Difference between revisions of "Team:CCU Taiwan/Entrepreneurship"

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<p>This page is used by the judges to evaluate your team for the <a href="https://2017.igem.org/Judging/Medals">medal criterion</a> or <a href="https://2017.igem.org/Judging/Awards"> award listed above</a>. </p>
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<div class="inner">
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<header>
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<h1><a href="https://2017.igem.org/Team:CCU_Taiwan" id="logo">Entrepreneurship</a></h1>
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</header>
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</div>
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<!-- Nav -->
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<nav id="nav">
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<ul>
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 +
 
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<li>
 +
<a href="#">Project</a>
 +
<ul>
 +
<li><a href="#">Description</a></li>
 +
                                                                                <li>
 +
<a href="#">Biosensor</a>
 +
<ul>
 +
<li><a href="#">CSP detector</a></li>
 +
<li><a href="#">Lactate detector</a></li>
 +
</ul>
 +
</li>
 +
<li><a href="#">Modeling</a></li>
 +
<li><a href="#">Experiment</a></li>
 +
 +
<li><a href="Results">Result</a></li>
 +
<li><a href="#">Future perspective</a></li>
 +
<li><a href="#">Safty</a></li>
 +
</ul>
 +
</li>
 +
 
 +
<li>
 +
<a href="#">Dry lab</a>
 +
<ul>
 +
                                                                                <li>
 +
<a href="#">Hardware</a>
 +
<ul>
 +
<li><a href="#">Device</a></li>
 +
<li><a href="#">Detector</a></li>
 +
</ul>
 +
</li>
 +
 
 +
                                                                                <li>
 +
<a href="#">Software</a>
 +
<ul>
 +
<li><a href="#">IOT system</a></li>
 +
<li><a href="#">APP</a></li>
 +
                                                                                                <li><a href="#">Machine learning</a></li>
 +
</ul>
 +
</li>
 +
</ul>
 +
</li>
 +
 
 +
 
 +
<li>
 +
<a href="#">Human practice</a>
 +
<ul>
 +
<li><a href="#">Silver</a></li>
 +
<li><a href="#">Gold and Integrated</a></li>
 +
<li><a href="#">Engagemant</a></li>
 +
<li><a href="#">Entrepreneurship</a></li>
 +
</ul>
 +
</li>
 +
 
 +
<li>
 +
<a href="#">Part</a>
 +
<ul>
 +
<li><a href="#">Basic part</a></li>
 +
<li><a href="#">Composite part</a></li>
 +
 +
</ul>
 +
</li>
 +
 
 +
 
 +
<li>
 +
<a href="#">Notebook</a>
 +
<ul>
 +
<li><a href="#">Schedule</a></li>
 +
<li><a href="#">Protocol</a></li>
 +
<li><a href="https://2017.igem.org/Team:CCU_Taiwan/InterLab">InterLab</a></li>
 +
 +
</ul>
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</li>
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 +
 
 +
<li>
 +
<a href="#">Team</a>
 +
<ul>
 +
<li><a href="https://2017.igem.org/Team:CCU_Taiwan/Member">Member</a></li>
 +
<li><a href="https://2017.igem.org/Team:CCU_Taiwan/Collaborations">Collaborations</a></li>
 +
<li><a href="#">Attribution</a></li>
 +
 +
</ul>
 +
</li>
 +
 
 +
 
 +
<li>
 +
<a href="#">Judging</a>
 +
<ul>
 +
<li><a href="#">Gold</a></li>
 +
<li><a href="#">Silver</a></li>
 +
<li><a href="#">Bronze</a></li>
 +
 +
</ul>
 +
</li>
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<li><a href="no-sidebar.html">Q&A</a></li>
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</ul>
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<div class="container">
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<article id="main" class="special">
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<header>
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<div class="div_nav">
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<nav class="toc_nav" id="toc_show">
 +
<ul>
 +
<li>
 +
<a href="#Fluorescein">Fluorescein curve</a>
 +
<ul>
 +
<li><a href="#Fluorescein-Plate-reader">Plate reader</a></li>
 +
<li><a href="#Fluorescein-Material">Material</a></li>
 +
<li><a href="#Fluorescein-Method">Method</a></li>
 +
<li><a href="#Fluorescein-Data-result">Data result</a></li>
 +
</ul>
 +
</li>
 +
<li>
 +
<a href="#OD600">OD600 Reference point</a>
 +
      <ul>
 +
<li><a href="#OD600-Plate-reader">Plate reader</a></li>
 +
<li><a href="#OD600-Material">Material</a></li>
 +
<li><a href="#OD600-Method">Method</a></li>
 +
<li><a href="#OD600-Data-result">Data result</a></li>
 +
      </ul>
 +
</li>
 +
 
