Team:SDU-Denmark/labnotes6

From 2010.igem.org

(Difference between revisions)
(Lab notes (16/9 - 22/9))
(Lab notes (16/9 - 22/9))
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The gel picture shows that alle of the temperatures gave results.
The gel picture shows that alle of the temperatures gave results.
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==== Futher PCR on POT2 with NinaB (New Primers NO. 5) ====
 
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Date: 23/8<br>
 
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Done by: Marie & Tommy<br>
 
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Methods: PCR<br>
 
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protocos:CP.1.1[https://2010.igem.org/Team:SDU-Denmark/protocols#CP1.1]
 
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Notes:<br>
 
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NinB2fw and NinaB2rv was used.<br>
 
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PCR were run programed as:<br>
 
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<html>
 
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<head>
 
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  <meta content="text/html; charset=ISO-8859-1"
 
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http-equiv="content-type">
 
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  <title></title>
 
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</head>
 
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<body>
 
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<table style="text-align: left; width: 100%;" border="1"
 
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cellpadding="2" cellspacing="2">
 
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    <tr>
 
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      <td>PCR</td>
 
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      <td>Temp. (C)</td>
 
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      <td>Time (min)</td>
 
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    </tr>
 
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    <tr>
 
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      <td>Start</td>
 
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      <td>95</td>
 
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      <td>2</td>
 
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    </tr>
 
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    <tr>
 
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      <td>Denaturing</td>
 
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      <td>95</td>
 
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      <td>1</td>
 
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    </tr>
 
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    <tr>
 
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      <td>Anneling</td>
 
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      <td>67,9</td>
 
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      <td>1</td>
 
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    </tr>
 
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    <tr>
 
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      <td>Elongation</td>
 
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      <td>72</td>
 
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      <td>4</td>
 
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    </tr>
 
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    <tr>
 
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      <td>End</td>
 
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      <td>72</td>
 
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      <td>5</td>
 
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    </tr>
 
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    <tr>
 
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      <td>Hold</td>
 
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      <td>4</td>
 
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      <td>indef.</td>
 
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    </tr>
 
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</table>
 
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<br>
 
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</body>
 
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</html>
 
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<br>
 
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PCR product from gradient PCR (d. 20/8-10), tube no. 5, was used as template.<br>
 
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The other tubes were pooled.<br>
 
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=== PCR on POT2 with NinaB (New Primers) ===
 
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Start date: 24/8<br>
 
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Methods: Ligation, Competent cells, Transformation<br>
 
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Protocols: LG1.1[https://2010.igem.org/Team:SDU-Denmark/protocols#LG1.1], CC1.1[https://2010.igem.org/Team:SDU-Denmark/protocols#CC1.1], TR1.1[https://2010.igem.org/Team:SDU-Denmark/protocols#TR1.1]
 
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==== DNA purification from PCR ====
 
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Date: 20/8<br>
 
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Done by: Marie & Tommy<br>
 
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Methods: DNA purification from PCR<br>
 
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protocos:GFX purification from PCR - kit
 
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<br><br>
 
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One of the pooled tubes was eluted in 200µL, the others was eluted in 20µL<br>
 
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200µL nanodrop: 16,4 ng/µL<br>
 
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20µL nanodrop: 133,9ng/µL<br>
 
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==== Restriction Digest ====
 
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Date: 24/8<br>
 
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Done by: Marie & Tommy<br>
 
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Methods: Restriction Digest<br>
 
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protocos:RD1.1[https://2010.igem.org/Team:SDU-Denmark/protocols#RD1.1]
 
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Notes:<br>
 
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Restriction mixture:<br>
 
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<html>
 
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<head>
 
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  <meta content="text/html; charset=ISO-8859-1"
 
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http-equiv="content-type">
 
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  <title></title>
 
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</head>
 
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<body>
 
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<table style="text-align: left; width: 100%;" border="1"
 
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cellpadding="2" cellspacing="2">
 
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    <tr>
 
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      <td>38 µL</td>
 
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    </tr>
 
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    <tr>
 
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      <td>8 µL</td>
 
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    </tr>
 
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    <tr>
 
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      <td>4&nbsp;µL</td>
 
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    </tr>
 
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    <tr>
 
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      <td>4&nbsp;µL</td>
 
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    </tr>
 
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    <tr>
 
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      <td>30 µL</td>
 
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    </tr>
 
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</table>
 
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<br>
 
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</body>
 
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</html>
 
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Gel was run with uncut controles:<br>
 
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==== Gel purification ====
 
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Date: 24/8<br>
 
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Done by: Marie & Tommy<br>
 
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Methods: gel purifikation<br>
 
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protocos:GFX gel purifikation kit
 
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Notes:<br>
 
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Purifide products was Nanodroped:<br>
 
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NinaB 1: 4,5 ng/µL<br>
 
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NinaB 2: 1,15 ng/µL<br>
 
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NinaB 3: 7,74 ng/µL<br>
 
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PSB1C3: 25,66 ng/µL<br>
 
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Nina B pooled: 4,5 ng/µL<br>
 
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==== Ligation ====
 
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Date: 24/8<br>
 
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Done by: Marie & Tommy<br>
 
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Methods: Ligation<br>
 
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protocos:L1.3[https://2010.igem.org/Team:SDU-Denmark/protocols#LG1.3]
 
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Notes:<br>
 
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3 ligatons mixtures was made:<br>
 
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1:1 volumens 1 plasmid:5 insert
 
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1:3 volumens 1 plasmid:15 insert
 
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1:6 volumens 1 plasmid:30 insert
 

Revision as of 11:39, 1 September 2010