From 2014.igem.org

(Difference between revisions)

Latest revision as of 03:19, 18 October 2014

The Notebook of

Sensor

Since our team are sorted into 4 groups our target is constructing the Sensor cell in our system. According to our design, we need to construct two gene pathways. Consequently, we use the following parts: pLac (BBa_R0080), Promoter C and arabinose C operon (BBa_I13458), RBS (BBa_B0030), LuxI (BBa_C0061), double terminator (BBa_B0015), Constitutive promoter (BBa_J23100), CinI (BBa_C0076), pBAD (BBa_K206000), and LacI (BBa_C0012).

Week 1 7.12-7.19

1. We transformed the BBa_B0015, BBa_C0061, and BBa_B0030 plasmids into E.coli.

2. We extracted the plasmids and tested them by electrophoresis.

Results

The concentration of plasmids
Name	Concentration (ng/3μl)
BBa_B0015	118/59.5
BBa_B0030	23.7/23.2
BBa_C0061	260/161.9

Note: The different concentrations are from different tubes.

Week 2 7.20-7.26-

1. We transformed the BBa_K084012, BBa_I761014, BBa_K081005, BBa_J23100, BBa_K206000, BBa_R0080, BBa_C0076, BBa_C1002, and BBa_I13458 which are tested by cleavage and electrophoresis.

Results

The concentration of plasmids
Name	Concentration (ng/3μl)
BBa_K084012	26/35.4
BBa_I761014	49/68
BBa_K081005	32.2/22
BBa_J23100	120/75.7
BBa_K206000	58.7
BBa_R0080	Failed
BBa_C0076	98.6
BBa_C1002	85.7
BBa_I13458	496.6/242.6

Note: The different concentrations are from different tubes.

The electrophoresis results are shown in Figure 1.

Figure 1. The plasmids that has been cleaved by enzyme.

Week 3 7.27-8.03

1. We cleaved the BBa_K084012, BBa_C0012, BBa_I13458 with EcoR I and Spe I, BBa_I761014, and BBa_K206000 with Xba I and Pst I.

2. We amplified the BBa_K084012 and BBa_K081005 by transforming them into E.coli. And then we extracted the plasmids and tested them by electrophoresis.

3. We linked the BBa_K084012 and BBa_B0015; BBa_I13458 and BBa_K206000; BBa_K081005 and BBa_C1002 with pSB1A3.

Results

The concentration of plasmids
Name	Concentration (ng/3μl)
BBa_K084012	95.74/37.18
BBa_K081005	51.24/27.16

Note: The different concentrations are from different tubes.

2.

The electrophoresis results are shown in Figure 2.

Figure 2. The plasmids that have been cleaved by EcoR I and Spe I or Xba I and Pst I.

Week 4 8.04-8.10

1. We re-cleaved the BBa_K081005 for linkage (BBa_K081005 and BBa_C0012 with pSB1A3).

2. We transformed the linkage products into E.coli. Then we extracted the plasmids to test their qualities.

3. We transformed, extracted, and tested (BBa_K081005 and BBa_C0012 with pSB1A3).

4. We sent some of our linkage products to sequence them.

5. We extracted the BBa_B0015 and BBa_J0465

6. We cleaved the BBa_B0015 (E,X), BBa_K084012 PLUS BBa_B0015 (E, S), BBa_K084012 (E, S), BBa_K081005 (S,P), and BBa_C1002 (X,P) and we did the gel purification.

7. We amplified the BBa_I761014 by PCR.

Results

The concentration of plasmids
Name	Concentration
BBa_J0465	123.6/123.2
BBa_B0015	40/48/34

Note: The different concentrations are from different tubes.

The electrophoresis results are shown in Figure 3.

Figure 3. A and C show the plasmids that have been cleaved. B shows the PCR products.

Week 5 8.11-8.17

1. We linked the BBa_K081005 and BBa_C1002; BBa_I13458 PLUS BBa_K206000 and PCR products (Traditional Assembly); BBa_K084012 and BBa_B0015; BBa_K081005 and BBa_C1002 (3A Assembly) and transformed them.

