Difference between revisions of "Team:TU Darmstadt/Notebook/sec1/K1602024"
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− | Competent <em>E. coli </em>Top 10 cells were retransformed via heat shock with pSB1C3 harbouring <em> GFP</em> provided by the iGEM Registry. The plasmids were extracted and used as templates for a PCR with oligonucleotides 42 and VR. The PCR product was verified by gel electrophoresis (Figure 1) and digested with <em> Dpn</em>I. The purified product was digested with <em>EcoR</em>I and <em>Pst</em>I and ligated into pSB1C3. Competent <em>E. coli</em> Top 10 cells were transformed via heat shock and colonies were screened by colony PCR with oligonucleotides VF2 and VR (Figure 2). | + | Competent <em>E. coli </em>Top 10 cells were retransformed via heat shock with pSB1C3 harbouring <em> GFP</em> provided by the iGEM Registry <a href=" http://parts.igem.org/Part:BBa_E0040 " title="Opens internal link in current window" class="internal link">BBa_E0040</a>. The plasmids were extracted and used as templates for a PCR with oligonucleotides 42 and VR. The PCR product was verified by gel electrophoresis (Figure 1) and digested with <em> Dpn</em>I. The purified product was digested with <em>EcoR</em>I and <em>Pst</em>I and ligated into pSB1C3. Competent <em>E. coli</em> Top 10 cells were transformed via heat shock and colonies were screened by colony PCR with oligonucleotides VF2 and VR (Figure 2). |
<figure class="leftFig" style="width:30%"> | <figure class="leftFig" style="width:30%"> | ||
<img src="https://static.igem.org/mediawiki/2015/8/83/Figure_1-_Standard_PCR_of_Prefix-His-Tag-GFP.png" width=100% height=100%> | <img src="https://static.igem.org/mediawiki/2015/8/83/Figure_1-_Standard_PCR_of_Prefix-His-Tag-GFP.png" width=100% height=100%> |
Revision as of 19:56, 16 September 2015
K1602024 - HistidinTag-Green fluorescent protein (His-GFP)
Competent E. coli Top 10 cells were retransformed via heat shock with pSB1C3 harbouring GFP provided by the iGEM Registry BBa_E0040. The plasmids were extracted and used as templates for a PCR with oligonucleotides 42 and VR. The PCR product was verified by gel electrophoresis (Figure 1) and digested with DpnI. The purified product was digested with EcoRI and PstI and ligated into pSB1C3. Competent E. coli Top 10 cells were transformed via heat shock and colonies were screened by colony PCR with oligonucleotides VF2 and VR (Figure 2).