Team:EPF Lausanne/Parts

From 2014.igem.org

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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486001</td>
     <td class="biobrick_name">BBa_K1486001</td>
-
     <td>CpxR + arabinose promoter</td>
+
     <td>Arabinose promoter + CpxR</td>
     <td>Transcription factor</td>
     <td>Transcription factor</td>
     <td> </td>
     <td> </td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486002</td>
     <td class="biobrick_name">BBa_K1486002</td>
-
     <td> Arabinose promoter + sfGFP CpxR [Nterm]</td>
+
     <td> Arabinose promoter + sfGFP-CpxR [Nterm]</td>
     <td>Expresses fused protein</td>
     <td>Expresses fused protein</td>
     <td>Test CpxR expression & Ara promoter</td>
     <td>Test CpxR expression & Ara promoter</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486005</td>
     <td class="biobrick_name">BBa_K1486005</td>
-
     <td>Ara promoter + CpxR sfGFP [Cterm]</td>
+
     <td>Arabinose promoter + sfGFP-CpxR [Cterm]</td>
     <td>Expresses fused protein</td>
     <td>Expresses fused protein</td>
     <td>Test CpxR expression & Ara promoter</td>
     <td>Test CpxR expression & Ara promoter</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486008</td>
     <td class="biobrick_name">BBa_K1486008</td>
-
     <td>CxpR & Split IFP1.4 [Cterm + Cterm]</td>
+
     <td>CpxR & Split IFP1.4 [Cterm + Cterm]</td>
     <td>Two CpxR CDS, each C terminus attached to a moiety of IFP</td>
     <td>Two CpxR CDS, each C terminus attached to a moiety of IFP</td>
     <td>Characterize CpxR dimerization</td>
     <td>Characterize CpxR dimerization</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486009</td>
     <td class="biobrick_name">BBa_K1486009</td>
-
     <td>CxpR & Split IFP1.4 [Nterm + Nterm]</td>
+
     <td>CpxR & Split IFP1.4 [Nterm + Nterm]</td>
     <td>Two CpxR CDS, each N terminus attached to a moiety of IFP</td>
     <td>Two CpxR CDS, each N terminus attached to a moiety of IFP</td>
     <td>Characterize CpxR dimerization</td>
     <td>Characterize CpxR dimerization</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486010</td>
     <td class="biobrick_name">BBa_K1486010</td>
-
     <td>CxpR & Split IFP1.4 [Nterm + Cterm]</td>
+
     <td>CpxR & Split IFP1.4 [Nterm + Cterm]</td>
     <td>Two CpxR CDS, each attached to a moiety of IFP</td>
     <td>Two CpxR CDS, each attached to a moiety of IFP</td>
     <td>Characterize CpxR dimerization</td>
     <td>Characterize CpxR dimerization</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486011</td>
     <td class="biobrick_name">BBa_K1486011</td>
-
     <td>CxpR & Split IFP1.4 [Cterm + Nterm]</td>
+
     <td>CpxR & Split IFP1.4 [Cterm + Nterm]</td>
     <td>Two CpxR CDS, each attached to a moiety of IFP</td>
     <td>Two CpxR CDS, each attached to a moiety of IFP</td>
     <td>Characterize CpxR dimerization</td>
     <td>Characterize CpxR dimerization</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486012</td>
     <td class="biobrick_name">BBa_K1486012</td>
-
     <td>CpxR-IFP[1] under pBAD]</td>
+
     <td>CpxR-IFP[1] under pBAD</td>
     <td>CpxR with the Nterm moiety of IFP attached at its C terminus</td>
     <td>CpxR with the Nterm moiety of IFP attached at its C terminus</td>
     <td>Intermediate & control</td>
     <td>Intermediate & control</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486015</td>
     <td class="biobrick_name">BBa_K1486015</td>
-
     <td>IFP[2] + CpxR</td>
+
     <td>IFP[2]-CpxR under pBAD</td>
     <td>CpxR with the Cterm moiety of IFP attached at its N terminus</td>
     <td>CpxR with the Cterm moiety of IFP attached at its N terminus</td>
     <td>Intermediate & control</td>
     <td>Intermediate & control</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486018</td>
     <td class="biobrick_name">BBa_K1486018</td>
