Zhaowenxue (Talk | contribs) |
Zhaowenxue (Talk | contribs) |
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<a data-toggle="collapse" data-parent="#accordion" href="#collapseOne"> | <a data-toggle="collapse" data-parent="#accordion" href="#collapseOne"> | ||
− | + | Week 5 | |
</a> | </a> | ||
</h4> | </h4> | ||
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<div id="collapseOne" class="panel-collapse collapse"> | <div id="collapseOne" class="panel-collapse collapse"> | ||
<div class="panel-body"> | <div class="panel-body"> | ||
− | + | Find promoters with various strength in the light of transcriptom references. Take the sequence from the upstream of a specific gene. | |
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</div> | </div> | ||
</div> | </div> | ||
</div> | </div> | ||
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<div class="panel panel-default"> | <div class="panel panel-default"> | ||
<div class="panel-heading"> | <div class="panel-heading"> | ||
<h4 class="panel-title"> | <h4 class="panel-title"> | ||
<a data-toggle="collapse" data-parent="#accordion" href="#collapseTwo"> | <a data-toggle="collapse" data-parent="#accordion" href="#collapseTwo"> | ||
− | + | Week 6 | |
</a> | </a> | ||
</h4> | </h4> | ||
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<div id="collapseTwo" class="panel-collapse collapse"> | <div id="collapseTwo" class="panel-collapse collapse"> | ||
<div class="panel-body"> | <div class="panel-body"> | ||
− | + | design the PAGE-purified oligonucleotides used to amplify the chloramphenicol and add homology arm for rencombination. | |
− | + | ||
</div> | </div> | ||
</div> | </div> | ||
</div> | </div> | ||
− | |||
<div class="panel panel-default"> | <div class="panel panel-default"> | ||
<div class="panel-heading"> | <div class="panel-heading"> | ||
<h4 class="panel-title"> | <h4 class="panel-title"> | ||
− | <a data-toggle="collapse" data-parent="#accordion" | + | <a data-toggle="collapse" data-parent="#accordion" href="#collapseThree"> |
− | + | Week 7 & 8 | |
</a> | </a> | ||
</h4> | </h4> | ||
</div> | </div> | ||
− | <div id=" | + | <div id="collapseThree" class="panel-collapse collapse"> |
<div class="panel-body"> | <div class="panel-body"> | ||
− | + | amplify the chloramphnicol and promoter segment and add vector homology arms via series PCR. Purify the PCR products using the TianGen PCR Purification Kit and elute into 30ul of autoclaved ddH2O. Quantify the elution using a NanoDrop UV spectrophotometer, store them at 4℃ | |
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</div> | </div> | ||
</div> | </div> | ||
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<div class="panel-heading"> | <div class="panel-heading"> | ||
<h4 class="panel-title"> | <h4 class="panel-title"> | ||
− | <a data-toggle="collapse" data-parent="#accordion" | + | <a data-toggle="collapse" data-parent="#accordion" href="#collapseFour"> |
− | + | Week 9 | |
</a> | </a> | ||
</h4> | </h4> | ||
</div> | </div> | ||
− | <div id=" | + | <div id="collapseFour" class="panel-collapse collapse"> |
<div class="panel-body"> | <div class="panel-body"> | ||
− | + | transform the plasmid pBBR1-kan-amp-ccdb-BAD-GFP-firefly into GB05 red gyrA462 via electroporation. Do Mini-Prep and screen correct plasmid by restriction analysis. | |
− | + | ||
</div> | </div> | ||
</div> | </div> | ||
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<div class="panel-heading"> | <div class="panel-heading"> | ||
<h4 class="panel-title"> | <h4 class="panel-title"> | ||
− | <a data-toggle="collapse" data-parent="#accordion" | + | <a data-toggle="collapse" data-parent="#accordion" href="#collapseFive"> |
− | + | Week 10 | |
</a> | </a> | ||
</h4> | </h4> | ||
</div> | </div> | ||
− | <div id=" | + | <div id="collapseFive" class="panel-collapse collapse"> |
<div class="panel-body"> | <div class="panel-body"> | ||
