: 80px;
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<li>Note: Different concentrations are from different tubes.</p><p>Week 2 7.21-7.27</p><p>1. We picked up colonies from the plates made last time and did the liquid culture of bacteria that contain the plasmid (mentioned above).</p><p>2. We stored the bacteria that contain plasmids (mentioned above) with glycerol in -80&#8451;.</p><p>3. We extracted the plasmids again.</p><p>4. We cleaved the plasmids (BBa_B0034 and BBa_K592011) in 37&#8451;.</p><p>Results</p><p>1. For plasmids prep, the concentration was too low and we discarded them.</p><p>2. For cleavage, there was no line appearing on gel.</p><p>Week 3 7.28-8.03</p><p>1. We transformed BBa_I71204, BBa_I1466, BBa_K575014, BBa_J23100, BBa_I718013, BBa_K592025, BBa_S03156, BBa_I13401, BBa_C0171 plasmids into E.Coli and extracted the plasmids.</p><p>2. We cleaved the plasmids mentioned above by the EcoR I and Spe I (BBa_I13401, BBa_S03156, BBa_B0015, BBa_I1466, BBa_K592025) or Xba I and Pst I (BBa_J23100, BBa_C0171, BBa_K575014).</p><p>3. We tested our cleavage products by electrophoresis.</p><p>Results</p><p>The concentration of plasmids</p><table><tr><td><p>Name</li>
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  margin-top: -45px;">Week 2 7.27-8.03</h1><p>1. We transformed the BBa_C0062 and BBa_C0077 plasmids.</p><p>2. We extracted the BBa_J37019, BBa_I9026, BBa_K081005, BBa_I714075, BBa_K93600 and BBa_R0077 plasmids and determined the concentration of them by electrophoresis.</p><p>3. We cleaved the BBa_R0062, BBa_C0051, BBa_K0077 plasmids with EcoR I and Spe I enzyme and BBa_B0015 with Xba I and Pst I. Also, we prepared the pSB1A3 and pSB1K3 backbones with EcoR I and Pst I.</p><p>4. We cleaved the BBa_J37019 (Named E11) and BBa_R0077 (E21) with EcoR I and Spe I, BBa_I9026 (E12), BBa_K081016 (E22) and BBa_C0077 (E24) with Xba I and Pst I.</p><p>5. We linked the E11 and E12 with pSB1A3 (L11), the E21 and E22 with pSB1A3 (L21).</p><p>6. We transformed all the linked parts into E.coli.</p><p>7. We cleaved BBa_B0015 with Xba I and Pst I.</p><p>Results</p><table class="table table-striped"><caption>The concentration of plasmids</caption><thead><tr><td><p>Name</li>
-
</ol>
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-
</ol>
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</td><td><p>Concentration (ng/3&#956;l)</p>
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</td><td><p>Concentration (ng/3 &#956;l)</p>
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</td>
</td>
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</tr><tr><td><p>BBa_K575014</p>
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</tr></thead><tbody><tr><td><p>BBa_J37019</p>
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</td><td><p>61.9/56.6</p>
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</td><td><p>400/403</p>
</td>
</td>
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</tr><tr><td><p>BBa_I1466</p>
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</tr><tr><td><p>BBa_I9026</p>
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</td><td><p>42.8/41.3</p>
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</td><td><p>247/140.6</p>
</td>
</td>
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</tr><tr><td><p>BBa_I13401</p>
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</tr><tr><td><p>BBa_R0077</p>
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</td><td><p>51.3/48.6</p>
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</td><td><p>134/161.2</p>
</td>
</td>
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</tr><tr><td><p>BBa_C0171</p>
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</tr><tr><td><p>BBa_K081005</p>
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</td><td><p>70.4/89.0</p>
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</td><td><p>51.2/27.6</p>
</td>
</td>
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</tr><tr><td><p>BBa_S03156</p>
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</tr><tr><td><p>BBa_I714075</p>
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</td><td><p>88.0/84.3</p>
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</td><td><p>95.7/37.2</p>
</td>
</td>
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</tr><tr><td><p>BBa_K592025</p>
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</tr><tr><td><p>BBa_K93600</p>
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</td><td><p>73.3/111.9</p>
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</td><td><p>41.6</p>
</td>
</td>
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</tr><tr><td><p>BBa_J23100</p>
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</tr><tr><td><p>L1</p>
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</td><td><p>59.6/185.5</p>
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</td><td><p>92.3/54.2</p>
</td>
</td>
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</tr><tr><td><p>BBa_I1718013</p>
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</tr><tr><td><p>L2</p>
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</td><td><p>68.0/52.0</p>
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</td><td><p>88.4/60.4</p>
</td>
</td>
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</tr><tr><td><p>BBa_I71204</p>
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</tr></tbody>
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</td><td><p>59.7/22.9/54.3</p>
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</table>
 +
<li>Note: The different concentrations are from different tubes.</p><p>2. The electrophoresis results are shown in Figure 1.</p>
 +
<img src="https://static.igem.org/mediawiki/2014/2/24/T1.png">
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<p>Figure 1. The cleaved plasmids</p><h1 id="3" style="padding-top: 80px;
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  margin-top: -45px;">Week 3 8.04-8.10</h1><p>1. We linked the L1 and BBa_B0015 with pSB1T3 (named F1), L2 and BBa_I9026 with pSB1T3 (F2). Then we transformed them into E.coli to amplify them and we extracted the plasmids to test their quality.</p><p>2. We linked E11 and E12 with pSB1T3 (named LA1), E21 and E22 with pSB1A3 (LA2).</p><p>3. We cleaved the BBa_J37019 (Named E11) and BBa_R0077 (E21) with EcoR I and Spe I, BBa_I9026 (E12), BBa_K081016 (E22) and BBa_C0077 (E24) with Xba I and Pst I again and tested their qualities by electrophoresis and then we did the gel purification.</p><p>4. We cleaved the BBa_R0077 with Spe I and Pst I (named EP21).</p><p>5. We linked EP21 and E22 with 3 different backbones (pSB1T3, pSB1A3, and pSB1C3) which are tested by electrophoresis.</p><p>Results:</p><table class="table table-striped"><caption>The concentration of plasmids and linkage product</caption><thead><tr><td><p>Name</li>
 +
 