-
     <td>PAra + fLuc[1] + fLuc[2]</td>
+
     <td>Arabinose promoter + fLuc[1] + fLuc[2]</td>
     <td>Split firefly luciferase under arabinose promoter</td>
     <td>Split firefly luciferase under arabinose promoter</td>
     <td>Control</td>
     <td>Control</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486021</td>
     <td class="biobrick_name">BBa_K1486021</td>
-
     <td>PAra + rLuc[1] + rLuc[2]</td>
+
     <td>Arabinose promoter + rLuc[1] + rLuc[2]</td>
     <td>Split renilla luciferase under arabinose promoter</td>
     <td>Split renilla luciferase under arabinose promoter</td>
     <td>Control</td>
     <td>Control</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486022</td>
     <td class="biobrick_name">BBa_K1486022</td>
-
     <td>rLuc</td>
+
     <td> Renilla Luciferase</td>
     <td>Full renilla luciferase</td>
     <td>Full renilla luciferase</td>
     <td>Control</td>
     <td>Control</td>
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<tr>
     <td class="biobrick_name">BBa_K1486023</td>
     <td class="biobrick_name">BBa_K1486023</td>
-
     <td>yeast sfGFP</td>
+
     <td>Yeast optimized superfolder GFP</td>
     <td>Yeast optimised superfolder GFP</td>
     <td>Yeast optimised superfolder GFP</td>
     <td>Reporter</td>
     <td>Reporter</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486024</td>
     <td class="biobrick_name">BBa_K1486024</td>
-
     <td>Kan</td>
+
     <td>Yeast kanamycin resistance</td>
     <td>Yeast kanamycin resistance</td>
     <td>Yeast kanamycin resistance</td>
     <td>Selection marker</td>
     <td>Selection marker</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486026</td>
     <td class="biobrick_name">BBa_K1486026</td>
-
     <td>sfGFP + ADH1+ Kan </td>
+
     <td>sfGFP + Kanamycin resistance for yeast </td>
-
     <td>tag</td>
+
     <td>Tag</td>
     <td>Control for the expression of Pbs2</td>
     <td>Control for the expression of Pbs2</td>
     <td>Yeast</td>
     <td>Yeast</td>
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<tr>
<tr>
     <td class="biobrick_name">BBa_K1486027</td>
     <td class="biobrick_name">BBa_K1486027</td>
-
     <td>rLuc + ADH1 + Kan</td>
+
     <td>R.reniformis luciferase + ADH1 terminator + Kanamycin resistance</td>
-
     <td>tag</td>
+
     <td>Tag</td>
     <td>Control for the expression of Pbs2 </td>
     <td>Control for the expression of Pbs2 </td>
     <td>Yeast</td>
     <td>Yeast</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486028</td>
     <td class="biobrick_name">BBa_K1486028</td>
-
     <td>Yeast sfGFP[1]</td>
+
     <td>Yeast optimized sfGFP N-terminus (1-214)</td>
     <td>Yeast optimized sfGFP N-terminus (1-214)</td>
     <td>Yeast optimized sfGFP N-terminus (1-214)</td>
     <td> </td>
     <td> </td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486029</td>
     <td class="biobrick_name">BBa_K1486029</td>
-
     <td>sfGFP[1] + ADH1 + kan</td>
+
     <td>Yeast Optimized sfGFP-N + ADH1 terminator + Kanamycin resistance</td>
     <td>N terminal moiety of split sfGFP</td>
     <td>N terminal moiety of split sfGFP</td>
     <td>Complementation Assay </td>
     <td>Complementation Assay </td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486030</td>
     <td class="biobrick_name">BBa_K1486030</td>
-
     <td>rLuc[1] + ADH1 + kan</td>
+
     <td>rLucN + ADH1 terminator + Kanamycin resistance</td>
     <td>N terminal moiety of split rLuc</td>
     <td>N terminal moiety of split rLuc</td>
     <td>Complementation Assay  </td>
     <td>Complementation Assay  </td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486031</td>
     <td class="biobrick_name">BBa_K1486031</td>
-
     <td>Ura3 cassette</td>
+
     <td>CaUra3 selection marker</td>
     <td>selection marker</td>
     <td>selection marker</td>