2. We extracted the plasmids and did the linkage again (3A assembly).

3. We cleaved the BBa_K084012 (E, S) (Named Cut 1), BBa_B0015 (X, P) (Cut2), BBa_I13458 PLUS BBa_K206000 (E, S) (Cut3), PCR products (X, P) (Cut4), BBa_K81005 (E, S) (Cut5), BBa_C1002 (X, P) (Cut6).

We linked the Cut1 and Cut2 (Named Lia1); Cut3 and Cut4 (Lia 2 and 3); Cut5 and Cut6 (Lia 4).

Results

1.

The electrophoresis results are shown in Figure 4.

Figure 4. The parts that have been cleaved for linkage

Week 6 8.18-8.24

1. We cleaved the BBa_K081005 (E, S) and BBa_C1002 (X, P) plasmids.

2. We tested the lia 6-1-1 (X, P), lia 7-1-1 (X, P), lia 7-1-2 (X, P), lia 8-2-1 (E, S), and lia 8-2-2 (E, S) by cleavage and electrophoresis.

3. We did the gel purification for all the cleavage products.

4. We cleaved the BBa_K081005 (E, S), lia 6-1-4 (X, P), lia 6-1-1 (X, P), lia 6-1-2 (X, P), lia 6 -1-5 (X, P), lia 4-2-2 (E, S) and control group (E, S). Also, we prepared the linear backbones (pSB1T3 and pSB1C3) by cleavage.

5. We linked the CUT7 and CUT8 with pSB1T3 (Named NR 1), CUT3 and CUT4 with pSB1C3, pSB1T3, and pSB1K3, BBa_K081005 and CUT6 with pSB1T3 (NR 2).

6. We transformed the linkage products and extracted the BBa_I761014 and BBa_K084012 plasmids.

7. We cleaved the BBa_I761014 and BBa_C1002 with Xba I and Pst I. And we tested them by electrophoresis.

8. We amplified BBa_I761014 by PCR.

Results

The concentration of plasmids

Figure 5. A. gel purification result; B and C. the plasmids that have been cleaved by enzyme. D. PCR results.

Week 7 8.25-8.31

1. We tested the quality of our PCR products by electrophoresis.

2. We extracted the NR1-1, NR1-2, NR1-3, NR1-4, NR1-5, NR1-6, NR2-1, NR2-2, NR2-3, NR2-4, NR2-5, and NR2-6.

3. We tested BBa_B0015 (X, P), BBa_I13458 PLUS BBa_K206000 (E, S), BBa_C0012 (S, P), BBa_K084012 (X, P), NR1-1 (X, P), NR1-2 (X, P), NR2-1 (E, S), NR2-2 (E, S) by cleavage.

4. We cleaved NR2-3, NR2-5, NR2-6 with EcoR I and Spe I.

5. We linked the BBa_I13458 PLUS BBa_K20600 and our PCR products with pSB1K3 and pSB1C3.

6. We transformed the linkage products.

7. We tested the NR1-3, NR1-4 (E, S) and NR2-1/NR2-6 (X, P).

8. We amplified BBa_I761014 by PCR and did the PCR purification

9. We extracted NR3 and BBa_I761014 and tested them by electrophoresis and cleavage.

10. We linked BBa_I13458 PLUS BBa_K206000 and NP2 with pSB1T3 and pSB1C3.

11. We linked BBa_I13458 PLUS BBa_K206000 and BBa_I761014 with pSB1T3, BBa_0030 and BBa_C0076 with pSB1A3 and pSB1T3.

Results

The concentration of plasmids

Name	Concentration (ng/3 μl)
BBa_I761014	40
BBa_C0012	24

Name	Concentration (ng/3 μl)
NR1-1	95.5
NR1-2	127
NR1-3	105
NR1-4	128
NR1-5	128
NR1-6	110
NR2-1	112
NR2-2	138
NR2-3	135
NR2-4	128
NR2-5	102
NR2-6	Failed

The electrophoresis results are shown in Figure 6.

Figure 6. A. the results of cleaved plasmids and PCR products. B. and C. the results of linkage products.

