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| − | <h3>K1602044 - T7-B0034-enhanced yellow fluorescent protein-SH3-Ligand (T7-B0034-eYFP-SH3Lig)</h3>
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| − | <a href=” https://2015.igem.org/Team:TU_Darmstadt/Notebook/sec1/K1602041”title="Opens internal link in current window" class="internal link">K1602041</a> was digested with <em>Xba</em>I and <em>Pst</em>I. The construct was cloned into the vector pSB1A2 containing T7 promoter and transformed into competent <em>E. coli</em> Top 10 via heat shock. Colonies were screened by colony PCR (oligonucleotides VF2 and VR) (Figure 1). Positive clones were inoculated and the plasmids were extracted. Afterwards the construct was cloned into the vector pSB1C3 using <em>EcoR</em>I and <em>Pst</em>I. The pSB1C3 vector containing the coding sequence for T7-B0034-YFP-SH3Lig was used for protein expression in <em>E. coli</em> strain BL21.
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| − | <figure class="rightFig" style="width:30%">
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| − | <img src=" https://static.igem.org/mediawiki/2015/f/f0/Bild_3%3B_Colony_PCR_of_T7-B0034-YFP-Linker-SH3.png" width=100% height=100%>
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| − | <figcaption><br><b>Figure 1</b> Colony PCR of T7-B0034-YFP-SH3Lig (3-5). The size of the amplified product was around 1.1 kbp. DNA marker: 2-Log DNA Ladder. (NEB).</figcaption>
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| − | </figure>
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| − | </div></html>
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