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<h3>★  ALERT! </h3>
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<p>This page is used by the judges to evaluate your team for the <a href="https://2018.igem.org/Judging/Medals">medal criterion</a> or <a href="https://2018.igem.org/Judging/Awards"> award listed below</a>. </p>
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<p> Delete this box in order to be evaluated for this medal criterion and/or award. See more information at <a href="https://2018.igem.org/Judging/Pages_for_Awards"> Instructions for Pages for awards</a>.</p>
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<h1>InterLab</h1>
 
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<h3>Bronze Medal Criterion #4</h3>
 
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<p><b>Standard Tracks:</b> Participate in the Interlab Measurement Study and/or obtain new, high quality experimental characterization data for an existing BioBrick Part or Device and enter this information on that part's Main Page in the Registry. The part that you are characterizing must NOT be from a 2018 part number range.
 
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<br><br>
 
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For teams participating in the <a href="https://2018.igem.org/Measurement/InterLab">InterLab study</a>, all work must be shown on this page.
 
  
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                        <div class="fl_l"><h3>INTERLAB</h3></div>
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<menu id="tocc" class="hide-on-med-and-down" style="padding: 0.1px; left: 0px; z-index:1; font-family:'Candara',sans-serif;">
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<ul class="fl_l" style="margin-top:200px; opacity:0;">
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                                        <li><a href="#">Background</a></li>
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                                        <li><a href="#">Overview</a></li>
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<li><a href="#">Results and discussion</a></li>
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                                        <li><a href="#">Conclusion</a></li>
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</ul>
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<ul class="fl_r">
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<li>
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        <div class="bigtitle">
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            Background
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        </div>
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        <div class="zhengwen">
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            This is the second time that we have participated in International Interlaboratory Study along with many other teams from around the world. Interlab studies is used to compare the results in different labs around the world.  This study is organized by iGEM’s measurement committee in an effort to establish standardized, reliable and repeatable measurement tools for the iGEM community and the synthetic biology community as a whole. The objective of this year’s Interlab is to establish a GFP measurement protocol through measurement three calibration and cell measurement protocol.
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        </div>
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    </li>
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    <li>
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        <div class="bigtitle">
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            Overview
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        </div>
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        <div class="zhengwen">
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            According to the requirements, we completed calibration protocols first. We made three sets of unit calibration measurements: an OD600 reference point, a particle standard curve, and a fluorescein standard curve. In all three calibration measurements, we used the same plates and volumes in cell-based assays. For the plate reader our excitation and emission settings were 485 nm and 530 nm respectively (Same setting was used for all experiments below).In the process of the experiment, the measurement of the three calibration were remarkable smooth.
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        </div>
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        <div class="zhengwen">
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            But in restrict of experiment condition, we met a lot of difficulties in cell measurement experiment. In addition, cell measurement was not as good as expected at the first time, so we repeated the cell measurement experiment and sequencing was used to verify the success of the transformation. At last, we get the corrected results after repeat multiple times.
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        </div>
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    </li>
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    <li>
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        <div class="bigtitle">
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            Results and discussion
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        </div>
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        <div class="smtitle">
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            Measurement of standard curve
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        </div>
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        <div class="zhengwen">
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            We measured the LUDOX CL-X , Microsphere suspension and Fluorescein to obtain the following results. In this way we can transform absorbance data into a standard OD600 measurement and we obtain a Particle Standard Curve and a Fluorescence standard curve.
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        </div>
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        <div class="chatu" style="padding:20px 10%;"><img src="https://static.igem.org/mediawiki/2018/b/bf/T--UESTC-China--interlabhhhhh1.jpg" width="100%"></div>
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        <div class="tu">Fig. 1 &nbsp;Using fluorescein to plot fluorescence standard curve</div>
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        <div class="chatu" style="padding:20px 10%;"><img src="https://static.igem.org/mediawiki/2018/0/0e/T--UESTC-China--interlab2222222.jpg" width="100%"></div>
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        <div class="tu">Fig. 2 &nbsp;Fluorescence is plotted in a log scale to demonstrate a linear relationship.</div>
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        <div class="smtitle">
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            Cell measurement
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        </div>
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        <div class="zhengwen">Devices: Positive control: BBa_I20270、Negative control: BBa_R0040、</div>
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        <div class="zhengwen">Device 1: BBa_J364000、Device 2: BBa_J364001、Device 3: BBa_J364002、</div>
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        <div class="zhengwen">Device 4: BBa_J364003、Device 5: BBa_J364004、Device 6: BBa_J364005</div>
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        <div class="zhengwen">Microorganism: Escherichia coli DH5⍺ strains</div>
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        <div class="zhengwen">The protocol was easy to follow and the constructs were nicely expressed which makes our measurements more reliable and comparable. After 0 and 6 hours, we measured the OD600 and the fluorescence of the transformed cells according to the protocol. We obtained the following data from the measurement and use the three standard curves to calculate the data.</div>
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        <div class="zhengwen">
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            <table class="table table-hover">
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                <tr><td></td><td> 1 </td><td>2</td><td> 3 </td><td>4 </td><td>5</td><td> 6</td><td> 7</td><td> 8 </td><td>9 </td><td>10 </td><td>11 </td><td>12</td></tr>
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                <tr><td> A</td><td> Neg. Control 1-1</td><td> Pos. Control 1-1</td><td> Device 1 1-1</td><td> Device 2 1-1</td><td> Device 3 1-1</td><td> Device 4 1-1</td><td> Device 5 1-1</td><td> Device 6 1-1</td><td> LB+Chl</td><td> Empty</td><td> Empty</td><td> Empty</td></tr>
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                <tr><td> B </td><td>Neg. Control 1-2 </td><td>Pos. Control 1-2 </td><td>Device 1 1-2 </td><td>Device 2 1-2 </td><td>Device 3 1-2 </td><td>Device 4 1-2 </td><td>Device 5 1-2 </td><td>Device 6 1-2</td><td> LB+Chl </td><td>Empty</td><td> Empty</td><td> Empty</td></tr>
 +
                <tr><td> C</td><td> Neg. Control 1-3</td><td> Pos. Control 1-3</td><td> Device 1 1-3</td><td> Device 2 1-3</td><td> Device 3 1-3</td><td> Device 4 1-3</td><td> Device 5 1-3</td><td> Device 6 1-3</td><td> LB+Chl</td><td> Empty</td><td> Empty</td><td> Empty</td></tr>
 +
                <tr><td>D </td><td>Neg. Control 1-4 </td><td>Pos. Control 1-4</td><td> Device 1 1-4</td><td> Device 2 1-4</td><td> Device 3 1-4</td><td> Device 4 1-4</td><td> Device 5 1-4</td><td> Device 6 1-4</td><td> LB+Chl</td><td> Empty</td><td> Empty</td><td> Empty</td></tr>
 +
                <tr><td>E </td><td>Neg. Control 2-1 </td><td>Pos. Control 2-1</td><td> Device 1 2-1</td><td> Device 2 2-1</td><td> Device 3 2-1</td><td> Device 4 2-1</td><td> Device 5 2-1</td><td> Device 6 2-1</td><td> LB+Chl</td><td> Empty</td><td> Empty</td><td> Empty</td></tr>
 +
                <tr><td>F </td><td>Neg. Control 2-2 </td><td>Pos. Control 2-2</td><td> Device 1 2-2</td><td> Device 2 2-2</td><td> Device 3 2-2</td><td> Device 4 2-2</td><td> Device 5 2-2</td><td> Device 6 2-2</td><td> LB+Chl</td><td> Empty</td><td> Empty</td><td> Empty</td></tr>
 +
                <tr><td>G </td><td>Neg. Control 2-3 </td><td>Pos. Control 2-3</td><td> Device 1 2-3</td><td> Device 2 2-3</td><td> Device 3 2-3</td><td> Device 4 2-3</td><td> Device 5 2-3</td><td> Device 6 2-3</td><td> LB+Chl</td><td> Empty</td><td> Empty</td><td> Empty</td></tr>
 +
                <tr><td>H </td><td>Neg. Control 2-4 </td><td>Pos. Control 2-4</td><td> Device 1 2-4</td><td> Device 2 2-4</td><td> Device 3 2-4</td><td> Device 4 2-4</td><td> Device 5 2-4</td><td> Device 6 2-4</td><td> LB+Chl</td><td> Empty</td><td> Empty</td><td> Empty</td></tr>
 +
 