Sichuan university

@@ Line 143: / Line 143: @@
 <ul class="nav nav-tabs nav-stacked" data-spy="affix" data-offset-top="125">
                 <li ><a href="#Top">Back to top</a></li>
-<li ><a href="#1">Week 1 8.21-8.24</a></li>
+<li ><a href="#1">Week 1</a></li>
-<li ><a href="#2">Week 2 8.25-8.31</a></li>
+<li ><a href="#2">Week 2</a></li>
+<li ><a href="#3">Week 3</a></li>
+<li ><a href="#4">Week 4</a></li>
+<li ><a href="#5">Week 5</a></li>
+<li ><a href="#6">Week 6</a></li>
+<li ><a href="#7">Week 7</a></li>
 </ul>	</div>
@@ Line 150: / Line 155: @@
-	<p>Since our team are sorted into 4 groups our target is constructing the Sensor cell in our system. According to our design, we need to construct two gene pathways. Consequently, we use the following parts: pLac (BBa_R0080), Promoter C and arabinose C operon (BBa_I13458), RBS (BBa_B0030), LuxI (BBa_C0061), double terminator (BBa_B0015), Constitutive promoter (BBa_J23100), CinI (BBa_C0076), pBAD (BBa_K206000), and LacI (BBa_C0012).</p><p>Week 1 7.12-7.19</p><p>1. We transformed the BBa_B0015, BBa_C0061, and BBa_B0030 plasmids into E.coli.</p><p>2. We extracted the plasmids and tested them by electrophoresis.</p><p>Results</p><table class="table table-striped"><caption>The concentration of plasmids</caption><thead><tr><td><p>Name</li>
+	<p>Since our team are sorted into 4 groups our target is constructing the Sensor cell in our system. According to our design, we need to construct two gene pathways. Consequently, we use the following parts: pLac (BBa_R0080), Promoter C and arabinose C operon (BBa_I13458), RBS (BBa_B0030), LuxI (BBa_C0061), double terminator (BBa_B0015), Constitutive promoter (BBa_J23100), CinI (BBa_C0076), pBAD (BBa_K206000), and LacI (BBa_C0012).</p><h1 id="1" style="padding-top: 80px;
+  margin-top: -45px;">Week 1 7.12-7.19</h1><p>1. We transformed the BBa_B0015, BBa_C0061, and BBa_B0030 plasmids into E.coli.</p><p>2. We extracted the plasmids and tested them by electrophoresis.</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>
@@ Line 166: / Line 172: @@
 </table>
 	<p>Note: The different concentrations are from different tubes.</p>
-<p>Week 2 7.20-7.26-</p>
+<h1 id="2"style="padding-top: 80px;
+  margin-top: -45px;">Week 2 7.20-7.26-</h1>
 <p>1. We transformed the BBa_K084012, BBa_I761014, BBa_K081005, BBa_J23100, BBa_K206000, BBa_R0080, BBa_C0076, BBa_C1002, and BBa_I13458 which are tested by cleavage and electrophoresis.</p><p>Results</p><table class="table table-striped"><caption>The concentration of plasmids</caption><thead><tr><td><p>Name</li>
@@ Line 203: / Line 210: @@
 	<img src="https://static.igem.org/mediawiki/2014/d/d8/Notebook_of_Sensor%281%291363.png">
   <p>Figure 1. The plasmids that has been cleaved by enzyme.</p>
-<p>Week 3 7.27-8.03</p><p>1. We cleaved the BBa_K084012, BBa_C0012, BBa_I13458 with EcoR I and Spe I, BBa_I761014, and BBa_K206000 with Xba I and Pst I.</p><p>2. We amplified the BBa_K084012 and BBa_K081005 by transforming them into E.coli. And then we extracted the plasmids and tested them by electrophoresis.</p><p>3. We linked the BBa_K084012 and BBa_B0015; BBa_I13458 and BBa_K206000; BBa_K081005 and BBa_C1002 with pSB1A3.</p><p>Results</p><table class="table table-striped"><caption>The concentration of plasmids</caption><thead><tr><td><p>Name</li>
