Team:Goettingen/week8-3

From 2012.igem.org

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<b>V06_21_1 Preparative digest of promoter_TAR_QC constructs and pSB1C3</b><br>
<b>V06_21_1 Preparative digest of promoter_TAR_QC constructs and pSB1C3</b><br>
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<li>Experiment: <br>All 8 promoter constructs + TAR_QC in pUC18 and the BioBrick vector pSB1C3 were digested according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol.</a></li>
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<li>Experiment: <br>All 8 promoter constructs + TAR_QC in J61002 and the BioBrick vector pSB1C3 were digested with <i>Xba</i>I and <i>Pst</i>I according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol. </a></li>
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<li>Observations and results: <br>The transformation of DH10B with pSB1C3 (see V06_18) worked well.
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<li>Observations and results: <br>The transformation of DH10B with pSB1C3 (see V06_18) worked well. pSB1C3 contained RFP which is now cut out.
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<h2><b>V06_22 </b></h2><br>
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<b>Isolation of vector backbone pSB1C3 from BioBrick distribution kit</b><br>
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<li>Experiment: <br>The vector pSB1C3 is used as the standard vector for BioBricks in this year's iGEM competition. We transformed <i>E. coli</i> DH10B with pSB1C3 according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a> and streaked these out on Chloramphenicol (CM) plates.</li>
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Revision as of 11:49, 17 September 2012