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            </table>
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        </div>
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        <div class="tu">Fig. 3 &nbsp;Sketch map of plate pattern</div>
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        <div class="chatu" style="padding:20px 10%;"><img src="https://static.igem.org/mediawiki/2018/2/26/T--UESTC-China--int4.png" width="100%"></div>
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        <div class="tu">Fig. 4 &nbsp;The difference of fluorescence raw readings between colony 1 0h and 6h</div>
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        <div class="chatu" style="padding:20px 10%;"><img src="https://static.igem.org/mediawiki/2018/7/73/T--UESTC-China--int444444444.jpg" width="100%"></div>
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        <div class="tu">Fig. 5 &nbsp;The difference of fluorescence raw readings between colony 2 0h and 6h</div>
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        <div class="chatu" style="padding:20px 10%;"><img src="https://static.igem.org/mediawiki/2018/a/a1/T--UESTC-China--interlab6666666666.gif" width="100%"></div>
 +
        <div class="tu">Fig. 6 &nbsp;The difference of fluorescence raw readings between 0h and 6h</div>
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        <div class="zhengwen">
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            Compare the devices we can found that the different promoters will influence the expression of proteins. We can easily found that the promoters in test 1 and 4 is obviously stronger than the promoters in test device 3 and 6, for the GFP expression is higher than former.
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        <div class="bigtitle">
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            Conclusion
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        <div class="zhengwen">
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            We can find that the best fluorescence results is even higher than positive control. Device 4 shows the best fluorescence, but the absorbance values is not the highest. Device 3 shows us that the values of fluorescence almost no growth, but the absorbance values is the highest. At last, the data suggest that the Interlab study was successful and the protocol can be shared in the community and between the laboratories.
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Latest revision as of 17:00, 17 October 2018