+<h1 id="3" style="padding-top: 80px;
+  margin-top: -45px;">Week 3 7.27-8.03</h1><p>1. We cleaved the BBa_K084012, BBa_C0012, BBa_I13458 with EcoR I and Spe I, BBa_I761014, and BBa_K206000 with Xba I and Pst I.</p><p>2. We amplified the BBa_K084012 and BBa_K081005 by transforming them into E.coli. And then we extracted the plasmids and tested them by electrophoresis.</p><p>3. We linked the BBa_K084012 and BBa_B0015; BBa_I13458 and BBa_K206000; BBa_K081005 and BBa_C1002 with pSB1A3.</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>
@@ Line 215: / Line 223: @@
 </tr></tbody>
 </table><p>Note: The different concentrations are from different tubes.</p><p>2.<table><tr><td></td>
-</tr><tr><td></td><td><img width="337" height="124" src="Notebook of Sensor(1).files/Notebook of Sensor(1)2000.png"></td>
+</tr><tr><td></td><td></td>
 </tr>
 </table>
 <p>The electrophoresis results are shown in Figure 2.</p>
 	<img src="https://static.igem.org/mediawiki/2014/2/20/Notebook_of_Sensor%281%292000.png"
-<p>Figure 2. The plasmids that have been cleaved by EcoR I and Spe I or Xba I and Pst I.</p><p>Week 4 8.04-8.10</p><p>1. We re-cleaved the BBa_K081005 for linkage (BBa_K081005 and BBa_C0012 with pSB1A3).</p><p>2. We transformed the linkage products into E.coli. Then we extracted the plasmids to test their qualities.</p><p>3. We transformed, extracted, and tested (BBa_K081005 and BBa_C0012 with pSB1A3).</p><p>4. We sent some of our linkage products to sequence them.</p><p>5. We extracted the BBa_B0015 and BBa_J0465</p><p>6. We cleaved the BBa_B0015 (E,X), BBa_K084012 PLUS BBa_B0015 (E, S), BBa_K084012 (E, S), BBa_K081005 (S,P), and BBa_C1002 (X,P) and we did the gel purification.</p><p>7. We amplified the BBa_I761014 by PCR.</p><p>Results</p><table class="table table-striped"><caption>The concentration of plasmids</caption><thead><tr><td><p>Name</li>
+<p>Figure 2. The plasmids that have been cleaved by EcoR I and Spe I or Xba I and Pst I.</p><h1 id="4" style="padding-top: 80px;
+  margin-top: -45px;">Week 4 8.04-8.10</h1><p>1. We re-cleaved the BBa_K081005 for linkage (BBa_K081005 and BBa_C0012 with pSB1A3).</p><p>2. We transformed the linkage products into E.coli. Then we extracted the plasmids to test their qualities.</p><p>3. We transformed, extracted, and tested (BBa_K081005 and BBa_C0012 with pSB1A3).</p><p>4. We sent some of our linkage products to sequence them.</p><p>5. We extracted the BBa_B0015 and BBa_J0465</p><p>6. We cleaved the BBa_B0015 (E,X), BBa_K084012 PLUS BBa_B0015 (E, S), BBa_K084012 (E, S), BBa_K081005 (S,P), and BBa_C1002 (X,P) and we did the gel purification.</p><p>7. We amplified the BBa_I761014 by PCR.</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</p>
@@ Line 231: / Line 240: @@
 </td>
 </tr></tbody>
-</table><p>Note: The different concentrations are from different tubes.</p><p>2. <img width="52" height="37" src="Notebook of Sensor(1).files/Notebook of Sensor(1)2877.png"><img width="40" height="35" src="Notebook of Sensor(1).files/Notebook of Sensor(1)2878.png"><table><tr><td></td>
+</table><p>Note: The different concentrations are from different tubes.</p><p>