 +
<li>
 +
<a href="#Cell">Cell measure</a>
 +
      <ul>
 +
<li><a href="#Cell-Material">Material</a></li>
 +
<li><a href="#Cell-Method">Method</a></li>
 +
<li><a href="#Cell-Data-result">Data result</a></li>
 +
      </ul>
 +
</li>
 +
 
 +
 
 +
</ul>
 +
  <svg class="toc-marker" width="200" height="200" xmlns="http://www.w3.org/2000/svg">
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    <path stroke="#444" stroke-width="3" fill="transparent" stroke-dasharray="0, 0, 0, 1000" stroke-linecap="round" stroke-linejoin="round" transform="translate(-0.5, -0.5)" />
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</nav>
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<article class="contents_nav">
 +
  <section>
 +
 
 +
 
 +
<div id="Fluorescein">
 +
<h2>Fluorescein Fluorescence standard curve</h2>
 +
<div class="aaa"></div>
 
</div>
 
</div>
−
<div class="clear"></div>
 
  
 +
<div id="Fluorescein-Plate-reader">
  
 +
<h3>Plate reader</h3>
  
−
<div class="column half_size">
+
    <p>
−
<h1>Entrepreneurship</h1>
+
      microplate reader FLUOstar Omega</br>
−
<h3>Best Supporting Entrepreneurship Special Prize</h3>
+
emission filter: 520 nm</br>
 +
excitation filter: 485 nm
 +
    </p>
 +
<div class="aaa"></div>
 +
</div>
 +
 
 +
<div id="Fluorescein-Material">
 +
 
 +
<h3>Material</h3>
 +
<p>
 +
Fluorescein sodium salt</br>
 +
1xPBS</br>
 +
Tissue culture testplate (black with flat bottom)
 +
</p>
 +
<div class="aaa"></div>
 +
</div>
 +
 
 +
<div id="Fluorescein-Method">
 +
 
 +
                <h3>Method</h3>
 +
 +
<ol><li>Prepare fluorescein stock solution</li></ol>
 
<p>
 
<p>
−
In previous years, iGEM had an entrepreneurship track. Teams were encouraged to build projects and focus around commercializing their work. We have now moved to an award as the best work in this area may come from teams who are not solely focused on entrepreneurship.  
+
1. Spin down fluorescein stock tube to make sure pellet is at the bottom of tube.</br>
 +
2. Prepare 2x fluorescein stock solution (100 μM) by resuspending fluorescein in 1 mL of 1xPBS. </br>
 +
3. Dilute the 2x fluorescein stock solution with 1xPBS to make a 1x fluorescein solution and resulting concentration of fluorescein  stock solution 50 μM </br></br>
 
</p>
 
</p>
 +
<ol><li>Serial dilutions</li></ol>
 +
<p>
 +
1. Add 100 μl of PBS into wells A2, B2, C2, D2....A12, B12, C12, D12</br>
 +
2. Add 200 μl of fluorescein 1x stock solution into A1, B1, C1, D1</br>
 +
3. Transfer 100 μl of fluorescein stock solution from A1 into A2. </br>
 +
4. Mix A2 by pipetting up and down 3x and transfer 100 μl into A3. </br>
 +
5. Mix A3 by pipetting up and down 3x and transfer 100 μl into A4. </br>
 +
6. Mix A4 by pipetting up and down 3x and transfer 100 μl into A5. </br>
 +
7. Mix A5 by pipetting up and down 3x and transfer 100 μl into A6. </br>
 +
8. Mix A6 by pipetting up and down 3x and transfer 100 μl into A7. </br>
 +
9. Mix A7 by pipetting up and down 3x and transfer 100 μl into A8. </br>
 +
10. Mix A8 by pipetting up and down 3x and transfer 100 μl into A9. </br>
 +
11. Mix A9 by pipetting up and down 3x and transfer 100 μl into A10.</br>
 +
12. Mix A10 by pipetting up and down 3x and transfer 100 μl into A11. </br>
 +
13. Mix A11 by pipetting up and down 3x and transfer 100 μl into liquid waste.
 +
  (Caution: Do not to continue serial dilution into column 12.)</br>
 +
</p>
 +
<ol><li>repeat serial dilute for Row B、D、E</strong></li></ol>
 +
<ol><li>Measure fluorescence of all samples in all standard measurement modes in instrument Record the data in your notebook</strong></li></ol>
 +
<ol><li>Import data into Excel (fluorescein standard curve tab ) Sheet_1 provided</li></ol>
 +
 +
<br/><br/>
 +
<div class="aaa"></div>
 +
</div>
 +
<div id="Fluorescein-Data-result">
  