 +
</td><td><p>Concentration (ng/3&#956;l)</p>
</td>
</td>
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</tr>
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</tr></thead><tbody><tr><td><p>F11&#9;</p>
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</table><ol>
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</td><td><p>Failed</p>
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<ol style="list-style-type: lower-latin;">
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<li>Note: Different concentrations are from different tubes</p><p>2. The electrophoresis result is shown in Figure 1.</p><p>Figure 1. The cleavage results of plasmids</p><p>Week 4 8.04-8.10</p><p>1. We cleaved the backbones with Kanamycin and Ampicillin resistance.</p><p>2. We linked the biobricks with our backbones via 3A assembly. In detail, we linked the BBa_B0015 and BBa_C0171 with pSB1A3 (named A1); the BBa_B0015 and BBa_K575014 with pSB1A3 (A2); the BBa_S03156 and BBa_J23100 with pSB1K3 (K1); and the BBa_I1466 and BBa_J23100 with pSB1K3 (K2).</p><p>3. We transformed our linkage products into E.coli. and did the liquid culture to amplify the products. And then we extracted the plasmids which are tested by cleavage and electrophoresis.</p><p>4. We cleaved the pSB1C3 serving as the backbones to link A2 with K2 (C1) and A1 with K1 (C2).</p><p>5. We linked the BBa_K592025 and BBa_B0015 with pSB1A3 (A3).</p><p>6. We cleaved BBa_K592025 and BBa_B0015.</p><p>Results</p><p>The concentration of plasmids</p><table><tr><td><p>Name</li>
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-
</ol>
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-
</ol>
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-
</td><td><p>Concentration (ng/3 &#956;l)</p>
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</td>
</td>
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</tr><tr><td><p>A1</p>
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</tr><tr><td><p>F21</p>
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</td><td><p>86.7/39.3</p>
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</td><td><p>failed</p>
</td>
</td>
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</tr><tr><td><p>A2</p>
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</tr><tr><td><p>E11</p>
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</td><td><p>41.0/23.7</p>
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</td><td><p>8.53</p>
</td>
</td>
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</tr><tr><td><p>K1</p>
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</tr><tr><td><p>E12</p>
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</td><td><p>37.3</p>
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</td><td><p>Failed</p>
</td>
</td>
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</tr><tr><td><p>K2</p>
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</tr><tr><td><p>E21</p>
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</td><td><p>18.2/103.0</p>
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</td><td><p>24.9/7.5</p>
</td>
</td>
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</tr>
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</tr><tr><td><p>E22</p>
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</table><ol>
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</td><td><p>14/5.3</p>
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<ol style="list-style-type: lower-latin;">
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</td>
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<li>Note: The different concentrations are from different tubes</p><p>2. <img width="40" height="36" src="Notebook of Effector(1).files/Notebook of Effector(1)3342.png"><img width="28" height="31" src="Notebook of Effector(1).files/Notebook of Effector(1)3343.png">The electrophoresis result is shown in Figure 2.</p><p>Figure 2. A the cleaved backbones (pSB1K3 and pSB1A). B and C the cleaved plasmids.</p><p>Week 5 8.11-8.17</p><p>1. We linked the BBa_K592025 and BBa_B0015 with pSB1A3 (Named Li3).</p><p>2. We transformed the BBa_K608002, BBa_K082035, and Li3.</p><p>3. We cleaved A1, A2, K1, K2 to test their qualities.</p><p>4. We did the liquid culture of C1, BBa_K608002, BBa_K082035, K3, C2, BBa_I1466, BBa_B0015, and BBa_J23100 and extracted these plasmids and tested the quality of C1 by cleavage and electrophoresis.</p><p>5. We cleaved K1, A3, BBa_J23100, BBa_K575014, and BBa_C0171 with EcoR I and Spe I; A1; BBa_K608002, BBa_S03156, BBa_B0015, BBa_I1466, and BBa_K592025 with Xba I and Pst I .</p><p>6. We linked the K1 and A1 with pSB1C3 (C2), A2 and K2 with pSB1C3 (C1), A3 and BBa_K608002 with pSB1K3 (K3), BBa_B0015 and BBa_C0171 with pSB1A3 (named A1); the BBa_B0015 and BBa_K575014 with pSB1A3 (A2); the BBa_S03156 and BBa_J23100 with pSB1K3 (K1); and the BBa_I1466 and BBa_J23100 with pSB1K3 (K2) and then we transformed them to extract the plasmids and tested them by cleavage.</p><p>7. We prepared the pSB1K3, pSB1A3, and pSB1C3 by EcoR I and Pst I.</p><p>Results</p><p>1. The electrophoresis result is shown in Figure 3.</p><p>Figure 3. A and B the cleaved A1, A2, and K1, K2. C and D the cleaved plasmids. E the cleaved backbones and plasmids.</p><p>Week 5 8.18-8.24</p><p>1. We cleaved the K1, K2, BBa_R0040 and pSB1T3 with proper enzyme</p><p>2. We linked the A2 and K2 with pSB1C3 (C1), the BBa_R0040and BBa_S03156 with pSB1A3 (A4 and A5), the K1 and A1 with pSB1T3 (T2), the K1 and A1 with pSB1C3 (C2). And then we transformed them to extract the plasmids.</p><p>3. We extracted C1 plasmids and tested them with cleavage.</p><p>4. We transformed BBa_K575037 and BBa_K575039 to extract the plasmids.</p><p>5. We linked BBa_K575037, BBa_K575039 with CP, Blu, R, and C2 respectively.</p><p>Results</p><p><img width="44" height="39" src="Notebook of Effector(1).files/Notebook of Effector(1)5152.png"><img width="67" height="45" src="Notebook of Effector(1).files/Notebook of Effector(1)5153.png">The electrophoresis result is shown in Figure 4.</p><p>Figure 5. A, B, and C. the cleaved plasmids D. the intact plasmids.</p><p></li>
+
</tr><tr><td><p>E24</p>
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</ol>
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</td><td><p>18.1/17.7</p>
-
</ol>
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</td>
 +
</tr></tbody>
 +
</table>
 +
<li>Note: The different concentrations are from different tubes.</p><p>2. The electrophoresis results are shown in Figure 2.</p><img src="https://static.igem.org/mediawiki/2014/4/49/T2.png"><p>Figure 2. A, C, and D the gel purification results and cleaved plasmids. B. the cleaved EP21.</p><h1 id="4" style="padding-top: 80px;
 +
  margin-top: -45px;">Week 4 8.11-8.17</h1><p>1. We did the liquid culture of BBa_R0077 and BBa_C0077.</p><p>2. We extracted the BBa_J37019, BBa_I9026 plasmids and then we cleaved both of them (BBa_J37019 with Spe I and Pst I; BBa_I9026 with Xba I and Pst I) and linked them with pSB1C3. Finally we tested the quality by transforming into E.coli.</p><p>3. We linked BBa_J37019 and BBa_I9026(LI1), BBa_R0077 and BBa_C0077 with pSB1C3.</p><p>4. We extracted BBa_I9026, BBa_J37019, BBa_C0077, and BBa_R0077.</p><p>5. We cleaved BBa_J37019 with E, S (D1, D2) or S, P (D3, D4) and BBa_I9026 plasmids with E, S, (D5, D6) and S, P (D7, D8) enzymes. Then we did the gel purification.</p><p>6. We linked the BBa_J37019 with BBa_I9026 with different types (named LI3).</p><p>7. We transformed LI3 into E.coli and extracted the plasmids to test the quality.</p><p>Results</p><table class="table table-striped"><caption>The concentration of plasmids</caption><thead><tr><td><p>Name</li>
 +
 