-</tr><tr><td></td><td><img width="208" height="290" src="Notebook of Sensor(1).files/Notebook of Sensor(1)2879.png"></td>
-</tr>
-</table>
-<img width="40" height="35" src="Notebook of Sensor(1).files/Notebook of Sensor(1)2880.png"><table><tr><td></td>
-</tr><tr><td></td><td><img width="285" height="292" src="Notebook of Sensor(1).files/Notebook of Sensor(1)2881.png"></td>
-</tr>
-</table><table><tr><td></td>
-</tr><tr><td></td><td><img width="259" height="259" src="Notebook of Sensor(1).files/Notebook of Sensor(1)2882.png"></td>
-</tr>
 </table>
 The electrophoresis results are shown in Figure 3.</p>
-	<li>Figure 3. A and C show the plasmids that have been cleaved. B shows the PCR products.</p><p>Week 5 8.11-8.17</p><p>1. We linked the BBa_K081005 and BBa_C1002; BBa_I13458 PLUS BBa_K206000 and PCR products (Traditional Assembly); BBa_K084012 and BBa_B0015; BBa_K081005 and BBa_C1002 (3A Assembly) and transformed them.</p><p>2. We extracted the plasmids and did the linkage again (3A assembly).</p><p>3. We cleaved the BBa_K084012 (E, S) (Named Cut 1), BBa_B0015 (X, P) (Cut2), BBa_I13458 PLUS BBa_K206000 (E, S) (Cut3), PCR products (X, P) (Cut4), BBa_K81005 (E, S) (Cut5), BBa_C1002 (X, P) (Cut6).</p><p>We linked the Cut1 and Cut2 (Named Lia1); Cut3 and Cut4 (Lia 2 and 3); Cut5 and Cut6 (Lia 4).</li><p><table><tr><td></td>
+	<img src="https://static.igem.org/mediawiki/2014/thumb/a/af/S3.png/580px-S3.png"
+<p>Figure 3. A and C show the plasmids that have been cleaved. B shows the PCR products.</p><h1 id="5" style="padding-top: 80px;
+  margin-top: -45px;">Week 5 8.11-8.17</h1><p>1. We linked the BBa_K081005 and BBa_C1002; BBa_I13458 PLUS BBa_K206000 and PCR products (Traditional Assembly); BBa_K084012 and BBa_B0015; BBa_K081005 and BBa_C1002 (3A Assembly) and transformed them.</p><p>2. We extracted the plasmids and did the linkage again (3A assembly).</p><p>3. We cleaved the BBa_K084012 (E, S) (Named Cut 1), BBa_B0015 (X, P) (Cut2), BBa_I13458 PLUS BBa_K206000 (E, S) (Cut3), PCR products (X, P) (Cut4), BBa_K81005 (E, S) (Cut5), BBa_C1002 (X, P) (Cut6).</p><p>We linked the Cut1 and Cut2 (Named Lia1); Cut3 and Cut4 (Lia 2 and 3); Cut5 and Cut6 (Lia 4).</li><p><table><tr><td></td>
-</tr><tr><td></td><td><img width="208" height="257" src="Notebook of Sensor(1).files/Notebook of Sensor(1)3596.png"></td>
+</tr><tr><td></td><td></td>
 </tr>
 </table>
 Results</p><p>1.<table><tr><td></td>
-</tr><tr><td></td><td><img width="287" height="329" src="Notebook of Sensor(1).files/Notebook of Sensor(1)3605.png"></td>
+</tr><tr><td></td><td></td>
 </tr>
 </table>
 The electrophoresis results are shown in Figure 4.</p>
-	<li>Figure 4. The parts that have been cleaved for linkage</p><p>Week 6 8.18-8.24</p><p>1. We cleaved the BBa_K081005 (E, S) and BBa_C1002 (X, P) plasmids.</p><p>2. We tested the lia 6-1-1 (X, P), lia 7-1-1 (X, P), lia 7-1-2 (X, P), lia 8-2-1 (E, S), and lia 8-2-2 (E, S) by cleavage and electrophoresis.</p><p>3. We did the gel purification for all the cleavage products.</p><p>4. We cleaved the BBa_K081005 (E, S), lia 6-1-4 (X, P), lia 6-1-1 (X, P), lia 6-1-2 (X, P), lia 6 -1-5 (X, P), lia 4-2-2 (E, S) and control group (E, S). Also, we prepared the linear backbones (pSB1T3 and pSB1C3) by cleavage.</p><p>5. We linked the CUT7 and CUT8 with pSB1T3 (Named NR 1), CUT3 and CUT4 with pSB1C3, pSB1T3, and pSB1K3, BBa_K081005 and CUT6 with pSB1T3 (NR 2).</p><p>6. We transformed the linkage products and extracted the BBa_I761014 and BBa_K084012 plasmids.</p><p>7. We cleaved the BBa_I761014 and BBa_C1002 with Xba I and Pst I. And we tested them by electrophoresis.</p><p>8. We amplified BBa_I761014 by PCR.</p><p>Results</p><p>The concentration of plasmids</p><table><tr><td><p>Name</li>