−
<p>The Best Supporting Entrepreneurship award recognizes exceptional effort to build a business case and commercialize an iGEM project. This award is open to all teams to show that entrepreneurship is something all teams can aspire to do with their project. This award can go to an new project, or to a previous project that a team aimed to commercialize. Have you filed a provisional patent on your project/device/process? Have you raised money to build and ship products? Have you pitched your idea to investors and received money? As always in iGEM, the aim is to impress the judges!
+
<h3>Data result</h3>
 +
<br/>
 +
<img src="https://static.igem.org/mediawiki/2017/8/85/FFs_1.png" style="display:block; margin:auto;"><br/><br/>
 +
<img src="https://static.igem.org/mediawiki/2017/a/a4/FFs_2.png" style="display:block; margin:auto;"><br/><br/>
 +
<img src="https://static.igem.org/mediawiki/2017/5/5c/FFs_3.png" style="display:block; margin:auto;"><br/>
 +
</div>
 +
</section>
  
−
<br><br>
+
<section>
−
To compete for the <a href="https://2017.igem.org/Judging/Awards">Best Supporting Entrepreneurship prize</a>, please describe your work on this page and also fill out the description on the <a href="https://2017.igem.org/Judging/Judging_Form">judging form</a>.
+
 
−
<br><br>
+
 
−
You must also delete the message box on the top of this page to be eligible for this prize.
+
<div id="OD600">
−
</p>
+
<h2>OD600 Reference point</h2>
 +
<div class="aaa"></div>
 +
</div>
 +
 
 +
 
 +
<div id="OD600-Plate-reader">
 +
 
 +
<h3>Plate reader</h3>
 +
 
 +
    <p>
 +
Thermo Scientific™ Multiskan™ FC Filter-based Microplate Photometer</br>
 +
Filter: 595 nm</br>
 +
    </p>
 +
<div class="aaa"></div>
 +
</div>
 +
 
 +
<div id="OD600-Material">
 +
 
 +
<h3>Material</h3>
 +
<p>
 +
1 ml LUDOX</br>
 +
mQH<sub>2</sub>O</br>
 +
96 well cell culture plate (clear with flat-bottom)
 +
</p>
 +
<div class="aaa"></div>
 +
</div>
 +
 
 +
<div id="OD600-Method">
 +
 
 +
                <h3>Method</h3>
 +
 
 +
<p>
 +
1. Add 100 μl LUDOX into wells A1, B1, C1, D1 (or 1 mL LUDOX into cuvette)</br>
 +
2. Add 100 μl of H<sub>2</sub>O into wells A2, B2, C2, D2 (or 1 mL H<sub>2</sub>O into cuvette)</br>
 +
3. Measure absorbance 600 nm of all samples in all standard measurement modes in instrument</br>
 +
4. Record the data in excel and Import data into Excel ( OD600 reference point tab ) Sheet_1 provided</br>
 
</p>
 
</p>
 +
<div class="aaa"></div>
 
</div>
 
</div>
  
−
<div class="column half_size">
+
<div id="OD600-Data-result">
  
−
<h5>Inspiration</h5>
+
<h3>Data result</h3>
−
<p>You can look at what other teams did to get some inspiration! <br />
+
<br/>
−
Here are a few examples:</p>
+
<img src="https://static.igem.org/mediawiki/2017/5/5a/600_1.png" style="display:block; margin:auto;"><br/>
−
<ul>
+
</div>
−
<li><a href="https://2016.igem.org/Team:Sydney_Australia">2016 Sydney Australia</a></li>
+
</section>
−
<li><a href="https://2016.igem.org/Team:Pasteur_Paris">2016 Pasteur Paris</a></li>
+
−
<li><a href="https://2014.igem.org/Team:UCC_Ireland">2014 UCC Ireland</a></li>
+
−
<li><a href="https://2014.igem.org/Team:Imperial">2014 Imperial College London</a></li>
+
−
</ul>
+
  