     <td>Confer resistance to Uracil-deprived medium</td>
     <td>Confer resistance to Uracil-deprived medium</td>
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     <td class="biobrick_name">BBa_K1486032</td>
     <td class="biobrick_name">BBa_K1486032</td>
     <td>sfGFP + ADH1 terminator + Ura3 cassette</td>
     <td>sfGFP + ADH1 terminator + Ura3 cassette</td>
-
     <td>tag</td>
+
     <td>Tag</td>
     <td>Control for the expression of hog1</td>
     <td>Control for the expression of hog1</td>
     <td>Yeast</td>
     <td>Yeast</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486033</td>
     <td class="biobrick_name">BBa_K1486033</td>
-
     <td>rLuc + ADH1 + Ura</td>
+
     <td>sfGFP + ADH1 terminator + Ura3 cassette</td>
-
     <td>tag</td>
+
     <td>Tag</td>
     <td>Control for the expression of hog1</td>
     <td>Control for the expression of hog1</td>
     <td>Yeast</td>
     <td>Yeast</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486034</td>
     <td class="biobrick_name">BBa_K1486034</td>
-
     <td>yeast sfGFP[2]</td>
+
     <td>Yeast optimized superfolder GFP C-terminus (215-238)</td>
     <td>Yeast optimized superfolder GFP C-terminus (215-238)</td>
     <td>Yeast optimized superfolder GFP C-terminus (215-238)</td>
     <td> </td>
     <td> </td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486035</td>
     <td class="biobrick_name">BBa_K1486035</td>
-
     <td>yeast sfGFP[2]+ ADH1 + Ura</td>
+
     <td>Yeast Optimized sfGFP-C + ADH1 terminator + CaUra3 Cassette</td>
     <td>C terminal moiety of split sfGFP</td>
     <td>C terminal moiety of split sfGFP</td>
     <td>Complementation Assay </td>
     <td>Complementation Assay </td>
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<tr>
<tr>
     <td class="biobrick_name">BBa_K1486036</td>
     <td class="biobrick_name">BBa_K1486036</td>
-
     <td>rLuc[2] + ADH1 + Ura</td>
+
     <td>rLucC + ADH1 terminator + CaUra3 cassette</td>
     <td>C terminal moiety of split rLuc</td>
     <td>C terminal moiety of split rLuc</td>
     <td>Complementation Assay </td>
     <td>Complementation Assay </td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486038</td>
     <td class="biobrick_name">BBa_K1486038</td>
-
     <td>sfGFP[1]</td>
+
     <td>sfGFPN</td>
     <td>N terminus moiety of split superfolder GFP</td>
     <td>N terminus moiety of split superfolder GFP</td>
     <td> </td>
     <td> </td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486039</td>
     <td class="biobrick_name">BBa_K1486039</td>
-
     <td>sfGFP[2]</td>
+
     <td>sfGFPC</td>
     <td>C terminus moiety of split superfolder GFP</td>
     <td>C terminus moiety of split superfolder GFP</td>
     <td> </td>
     <td> </td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486040</td>
     <td class="biobrick_name">BBa_K1486040</td>
-
     <td>sfGFP[1] + CpxR</td>
+
     <td>sfGFPN + CpxR</td>
     <td>N terminus moiety of split sfGFP attached to CpxR</td>
     <td>N terminus moiety of split sfGFP attached to CpxR</td>
     <td> </td>
     <td> </td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486041</td>
     <td class="biobrick_name">BBa_K1486041</td>
-
     <td>sfGFP[2] + CpxR</td>
+
     <td>sfGFPC + CpxR</td>
     <td>C terminus moiety of split sfGFP attached to CpxR</td>
     <td>C terminus moiety of split sfGFP attached to CpxR</td>
     <td> </td>
     <td> </td>
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   <tr>
     <td class="biobrick_name">BBa_K1486042</td>
     <td class="biobrick_name">BBa_K1486042</td>
-
     <td>LZip</td>
+
     <td>Leucine Zipper</td>
     <td>Monomer of leucine zipper TF</td>
     <td>Monomer of leucine zipper TF</td>
     <td> </td>
     <td> </td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486043</td>
     <td class="biobrick_name">BBa_K1486043</td>