 +
</td><td><p>Concentration (ng/3&#956;l)</p>
 +
</td>
 +
</tr></thead><tbody><tr><td><p>BBa_I9026</p>
 +
</td><td><p>289.2/112.6</p>
 +
</td>
 +
</tr><tr><td><p>BBa_J37019</p>
 +
</td><td><p>193.2/40.7</p>
 +
</td>
 +
</tr><tr><td><p>BBa_C0077</p>
 +
</td><td><p>27.7/22.5/33.3</p>
 +
</td>
 +
</tr><tr><td><p>BBa_R0077</p>
 +
</td><td><p>177.8/179.8/200.3</p>
 +
</td>
 +
</tr></tbody>
 +
</table>
 +
<p>Note: The different concentrations are from different tubes.</p><p>2. The electrophoresis results are shown in Figure 3.</p><img src="https://static.igem.org/mediawiki/2014/thumb/a/a7/T3.png/471px-T3.png"><p>Figure A. the cleaved BBa_J37019 and BBa_I9026 plasmids. B. the cleaved linkage products. C and D is the gel purification of BBa_J37019 and BBa_I9026. E. the cleaved BBa_R0077 and BBa_C0077.</p><p>F. the linkage products.</p><h1 id="5" style="padding-top: 80px;
 +
  margin-top: -45px;">Week 5 8.18-8.24</h1><p>1. We linked the E11 and E12 with pSB1T3 by 3A assembly and E11 and E12 by traditional assembly.</p><p>2. We Amplified the LII3 which was tested by cleavage and electrophoresis.</p><p>3. We transformed the BBa_J37019, BBa_I9026, BBa_C0077, and L1T1.</p><p>4. We cultured the LIIF in liquid and transformed it.</p><p>5. We did the gel purification of BBa_J37019 and BBa_K747092.</p><p>Results</p><p>The electrophoresis results are shown in Figure 4.</p><img src="https://static.igem.org/mediawiki/2014/e/e7/T4.png"><p>Figure 4. A the gel purification results; B. the LII3 results.</p>
 +
 