− | + | construct the plasmid pBBR1-kan-cm-promoter(1-25)-firefly via liner circular recombination in GB05 red gyrA462. Do Mini-Prep and screen correct recombinants by restriction analysis. | |
− | + | ||
</div> | </div> | ||
</div> | </div> | ||
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<div class="panel-heading"> | <div class="panel-heading"> | ||
<h4 class="panel-title"> | <h4 class="panel-title"> | ||
− | <a data-toggle="collapse" data-parent="#accordion" | + | <a data-toggle="collapse" data-parent="#accordion" href="#collapseSix"> |
− | + | Week 11 | |
</a> | </a> | ||
</h4> | </h4> | ||
</div> | </div> | ||
− | <div id=" | + | <div id="collapseSix" class="panel-collapse collapse"> |
<div class="panel-body"> | <div class="panel-body"> | ||
− | + | transform the plasmid pBBR1-kan-amp-ccdb-BAD-GFP-firefly into p.fluorescence pf-5 via electroporation. | |
</div> | </div> | ||
</div> | </div> | ||
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<div class="panel-heading"> | <div class="panel-heading"> | ||
<h4 class="panel-title"> | <h4 class="panel-title"> | ||
− | <a data-toggle="collapse" data-parent="#accordion" | + | <a data-toggle="collapse" data-parent="#accordion" href="#collapseSeven"> |
− | + | Week 12 & 13 | |
</a> | </a> | ||
</h4> | </h4> | ||
</div> | </div> | ||
− | <div id=" | + | <div id="collapseSeven" class="panel-collapse collapse"> |
<div class="panel-body"> | <div class="panel-body"> | ||
− | + | chracterize the strength of different promoters by luciferase firefly assay. | |
− | + | ||
</div> | </div> | ||
</div> | </div> | ||
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<div class="panel-heading"> | <div class="panel-heading"> | ||
<h4 class="panel-title"> | <h4 class="panel-title"> | ||
− | <a data-toggle="collapse" data-parent="#accordion" | + | <a data-toggle="collapse" data-parent="#accordion" href="#collapseEight"> |
− | + | Week 14 - 17 | |
</a> | </a> | ||
</h4> | </h4> | ||
</div> | </div> | ||
− | <div id=" | + | <div id="collapseEight" class="panel-collapse collapse"> |
<div class="panel-body"> | <div class="panel-body"> | ||
− | + | modeling | |
− | + | ||
</div> | </div> | ||
</div> | </div> | ||
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<div class="panel-heading"> | <div class="panel-heading"> | ||
<h4 class="panel-title"> | <h4 class="panel-title"> | ||
− | <a data-toggle="collapse" data-parent="#accordion" | + | <a data-toggle="collapse" data-parent="#accordion" href="#collapseNine"> |
− | + | Week 17 - 20 | |
</a> | </a> | ||
</h4> | </h4> | ||
</div> | </div> | ||
− | <div id=" | + | <div id="collapseNine" class="panel-collapse collapse"> |
<div class="panel-body"> | <div class="panel-body"> | ||
− | + | constract our software tool | |
</div> | </div> | ||
</div> | </div> | ||
</div> | </div> | ||
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</div> | </div> | ||
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Revision as of 14:09, 15 October 2018
Find promoters with various strength in the light of transcriptom references. Take the sequence from the upstream of a specific gene.
design the PAGE-purified oligonucleotides used to amplify the chloramphenicol and add homology arm for rencombination.
amplify the chloramphnicol and promoter segment and add vector homology arms via series PCR. Purify the PCR products using the TianGen PCR Purification Kit and elute into 30ul of autoclaved ddH2O. Quantify the elution using a NanoDrop UV spectrophotometer, store them at 4℃
transform the plasmid pBBR1-kan-amp-ccdb-BAD-GFP-firefly into GB05 red gyrA462 via electroporation. Do Mini-Prep and screen correct plasmid by restriction analysis.
construct the plasmid pBBR1-kan-cm-promoter(1-25)-firefly via liner circular recombination in GB05 red gyrA462. Do Mini-Prep and screen correct recombinants by restriction analysis.
transform the plasmid pBBR1-kan-amp-ccdb-BAD-GFP-firefly into p.fluorescence pf-5 via electroporation.
chracterize the strength of different promoters by luciferase firefly assay.
modeling
constract our software tool