-
     <td>LZip + split rLuc</td>
+
     <td>Leucine Zipper + split rLuc</td>
     <td>Two Leucine Zipper monomers, each attached to a different split rLuc moiety</td>
     <td>Two Leucine Zipper monomers, each attached to a different split rLuc moiety</td>
     <td>Control for split rLuc assays</td>
     <td>Control for split rLuc assays</td>
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   <tr>
     <td class="biobrick_name">BBa_K1486044</td>
     <td class="biobrick_name">BBa_K1486044</td>
-
     <td>mut IFP[1]</td>
+
     <td>IFP[1] Mutated</td>
     <td>Biobrick-compatible IFP[1]</td>
     <td>Biobrick-compatible IFP[1]</td>
     <td> </td>
     <td> </td>
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   <tr>
     <td class="biobrick_name">BBa_K1486045</td>
     <td class="biobrick_name">BBa_K1486045</td>
-
     <td>mut IFP[2]</td>
+
     <td>IFP[2] Mutated</td>
     <td>Biobrick-compatible IFP[2]</td>
     <td>Biobrick-compatible IFP[2]</td>
     <td> </td>
     <td> </td>
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   <tr>
     <td class="biobrick_name">BBa_K1486053</td>
     <td class="biobrick_name">BBa_K1486053</td>
-
     <td>Linker</td>
+
     <td>10 aa linker</td>
     <td>10 amino-acid linker</td>
     <td>10 amino-acid linker</td>
     <td>Attach CheY/Z to split luciferases</td>
     <td>Attach CheY/Z to split luciferases</td>
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     <td class="biobrick_name">BBa_K1486054</td>
     <td class="biobrick_name">BBa_K1486054</td>
-
     <td>CheY/CheZ rLuc</td>
+
     <td>CheY/CheZ + split rLuc</td>
     <td>CheY and CheZ, each attached to a moiety of split renilla luciferase</td>
     <td>CheY and CheZ, each attached to a moiety of split renilla luciferase</td>
     <td>Positive control for the split rLuc</td>
     <td>Positive control for the split rLuc</td>
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   <tr>
     <td class="biobrick_name">BBa_K1486055</td>
     <td class="biobrick_name">BBa_K1486055</td>
-
     <td>CheY/CheZ fLuc</td>
+
     <td>CheY/CheZ + split fLuc</td>
     <td>CheY and CheZ, each attached to a moiety of split firefly luciferase</td>
     <td>CheY and CheZ, each attached to a moiety of split firefly luciferase</td>
     <td>Positive control for the split fLuc</td>
     <td>Positive control for the split fLuc</td>
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   <tr>
   <tr>
     <td class="biobrick_name">BBa_K1486056</td>
     <td class="biobrick_name">BBa_K1486056</td>
-
     <td>CxpR & Split mut IFP1.4 [Cterm + Cterm]</td>
+
     <td>CpxR & Split IFP1.4 [Cterm + Cterm][2]</td>
     <td>Two CpxR CDS, each C terminus attached to a moiety of the biobrick-compatible IFP</td>
     <td>Two CpxR CDS, each C terminus attached to a moiety of the biobrick-compatible IFP</td>
     <td>Characterize CpxR dimerization</td>
     <td>Characterize CpxR dimerization</td>
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<p class="lead">When designing the chips, the team took into account the future users and the current iGEM classification of parts. We considered it best to construct our chips as composite microfluidic parts, so their sub-parts could be used and combined in multiple ways. The flow and control layers can be separated and reused, as well as all the basic structures (chamber + connecting channel), nodes, array parts,...</p>
<p class="lead">When designing the chips, the team took into account the future users and the current iGEM classification of parts. We considered it best to construct our chips as composite microfluidic parts, so their sub-parts could be used and combined in multiple ways. The flow and control layers can be separated and reused, as well as all the basic structures (chamber + connecting channel), nodes, array parts,...</p>
-
 