</div></div>
</div></div>

Latest revision as of 03:59, 18 October 2014

The Notebook of

Transmitter

Since our team is sorted into 4 groups, our team is focusing on the construction of the Transmitter Cell. The whole work that we should do is to build 2 gene lines which lie in the transmitter cells.

In detail, we use 9 biobricks supplied by IGEM Competition totally which are RBS (BBa_B0030), DT (BBa_B0015), pLux (BBa_R0062), LuxR (BBa_C0062), LasI (BBa_K081016 and BBa_K081009), CinR (BBa_K0077), RhlR (BBa_C0171), and RhlI (BBa_C0051).

Week 1 7.20-7.26

1. We transformed the plasmids (BBa_B0030, BBa_B0015, BBa_R0062, BBa_K081016, BBa_K081009, BBa_K0077, BBa_C0171, BBa_C0051) into DH5α E.Coli to amplify these plasmid

We extracted the plasmids (mentioned above) and used electrophoresis to test the concentration and quality of our plasmids.

Results:

Name

Concentration (ng/3 μl)

BBa_R0062

53.3/ 43.5

BBa_K081016

107.9/ 176.7

BBa_B0030

28.2,/8.96

BBa_C0171

322.6/ 387.5

BBa_K0077

193.4,/143.9

BBa_K081009

64.4,/63.1

BBa_C0077

152.7/ 156

BBa_C0062

53.29/128.7

BBa_B0015

116.2/19.5

Note: The different concentrations are from different tubes.

Week 2 7.27-8.03

1. We transformed the BBa_C0062 and BBa_C0077 plasmids.

2. We extracted the BBa_J37019, BBa_I9026, BBa_K081005, BBa_I714075, BBa_K93600 and BBa_R0077 plasmids and determined the concentration of them by electrophoresis.

3. We cleaved the BBa_R0062, BBa_C0051, BBa_K0077 plasmids with EcoR I and Spe I enzyme and BBa_B0015 with Xba I and Pst I. Also, we prepared the pSB1A3 and pSB1K3 backbones with EcoR I and Pst I.

4. We cleaved the BBa_J37019 (Named E11) and BBa_R0077 (E21) with EcoR I and Spe I, BBa_I9026 (E12), BBa_K081016 (E22) and BBa_C0077 (E24) with Xba I and Pst I.