−
<h5>Patents and intellectual property</h5>
+
<section>
 +
 
 +
 
 +
<div id="Cell">
 +
<h2>Cell measure</h2>
 +
<div class="aaa"></div>
 +
</div>
 +
 
 +
 
 +
<div id="Cell-Material">
 +
 
 +
<h3>Material</h3>
 +
<p>
 +
Competent cells ( Escherichia coli strain DH5α)</br>
 +
LB (Luria Bertani) media</br>
 +
Chloramphenicol (stock concentration 25 mg/mL dissolved in EtOH - working stock 25 μg /mL)</br>
 +
50 ml Falcon tube (or equivalent, preferably amber or covered in foil to block light)</br>
 +
Incubator at 37°C</br>
 +
1.5 ml eppendorf tubes for sample storage</br>
 +
Ice bucket with ice</br>
 +
Pipettes</br>
 +
96 well plate(cell culture 96 well plate、tissue culture testplate)</br>
 +
Devices (from InterLab Measurement Kit):</br>
 +
1. Negative control(BBa_R0040)</br>
 +
2. Positive control(J23151+B0032+E0040+B0010+B0012)</br>
 +
3. Test Device 1: J23101+I13504</br>
 +
4. Test Device 2: J23106+I13504</br>
 +
5. Test Device 3: J23117+I13504</br>
 +
6. Test Device 4: J23101+BCD2+E0040+B0015</br>
 +
7. Test Device 5: J23106+BCD2+E0040+B0015</br>
 +
8. Test Device 6: J23117+BCD2+E0040+B0015</br>
 +
</p>
 +
<div class="aaa"></div>
 +
</div>
 +
 
 +
<div id="Cell-Method">
 +
 
 +
                <h3>Method</h3>
  
 
<p>
 
<p>
−
If your team is seriously considering commercializing and looking into building a company after the competition, you may want to look at how you are going to protect your work and secure investment. Investors will usually require some form of intellectual protection, so you may want to investigate how to apply for a patent or provisional patent in your country and region before disclosing your project at iGEM. Remember that you can only be evaluated in iGEM based on what you share on your wiki and at the Jamboree, so any work you don't present can't count towards your project. </p>
+
1. Day 1 : Resuspended each plasmid in plate 7 and transform into Escherichia coli DH5α.</br>
 +
&nbsp;(Transformation protocol is from iGEM)</br>
 +
2. Day 2 : Pick 2 colonies from each of plate and inoculate it on 5-10 mL LB medium +Chloramphenicol.Grow the cells overnight (16-18 hours) at 37°C and 170 rpm.</br>
 +
3. Day 3 : Set instrument to read OD600 (as OD calibration setting)and measure OD600 of the overnight cultures</br>
 +
4. Dilute the cultures to a target OD 600 of 0.02 in 12 ml LB medium + Chloramphenicol in 50 mL falcon tube (covered with foil to block light).</br>
 +
5. Incubate the cultures at 37°C and 170 rpm.</br>
 +
6. Take 1000 μL samples of the cultures at 0, 2, 4, and 6 hours of incubation and place samples on ice</br>
 +
7. 4 replicates of 100 uL samples were taken from each culture at 0, 2, 4, and 6 hours of incubation and placed in a 96 well plate for OD and fluorescence measurements using the setup described above</br>
 +
</p>
 +
<div class="aaa"></div>
 +
</div>
  
−
<p>This is an area where we are different as we care about sharing, openness and contributing to the community and investors don't always agree with these values. It is up to you and your team to decide what to do. Remember that most universities have a commercialization department and that you can talk to them before coming to a decision.
+
<div id="Cell-Data-result">
−
</p>  
+
  
 +
<h3>Data result</h3>
 +
<br/>
 +
<img src="https://static.igem.org/mediawiki/2017/3/30/Cell_1.png" style="display:block; margin:auto;"><br/><br/>
 +
<img src="https://static.igem.org/mediawiki/2017/f/fe/Cell_2.png" style="display:block; margin:auto;"><br/>
 
</div>
 
</div>
 +
</section>
 +
 +
</article>
 +
</div>
 +
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Revision as of 02:25, 27 October 2017

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Fluorescein Fluorescence standard curve

Plate reader

microplate reader FLUOstar Omega
emission filter: 520 nm
excitation filter: 485 nm

Material

Fluorescein sodium salt
1xPBS
Tissue culture testplate (black with flat bottom)

