Team:Goettingen/week6-3

From 2012.igem.org

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<h2><b>V06_08 </b></h2><br>
<h2><b>V06_08 </b></h2><br>
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<b>V06_08-1 Preparative double digest of pUC18_TAR_QC</b><br>
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<b>V06_08_1 Preparative double digest of pUC18_TAR_QC</b><br>
<ul>
<ul>
<li>Experiment: <br>Digest was performd with <i>Xba</i>I and <i>Pst</i>I (according to BioBrick standard) according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>. A gelelectrophoresis of the digest was performed which showed the expected bands at 2662 bp and 1680 bp. The insert TAR_QC (1680 bp) was cut from the gel and a gel extraction was performed as described before. Stored at -20 °C.
<li>Experiment: <br>Digest was performd with <i>Xba</i>I and <i>Pst</i>I (according to BioBrick standard) according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>. A gelelectrophoresis of the digest was performed which showed the expected bands at 2662 bp and 1680 bp. The insert TAR_QC (1680 bp) was cut from the gel and a gel extraction was performed as described before. Stored at -20 °C.
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</ul>
</ul>
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<br>
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<b>V06_08-2 Sequencing of pUC18_TAR_QC</b><br>
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<b>V06_08_2 Sequencing of pUC18_TAR_QC</b><br>
<ul>
<ul>
<li>Experiment: <br>Sequencing reactions were done by Prof. Daniels Laboratory (University of Göttingen), Göttingen Genomics Lab and set up according to their <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>. Primers used: pUC18_M13 for, pUC18_M13 rev, pUC18_TAR_Seqfor01, pUC18_TAR_Seqfor02. Dilutions 100 &mu;M, 10 &mu;M, 5 pmol.
<li>Experiment: <br>Sequencing reactions were done by Prof. Daniels Laboratory (University of Göttingen), Göttingen Genomics Lab and set up according to their <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>. Primers used: pUC18_M13 for, pUC18_M13 rev, pUC18_TAR_Seqfor01, pUC18_TAR_Seqfor02. Dilutions 100 &mu;M, 10 &mu;M, 5 pmol.

Revision as of 10:32, 15 September 2012