+	<img src="https://static.igem.org/mediawiki/2014/9/9b/S4.png"
+<p>Figure 4. The parts that have been cleaved for linkage</p><h1 id="6" style="padding-top: 80px;
+  margin-top: -45px;">Week 6 8.18-8.24</h1><p>1. We cleaved the BBa_K081005 (E, S) and BBa_C1002 (X, P) plasmids.</p><p>2. We tested the lia 6-1-1 (X, P), lia 7-1-1 (X, P), lia 7-1-2 (X, P), lia 8-2-1 (E, S), and lia 8-2-2 (E, S) by cleavage and electrophoresis.</p><p>3. We did the gel purification for all the cleavage products.</p><p>4. We cleaved the BBa_K081005 (E, S), lia 6-1-4 (X, P), lia 6-1-1 (X, P), lia 6-1-2 (X, P), lia 6 -1-5 (X, P), lia 4-2-2 (E, S) and control group (E, S). Also, we prepared the linear backbones (pSB1T3 and pSB1C3) by cleavage.</p><p>5. We linked the CUT7 and CUT8 with pSB1T3 (Named NR 1), CUT3 and CUT4 with pSB1C3, pSB1T3, and pSB1K3, BBa_K081005 and CUT6 with pSB1T3 (NR 2).</p><p>6. We transformed the linkage products and extracted the BBa_I761014 and BBa_K084012 plasmids.</p><p>7. We cleaved the BBa_I761014 and BBa_C1002 with Xba I and Pst I. And we tested them by electrophoresis.</p><p>8. We amplified BBa_I761014 by PCR.</p><p>Results</p><p>The concentration of plasmids</p><table><tr><td><p>Name</li>
 </td><td><p>Concentration (ng/3 &#956;l)</p>
@@ Line 264: / Line 268: @@
 </td>
 </tr>
-</table><p>2. <img width="26" height="31" src="Notebook of Sensor(1).files/Notebook of Sensor(1)4684.png"><img width="29" height="28" src="Notebook of Sensor(1).files/Notebook of Sensor(1)4685.png"><img width="26" height="31" src="Notebook of Sensor(1).files/Notebook of Sensor(1)4686.png"><img width="28" height="33" src="Notebook of Sensor(1).files/Notebook of Sensor(1)4687.png"><table><tr><td></td>
+<ing src="https://static.igem.org/mediawiki/2014/thumb/6/61/S5.png/570px-S5.png"
-</tr><tr><td></td><td><img width="242" height="350" src="Notebook of Sensor(1).files/Notebook of Sensor(1)4688.png"></td>
+<p>Figure 5. A. gel purification result; B and C. the plasmids that have been cleaved by enzyme. D. PCR results.</p>
-</tr>
+	<h1 id="7" style="padding-top: 80px;
-</table><table><tr><td></td>
+  margin-top: -45px;">Week 7 8.25-8.31</h1><p>1. We tested the quality of our PCR products by electrophoresis.</p><p>2. We extracted the NR1-1, NR1-2, NR1-3, NR1-4, NR1-5, NR1-6, NR2-1, NR2-2, NR2-3, NR2-4, NR2-5, and NR2-6.</p><p>3. We tested BBa_B0015 (X, P), BBa_I13458 PLUS BBa_K206000 (E, S), BBa_C0012 (S, P), BBa_K084012 (X, P), NR1-1 (X, P), NR1-2 (X, P), NR2-1 (E, S), NR2-2 (E, S) by cleavage.</p><p>4. We cleaved NR2-3, NR2-5, NR2-6 with EcoR I and Spe I.</p><p>5. We linked the BBa_I13458 PLUS BBa_K20600 and our PCR products with pSB1K3 and pSB1C3.</p><p>6. We transformed the linkage products.</p><p>7. We tested the NR1-3, NR1-4 (E, S) and NR2-1/NR2-6 (X, P).</p><p>8. We amplified BBa_I761014 by PCR and did the PCR purification</p><p>9. We extracted NR3 and BBa_I761014 and tested them by electrophoresis and cleavage.</p><p>10. We linked BBa_I13458 PLUS BBa_K206000 and NP2 with pSB1T3 and pSB1C3.</p><p>11. We linked BBa_I13458 PLUS BBa_K206000 and BBa_I761014 with pSB1T3, BBa_0030 and BBa_C0076 with pSB1A3 and pSB1T3.</p><p>Results</p><p>The concentration of plasmids</p><table><tr><td><p>Name</li>