Method

  1. Prepare fluorescein stock solution

1. Spin down fluorescein stock tube to make sure pellet is at the bottom of tube.
2. Prepare 2x fluorescein stock solution (100 μM) by resuspending fluorescein in 1 mL of 1xPBS.
3. Dilute the 2x fluorescein stock solution with 1xPBS to make a 1x fluorescein solution and resulting concentration of fluorescein stock solution 50 μM

  1. Serial dilutions

1. Add 100 μl of PBS into wells A2, B2, C2, D2....A12, B12, C12, D12
2. Add 200 μl of fluorescein 1x stock solution into A1, B1, C1, D1
3. Transfer 100 μl of fluorescein stock solution from A1 into A2.
4. Mix A2 by pipetting up and down 3x and transfer 100 μl into A3.
5. Mix A3 by pipetting up and down 3x and transfer 100 μl into A4.
6. Mix A4 by pipetting up and down 3x and transfer 100 μl into A5.
7. Mix A5 by pipetting up and down 3x and transfer 100 μl into A6.
8. Mix A6 by pipetting up and down 3x and transfer 100 μl into A7.
9. Mix A7 by pipetting up and down 3x and transfer 100 μl into A8.
10. Mix A8 by pipetting up and down 3x and transfer 100 μl into A9.
11. Mix A9 by pipetting up and down 3x and transfer 100 μl into A10.
12. Mix A10 by pipetting up and down 3x and transfer 100 μl into A11.
13. Mix A11 by pipetting up and down 3x and transfer 100 μl into liquid waste. (Caution: Do not to continue serial dilution into column 12.)

  1. repeat serial dilute for Row B、D、E
  1. Measure fluorescence of all samples in all standard measurement modes in instrument Record the data in your notebook
  1. Import data into Excel (fluorescein standard curve tab ) Sheet_1 provided


Data result







OD600 Reference point

Plate reader

Thermo Scientific™ Multiskan™ FC Filter-based Microplate Photometer
Filter: 595 nm

Material

1 ml LUDOX
mQH2O
96 well cell culture plate (clear with flat-bottom)

Method

1. Add 100 μl LUDOX into wells A1, B1, C1, D1 (or 1 mL LUDOX into cuvette)
2. Add 100 μl of H2O into wells A2, B2, C2, D2 (or 1 mL H2O into cuvette)
3. Measure absorbance 600 nm of all samples in all standard measurement modes in instrument
4. Record the data in excel and Import data into Excel ( OD600 reference point tab ) Sheet_1 provided

Data result



Cell measure

Material

Competent cells ( Escherichia coli strain DH5α)
LB (Luria Bertani) media
Chloramphenicol (stock concentration 25 mg/mL dissolved in EtOH - working stock 25 μg /mL)
50 ml Falcon tube (or equivalent, preferably amber or covered in foil to block light)
Incubator at 37°C
1.5 ml eppendorf tubes for sample storage
Ice bucket with ice
Pipettes
96 well plate(cell culture 96 well plate、tissue culture testplate)
Devices (from InterLab Measurement Kit):
1. Negative control(BBa_R0040)
2. Positive control(J23151+B0032+E0040+B0010+B0012)
3. Test Device 1: J23101+I13504
4. Test Device 2: J23106+I13504
5. Test Device 3: J23117+I13504
6. Test Device 4: J23101+BCD2+E0040+B0015
7. Test Device 5: J23106+BCD2+E0040+B0015
8. Test Device 6: J23117+BCD2+E0040+B0015

Method

1. Day 1 : Resuspended each plasmid in plate 7 and transform into Escherichia coli DH5α.
 (Transformation protocol is from iGEM)
2. Day 2 : Pick 2 colonies from each of plate and inoculate it on 5-10 mL LB medium +Chloramphenicol.Grow the cells overnight (16-18 hours) at 37°C and 170 rpm.
3. Day 3 : Set instrument to read OD600 (as OD calibration setting)and measure OD600 of the overnight cultures
4. Dilute the cultures to a target OD 600 of 0.02 in 12 ml LB medium + Chloramphenicol in 50 mL falcon tube (covered with foil to block light).
5. Incubate the cultures at 37°C and 170 rpm.
6. Take 1000 μL samples of the cultures at 0, 2, 4, and 6 hours of incubation and place samples on ice
7. 4 replicates of 100 uL samples were taken from each culture at 0, 2, 4, and 6 hours of incubation and placed in a 96 well plate for OD and fluorescence measurements using the setup described above

Data result