+
<p>By clicking on each of the designs' name, you can download the original files.</p>
<!-- send all lines here: https://2014.igem.org/Team:EPF_Lausanne/Microfluidics/Designing -->
<!-- send all lines here: https://2014.igem.org/Team:EPF_Lausanne/Microfluidics/Designing -->
<table class="table table-striped table-hover" id="chips_list">
<table class="table table-striped table-hover" id="chips_list">

Latest revision as of 01:45, 18 October 2014

PARTS


DNA parts submitted by the 2014 EPFL iGEM team

Our team submitted a total of 55 Biobricks (part 51 does not exist).

In addition, 4 microfluidic designs have also been submitted to the registry.

Biobrick What it is Function Why do we use it? Group
BBa_K1486000 CpxR coding sequence Transcription factor To make most of our biobricks! Bacteria
BBa_K1486001 Arabinose promoter + CpxR Transcription factor Bacteria
BBa_K1486002 Arabinose promoter + sfGFP-CpxR [Nterm] Expresses fused protein Test CpxR expression & Ara promoter Bacteria
BBa_K1486003 Flexible linker 2x (GGGS) Attaches two proteins together Bacteria
BBa_K1486004 Flexible linker 2x (GGGGS) Attaches two proteins together Bacteria
BBa_K1486005 Arabinose promoter + sfGFP-CpxR [Cterm] Expresses fused protein Test CpxR expression & Ara promoter Bacteria
BBa_K1486006 IFP[1] N terminus of split IFP Bacteria
BBa_K1486007 IFP[2] C terminus of split IFP Bacteria
BBa_K1486008 CpxR & Split IFP1.4 [Cterm + Cterm] Two CpxR CDS, each C terminus attached to a moiety of IFP Characterize CpxR dimerization Bacteria
BBa_K1486009 CpxR & Split IFP1.4 [Nterm + Nterm] Two CpxR CDS, each N terminus attached to a moiety of IFP Characterize CpxR dimerization Bacteria
BBa_K1486010 CpxR & Split IFP1.4 [Nterm + Cterm] Two CpxR CDS, each attached to a moiety of IFP Characterize CpxR dimerization Bacteria
BBa_K1486011 CpxR & Split IFP1.4 [Cterm + Nterm] Two CpxR CDS, each attached to a moiety of IFP Characterize CpxR dimerization Bacteria
BBa_K1486012 CpxR-IFP[1] under pBAD CpxR with the Nterm moiety of IFP attached at its C terminus Intermediate & control Bacteria
BBa_K1486013 CpxR-IFP[2] under pBAD CpxR with the Cterm moiety of IFP attached at its C terminus Intermediate & control Bacteria
BBa_K1486014 IFP[1]-CpxR under pBAD CpxR with the Nterm moiety of IFP attached at its N terminus Intermediate & control Bacteria
BBa_K1486015 IFP[2]-CpxR under pBAD CpxR with the Cterm moiety of IFP attached at its N terminus Intermediate & control Bacteria
BBa_K1486016 fLuc[1] N terminus moiety of the firefly luciferase Bacteria
BBa_K1486017 fLuc[2] C terminus moiety of the firefly luciferase Bacteria
BBa_K1486018 Arabinose promoter + fLuc[1] + fLuc[2] Split firefly luciferase under arabinose promoter Control Bacteria
BBa_K1486019 rLuc[1] C terminus moiety of the renilla luciferase Bacteria
BBa_K1486020 rLuc[2] N terminus moiety of the renilla luciferase Bacteria
BBa_K1486021 Arabinose promoter + rLuc[1] + rLuc[2] Split renilla luciferase under arabinose promoter Control Bacteria
BBa_K1486022 Renilla Luciferase Full renilla luciferase Control Bacteria
BBa_K1486023 Yeast optimized superfolder GFP Yeast optimised superfolder GFP Reporter Yeast
BBa_K1486024 Yeast kanamycin resistance Yeast kanamycin resistance Selection marker Yeast
BBa_K1486025 ADH1 terminator Terminator Abortion of the transcription at the end of our DNA sequences Yeast
BBa_K1486026 sfGFP + Kanamycin resistance for yeast Tag Control for the expression of Pbs2 Yeast
BBa_K1486027 R.reniformis luciferase + ADH1 terminator + Kanamycin resistance Tag Control for the expression of Pbs2 Yeast
BBa_K1486028 Yeast optimized sfGFP N-terminus (1-214) Yeast optimized sfGFP N-terminus (1-214) Yeast
BBa_K1486029 Yeast Optimized sfGFP-N + ADH1 terminator + Kanamycin resistance N terminal moiety of split sfGFP Complementation Assay Yeast
BBa_K1486030 rLucN + ADH1 terminator + Kanamycin resistance N terminal moiety of split rLuc Complementation Assay Yeast