-</tr><tr><td></td><td><img width="326" height="349" src="Notebook of Sensor(1).files/Notebook of Sensor(1)4689.png"></td>
-</tr>
-</table>
-The electrophoresis results are shown in Figure 5.</p><p><table><tr><td></td>
-</tr><tr><td></td><td><img width="210" height="314" src="Notebook of Sensor(1).files/Notebook of Sensor(1)4741.png"></td>
-</tr>
-</table><table><tr><td></td>
-</tr><tr><td></td><td><img width="317" height="307" src="Notebook of Sensor(1).files/Notebook of Sensor(1)4742.png"></td>
-</tr>
-</table>
-Figure 5. A. gel purification result; B and C. the plasmids that have been cleaved by enzyme. D. PCR results.</p>
-	<li>Week 7 8.25-8.31</p><p>1. We tested the quality of our PCR products by electrophoresis.</p><p>2. We extracted the NR1-1, NR1-2, NR1-3, NR1-4, NR1-5, NR1-6, NR2-1, NR2-2, NR2-3, NR2-4, NR2-5, and NR2-6.</p><p>3. We tested BBa_B0015 (X, P), BBa_I13458 PLUS BBa_K206000 (E, S), BBa_C0012 (S, P), BBa_K084012 (X, P), NR1-1 (X, P), NR1-2 (X, P), NR2-1 (E, S), NR2-2 (E, S) by cleavage.</p><p>4. We cleaved NR2-3, NR2-5, NR2-6 with EcoR I and Spe I.</p><p>5. We linked the BBa_I13458 PLUS BBa_K20600 and our PCR products with pSB1K3 and pSB1C3.</p><p>6. We transformed the linkage products.</p><p>7. We tested the NR1-3, NR1-4 (E, S) and NR2-1/NR2-6 (X, P).</p><p>8. We amplified BBa_I761014 by PCR and did the PCR purification</p><p>9. We extracted NR3 and BBa_I761014 and tested them by electrophoresis and cleavage.</p><p>10. We linked BBa_I13458 PLUS BBa_K206000 and NP2 with pSB1T3 and pSB1C3.</p><p>11. We linked BBa_I13458 PLUS BBa_K206000 and BBa_I761014 with pSB1T3, BBa_0030 and BBa_C0076 with pSB1A3 and pSB1T3.</p><p>Results</p><p>The concentration of plasmids</p><table><tr><td><p>Name</li>
 </td><td><p>Concentration (ng/3 &#956;l)</p>
@@ Line 322: / Line 314: @@
 </table>
 	<li></p><p>The electrophoresis results are shown in Figure 6.</p><p></li><p><table><tr><td></td>
+<img src="https://static.igem.org/mediawiki/2014/0/01/S6.png"
-</tr><tr><td></td><td><img width="262" height="165" src="Notebook of Sensor(1).files/Notebook of Sensor(1)6026.png"></td>
+<p>Figure 6. A. the results of cleaved plasmids and PCR products. B. and C. the results of linkage products.</p>
-</tr>
-</table><table><tr><td></td>
-</tr><tr><td></td><td><img width="236" height="163" src="Notebook of Sensor(1).files/Notebook of Sensor(1)6027.png"></td>
-</tr>
-</table>
-</p><p><img width="306" height="336" src="Notebook of Sensor(1).files/Notebook of Sensor(1)6029.png"></p><p>Figure 6. A. the results of cleaved plasmids and PCR products. B. and C. the results of linkage products.</p>
 </div></div>

Team:SCU-China/Sensor

From 2014.igem.org

Latest revision as of 03:19, 18 October 2014

Week 1 7.12-7.19

Week 2 7.20-7.26-

Week 3 7.27-8.03

Week 4 8.04-8.10

Week 5 8.11-8.17

Week 6 8.18-8.24

Week 7 8.25-8.31