Team:TU Delft-Leiden/WetLab/landmine/cloning/yqjF

From 2014.igem.org

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Two final constructs are based on the yqjF promoter alone:
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<img src="https://static.igem.org/mediawiki/2014/9/96/TUDelft_Land_Mine_pF_Final_LandMines_History.png" width="100%" height="100%">
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<a href="http://parts.igem.org/Part:BBa_K1316003" style="text-decoration: none"" target="_blank"><font color="#0080FF" size="3">BBa_K1316003</font></a>
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and
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<a href="http://parts.igem.org/Part:BBa_K1316003" style="text-decoration: none"" target="_blank"><font color="#0080FF" size="3">BBa_K1316005</font></a>. For both of them the reporter gene mKate2 was placed behind the yqjF promoter. As BBa_K1316005 was built on bases of BBa_K1316003, a double transcriptional terminator was placed after the mKate2 gene. Otherwise, the RNA polymerase would continue transcribing and some unfinised transcripts of the N-genes could interfere with the normal expression of these genes. Therefore, mKate2 gene was first introduced in front of a Double terminator (
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<a href="http://parts.igem.org/Part:BBa_K823017" style="text-decoration: none"" target="_blank"><font color="#0080FF" size="3">BBa_K823017</font></a>  
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)
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Two final constructs are based on the yqjF promoter alone: <a href="http://parts.igem.org/Part:BBa_K1316003" style="text-decoration: none"" target="_blank"><font color="#0080FF" size="3">BBa_K1316003</font></a> and <a href="http://parts.igem.org/Part:BBa_K1316003" style="text-decoration: none"" target="_blank"><font color="#0080FF" size="3">BBa_K1316005</font></a>
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<img src="https://static.igem.org/mediawiki/2014/9/96/TUDelft_Land_Mine_pF_Final_LandMines_History.png" width="100%" height="100%">
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Revision as of 13:20, 30 September 2014

Landmine Module - Cloning - yqjF promoter

yqjF promoter

Two final constructs are based on the yqjF promoter alone: BBa_K1316003 and BBa_K1316005. For both of them the reporter gene mKate2 was placed behind the yqjF promoter. As BBa_K1316005 was built on bases of BBa_K1316003, a double transcriptional terminator was placed after the mKate2 gene. Otherwise, the RNA polymerase would continue transcribing and some unfinised transcripts of the N-genes could interfere with the normal expression of these genes. Therefore, mKate2 gene was first introduced in front of a Double terminator ( BBa_K823017 )

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