team

INTERLAB

  • Background
    This is the second time that we have participated in International Interlaboratory Study along with many other teams from around the world. Interlab studies is used to compare the results in different labs around the world. This study is organized by iGEM’s measurement committee in an effort to establish standardized, reliable and repeatable measurement tools for the iGEM community and the synthetic biology community as a whole. The objective of this year’s Interlab is to establish a GFP measurement protocol through measurement three calibration and cell measurement protocol.
  • Overview
    According to the requirements, we completed calibration protocols first. We made three sets of unit calibration measurements: an OD600 reference point, a particle standard curve, and a fluorescein standard curve. In all three calibration measurements, we used the same plates and volumes in cell-based assays. For the plate reader our excitation and emission settings were 485 nm and 530 nm respectively (Same setting was used for all experiments below).In the process of the experiment, the measurement of the three calibration were remarkable smooth.
    But in restrict of experiment condition, we met a lot of difficulties in cell measurement experiment. In addition, cell measurement was not as good as expected at the first time, so we repeated the cell measurement experiment and sequencing was used to verify the success of the transformation. At last, we get the corrected results after repeat multiple times.
  • Results and discussion
    Measurement of standard curve
    We measured the LUDOX CL-X , Microsphere suspension and Fluorescein to obtain the following results. In this way we can transform absorbance data into a standard OD600 measurement and we obtain a Particle Standard Curve and a Fluorescence standard curve.
    Fig. 1  Using fluorescein to plot fluorescence standard curve
    Fig. 2  Fluorescence is plotted in a log scale to demonstrate a linear relationship.
    Cell measurement
    Devices: Positive control: BBa_I20270、Negative control: BBa_R0040、
    Device 1: BBa_J364000、Device 2: BBa_J364001、Device 3: BBa_J364002、
    Device 4: BBa_J364003、Device 5: BBa_J364004、Device 6: BBa_J364005
    Microorganism: Escherichia coli DH5⍺ strains
    The protocol was easy to follow and the constructs were nicely expressed which makes our measurements more reliable and comparable. After 0 and 6 hours, we measured the OD600 and the fluorescence of the transformed cells according to the protocol. We obtained the following data from the measurement and use the three standard curves to calculate the data.
    1 2 3 4 5 6 7 8 9 10 11 12
    A Neg. Control 1-1 Pos. Control 1-1 Device 1 1-1 Device 2 1-1 Device 3 1-1 Device 4 1-1 Device 5 1-1 Device 6 1-1 LB+Chl Empty Empty Empty
    B Neg. Control 1-2 Pos. Control 1-2 Device 1 1-2 Device 2 1-2 Device 3 1-2 Device 4 1-2 Device 5 1-2 Device 6 1-2 LB+Chl Empty Empty Empty
    C Neg. Control 1-3 Pos. Control 1-3 Device 1 1-3 Device 2 1-3 Device 3 1-3 Device 4 1-3 Device 5 1-3 Device 6 1-3 LB+Chl Empty Empty Empty
    D Neg. Control 1-4 Pos. Control 1-4 Device 1 1-4 Device 2 1-4 Device 3 1-4 Device 4 1-4 Device 5 1-4 Device 6 1-4 LB+Chl Empty Empty Empty
    E Neg. Control 2-1 Pos. Control 2-1 Device 1 2-1 Device 2 2-1 Device 3 2-1 Device 4 2-1 Device 5 2-1 Device 6 2-1 LB+Chl Empty Empty Empty
    F Neg. Control 2-2 Pos. Control 2-2 Device 1 2-2 Device 2 2-2 Device 3 2-2 Device 4 2-2 Device 5 2-2 Device 6 2-2 LB+Chl Empty Empty Empty
    G Neg. Control 2-3 Pos. Control 2-3 Device 1 2-3 Device 2 2-3 Device 3 2-3 Device 4 2-3 Device 5 2-3 Device 6 2-3 LB+Chl Empty Empty Empty
    H Neg. Control 2-4 Pos. Control 2-4 Device 1 2-4 Device 2 2-4 Device 3 2-4 Device 4 2-4 Device 5 2-4 Device 6 2-4 LB+Chl Empty Empty Empty
    Fig. 3  Sketch map of plate pattern
    Fig. 4  The difference of fluorescence raw readings between colony 1 0h and 6h
    Fig. 5  The difference of fluorescence raw readings between colony 2 0h and 6h
    Fig. 6  The difference of fluorescence raw readings between 0h and 6h
    Compare the devices we can found that the different promoters will influence the expression of proteins. We can easily found that the promoters in test 1 and 4 is obviously stronger than the promoters in test device 3 and 6, for the GFP expression is higher than former.
  • Conclusion
    We can find that the best fluorescence results is even higher than positive control. Device 4 shows the best fluorescence, but the absorbance values is not the highest. Device 3 shows us that the values of fluorescence almost no growth, but the absorbance values is the highest. At last, the data suggest that the Interlab study was successful and the protocol can be shared in the community and between the laboratories.
Copyright © 2018 iGEM UESTC-China