5. We linked the E11 and E12 with pSB1A3 (L11), the E21 and E22 with pSB1A3 (L21).

6. We transformed all the linked parts into E.coli.

7. We cleaved BBa_B0015 with Xba I and Pst I.

Results

The concentration of plasmids

Name

Concentration (ng/3μl)

BBa_J37019

400/403

BBa_I9026

247/140.6

BBa_R0077

134/161.2

BBa_K081005

51.2/27.6

BBa_I714075

95.7/37.2

BBa_K93600

41.6

L1

92.3/54.2

L2

88.4/60.4
  • Note: The different concentrations are from different tubes.

    2. The electrophoresis results are shown in Figure 1.

    Figure 1. The cleaved plasmids

    Week 3 8.04-8.10

    1. We linked the L1 and BBa_B0015 with pSB1T3 (named F1), L2 and BBa_I9026 with pSB1T3 (F2). Then we transformed them into E.coli to amplify them and we extracted the plasmids to test their quality.

    2. We linked E11 and E12 with pSB1T3 (named LA1), E21 and E22 with pSB1A3 (LA2).

    3. We cleaved the BBa_J37019 (Named E11) and BBa_R0077 (E21) with EcoR I and Spe I, BBa_I9026 (E12), BBa_K081016 (E22) and BBa_C0077 (E24) with Xba I and Pst I again and tested their qualities by electrophoresis and then we did the gel purification.

    4. We cleaved the BBa_R0077 with Spe I and Pst I (named EP21).

    5. We linked EP21 and E22 with 3 different backbones (pSB1T3, pSB1A3, and pSB1C3) which are tested by electrophoresis.

    Results:

    The concentration of plasmids and linkage product

    Name

    Concentration (ng/3μl)

    F11

    Failed

    F21

    failed

    E11

    8.53

    E12

    Failed

    E21

    24.9/7.5

    E22

    14/5.3

    E24

    18.1/17.7
  • Note: The different concentrations are from different tubes.

    2. The electrophoresis results are shown in Figure 2.

    Figure 2. A, C, and D the gel purification results and cleaved plasmids. B. the cleaved EP21.

    Week 4 8.11-8.17

    1. We did the liquid culture of BBa_R0077 and BBa_C0077.

    2. We extracted the BBa_J37019, BBa_I9026 plasmids and then we cleaved both of them (BBa_J37019 with Spe I and Pst I; BBa_I9026 with Xba I and Pst I) and linked them with pSB1C3. Finally we tested the quality by transforming into E.coli.

    3. We linked BBa_J37019 and BBa_I9026(LI1), BBa_R0077 and BBa_C0077 with pSB1C3.

    4. We extracted BBa_I9026, BBa_J37019, BBa_C0077, and BBa_R0077.

    5. We cleaved BBa_J37019 with E, S (D1, D2) or S, P (D3, D4) and BBa_I9026 plasmids with E, S, (D5, D6) and S, P (D7, D8) enzymes. Then we did the gel purification.

    6. We linked the BBa_J37019 with BBa_I9026 with different types (named LI3).

    7. We transformed LI3 into E.coli and extracted the plasmids to test the quality.

    Results

    The concentration of plasmids

    Name

    Concentration (ng/3μl)

    BBa_I9026

    289.2/112.6

    BBa_J37019

    193.2/40.7

    BBa_C0077

    27.7/22.5/33.3

    BBa_R0077

    177.8/179.8/200.3

    Note: The different concentrations are from different tubes.

    2. The electrophoresis results are shown in Figure 3.

    Figure A. the cleaved BBa_J37019 and BBa_I9026 plasmids. B. the cleaved linkage products. C and D is the gel purification of BBa_J37019 and BBa_I9026. E. the cleaved BBa_R0077 and BBa_C0077.

    F. the linkage products.

    Week 5 8.18-8.24

    1. We linked the E11 and E12 with pSB1T3 by 3A assembly and E11 and E12 by traditional assembly.

    2. We Amplified the LII3 which was tested by cleavage and electrophoresis.

    3. We transformed the BBa_J37019, BBa_I9026, BBa_C0077, and L1T1.

    4. We cultured the LIIF in liquid and transformed it.

    5. We did the gel purification of BBa_J37019 and BBa_K747092.

    Results

    The electrophoresis results are shown in Figure 4.

    Figure 4. A the gel purification results; B. the LII3 results.

    • Sichuan university

    Retrieved from "http://2014.igem.org/Team:SCU-China/Transmitter"