BBa_K1486031 CaUra3 selection marker selection marker Confer resistance to Uracil-deprived medium Yeast
BBa_K1486032 sfGFP + ADH1 terminator + Ura3 cassette Tag Control for the expression of hog1 Yeast
BBa_K1486033 sfGFP + ADH1 terminator + Ura3 cassette Tag Control for the expression of hog1 Yeast
BBa_K1486034 Yeast optimized superfolder GFP C-terminus (215-238) Yeast optimized superfolder GFP C-terminus (215-238) Yeast
BBa_K1486035 Yeast Optimized sfGFP-C + ADH1 terminator + CaUra3 Cassette C terminal moiety of split sfGFP Complementation Assay Yeast
BBa_K1486036 rLucC + ADH1 terminator + CaUra3 cassette C terminal moiety of split rLuc Complementation Assay Yeast
BBa_K1486037 13 amino acids linker [GGGS GGGGS GGGS] linker Attach Pbs2 or Hog1 to our different tags and splits Yeast
BBa_K1486038 sfGFPN N terminus moiety of split superfolder GFP Bacteria
BBa_K1486039 sfGFPC C terminus moiety of split superfolder GFP Bacteria
BBa_K1486040 sfGFPN + CpxR N terminus moiety of split sfGFP attached to CpxR Bacteria
BBa_K1486041 sfGFPC + CpxR C terminus moiety of split sfGFP attached to CpxR Bacteria
BBa_K1486042 Leucine Zipper Monomer of leucine zipper TF Bacteria
BBa_K1486043 Leucine Zipper + split rLuc Two Leucine Zipper monomers, each attached to a different split rLuc moiety Control for split rLuc assays Bacteria
BBa_K1486044 IFP[1] Mutated Biobrick-compatible IFP[1] Bacteria
BBa_K1486045 IFP[2] Mutated Biobrick-compatible IFP[2] Bacteria
BBa_K1486046 CpxR promoter FW CpxR binding-region in forward direction Bacteria
BBa_K1486047 CpxR promoter RV CpxR binding-region in reverse direction Bacteria
BBa_K1486048 CpxR reporter Calgary's CpxR reporter repaired (sequence was missing) To see when CpxR is active Bacteria
BBa_K1486049 CpxR promoter FW + RFP Reporter of CpxR Test the direction of the complete CpxR promoter Bacteria
BBa_K1486050 CpxR promoter RV + RFP Reporter of CpxR Test the direction of the complete CpxR promoter Bacteria
BBa_K1486052 Spacer 40 bases placed between constructs Separate two constructs in the same plasmid Bacteria
BBa_K1486053 10 aa linker 10 amino-acid linker Attach CheY/Z to split luciferases Bacteria
BBa_K1486054 CheY/CheZ + split rLuc CheY and CheZ, each attached to a moiety of split renilla luciferase Positive control for the split rLuc Bacteria
BBa_K1486055 CheY/CheZ + split fLuc CheY and CheZ, each attached to a moiety of split firefly luciferase Positive control for the split fLuc Bacteria
BBa_K1486056 CpxR & Split IFP1.4 [Cterm + Cterm][2] Two CpxR CDS, each C terminus attached to a moiety of the biobrick-compatible IFP Characterize CpxR dimerization Bacteria


Microfluidics parts (chips created)

Our team designed and made 4 microfluidic chips. At the beginning, we also used the MITOMI chip.

When designing the chips, the team took into account the future users and the current iGEM classification of parts. We considered it best to construct our chips as composite microfluidic parts, so their sub-parts could be used and combined in multiple ways. The flow and control layers can be separated and reused, as well as all the basic structures (chamber + connecting channel), nodes, array parts,...

By clicking on each of the designs' name, you can download the original files.

Name Main Function
SmashColi To be able to separate the chip in 4 different compartments and apply 4 different pressures on each row of chambers.
The BioPad A large and simple microfluidic chip containing 6400 chambers in which the cells are contained in. Each chamber acts as a pixel for the BioPad project.
CleanColi As a result of our Safety page, we decided to create a chip that is able to seal the bacteria in the chip, preventing them to leave the chip.
FilterColi To successfully immerse cells in a certain solution, this chip was designed to flow in the new medium in the chambers instead of doing it by diffusion.


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