Difference between revisions of "Team:Calgary/InterLab"

 
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         <div class="infosection">
 
         <div class="infosection">
             <h3 class="infosubtitle">What is CRISPR?</h3>
+
             <h3 class="infosubtitle">What is the InterLab Study?</h3>
 
             <br>
 
             <br>
          <h5 class="infosubtitle">Kait is cool</h5>
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             <p style="text-indent: 0px">The InterLab study is an international collaborative lab study administered by
             <p style="text-indent: 0px">Lorem ipsum dolor sit amet consectetur adipisicing elit. Consequuntur, totam laudantium, dolor porro laboriosam
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                 the iGEM Measurement Committee and was established several years ago to help create reliable and
                 illo tenetur velit nulla corrupti quasi non eum amet quod dolores, doloremque eius ad temporibus perferendis!
+
                 repeatable measurements in synthetic biology. Ultimately, the goal is to develop a robust measurement
                 Lorem ipsum dolor sit, amet consectetur adipisicing elit. Sit explicabo suscipit similique id expedita cum
+
                 procedure for green fluorescent protein (GFP), which is one of the most commonly used markers in
                 consequatur voluptatibus consectetur adipisci beatae unde, cupiditate inventore. Quis officiis quam porro
+
                 synthetic biology.</p>
                 a expedita non.</p>
+
 
             <br>
 
             <br>
             <p style="text-indent: 0px">Lorem ipsum dolor sit amet consectetur adipisicing elit. Temporibus rerum vel eius ut dolore, ab obcaecati officiis
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             <p style="text-indent: 0px">This year, the purpose of the study was to investigate if the lab-to-lab
                 modi porro, sunt deleniti, consequatur assumenda asperiores aliquid recusandae tenetur neque quae suscipit!
+
                 variability of GFP fluorescence measurements could be reduced by <b>normalizing to absolute cell counts</b>
                 Lorem ipsum dolor sit amet consectetur adipisicing elit. Optio a quam iusto quo, nesciunt odit fuga, similique
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                 or <b>colony-forming units (CFUs).</b></p>
                aspernatur veritatis nemo commodi libero nobis magnam necessitatibus, quidem maiores error debitis minima.
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                Lorem ipsum dolor sit amet consectetur adipisicing elit. Quam ipsum consequatur, deserunt assumenda odio
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                natus. Quis, ea dolor! Voluptas dolore, facere cum illo sunt consectetur nam a soluta optio perferendis.</p>
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             <br>
 
             <br>
             <p style="text-indent: 0px">Lorem ipsum dolor sit, amet consectetur adipisicing elit. Rerum sit perferendis eum delectus odit vero saepe,
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            <h3 class="infosubtitle">Methods</h3>
                 dignissimos aspernatur et libero quisquam minima soluta a suscipit tempora dolores non aliquid ratione? Lorem
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            <br>
                 ipsum dolor, sit amet consectetur adipisicing elit. Sunt excepturi quod, doloribus et asperiores similique
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             <p style="text-indent: 0px">The parts listed below are from the 2018 iGEM Distribution Kit and were
                 tempora, mollitia possimus doloremque officia deleniti eius aut dolorum fuga reiciendis adipisci esse quisquam
+
                transformed into chemically competent <i>E. coli</i> DH5-α cells and were used for all cell
                 quae.
+
                 measurements.</p>
 +
            <img class="info-img" src="https://static.igem.org/mediawiki/2018/1/19/T--Calgary--InterlabPartsStylized.png">
 +
            <br>
 +
            <p><b>Normalizing fluorescence measurements to absolute cell counts:</b></p>
 +
            <p style="text-indent: 0px"><i>E. coli</i> cell concentrations were approximated by comparing the cell
 +
                 absorbance measurements to silica bead absorbance measurements. These silica beads are the same shape
 +
                and size as an <i>E. coli</i> cell, therefore they scatter and absorb light in a similar way. Given
 +
                that the bead concentrations were known, each cell absorbance measurement could be converted to a
 +
                 standard "equivalent concentration of beads".</p>
 +
            <br>
 +
            <p><b>Normalizing to colony-forming units (CFUs):</b></p>
 +
            <p style="text-indent: 0px">The number of CFUs grown after liquid media is poured onto a plate is an
 +
                indication of the number of live cells that were in that media. Using this method with E. coli cells, a
 +
                 conversion factor from absorbance to CFU was computed.
 
             </p>
 
             </p>
 
             <br>
 
             <br>
             <h3 class="infosubtitle">Why CRISPR?</h3>
+
             <p style="text-indent: 0px">The methods and protocols used for this study were distributed by the iGEM
 +
                Measurement Committee and can be found <a href="https://2018.igem.org/Measurement/InterLab/Plate_Reader"
 +
                    target=“_blank”>here</a>.</p>
 
             <br>
 
             <br>
             <p style="text-indent: 0px">Lorem ipsum dolor sit amet consectetur adipisicing elit. Consequuntur, totam laudantium, dolor porro laboriosam
+
            <h3 class="infosubtitle">Results</h3>
                 illo tenetur velit nulla corrupti quasi non eum amet quod dolores, doloremque eius ad temporibus perferendis!
+
            <br>
                 Lorem ipsum dolor sit, amet consectetur adipisicing elit. Sit explicabo suscipit similique id expedita cum
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            <p><b>Calibration</b></p>
                 consequatur voluptatibus consectetur adipisci beatae unde, cupiditate inventore. Quis officiis quam porro
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             <p style="text-indent: 0px">Before we began cell measurements, standard curves were created from the
                 a expedita non.</p>
+
                 absorbance readings and fluorescent measurements of silica bead (particle) and fluorescein serial
 +
                 dilutions. This was done to standardize our absorbance readings and fluorescent measurements. </p>
 +
            <div class="row">
 +
                 <div class="col-lg-6">
 +
                    <img class="info-img2-div" src="https://static.igem.org/mediawiki/2018/1/14/T--Calgary--InterLabParticleStandard.png">
 +
                    <p class="caption">Figure 1. Particle standard curve</p>
 +
                 </div>
 +
                <div class="col-lg-6">
 +
                    <img class="info-img2-div" src="https://static.igem.org/mediawiki/2018/2/25/T--Calgary--InterLabLogParticle.png">
 +
                    <p class="caption">Figure 2. Log particle standard curve</p>
 +
                </div>
 +
            </div>
 +
            <br>
 +
            <div class="row">
 +
                <div class="col-lg-6">
 +
                    <img class="info-img2-div" src="https://static.igem.org/mediawiki/2018/1/18/T--Calgary--InterLabFluorStandard.png">
 +
                    <p class="caption">Figure 3. Fluorescein standard curve</p>
 +
                </div>
 +
                <div class="col-lg-6">
 +
                    <img class="info-img2-div" src="https://static.igem.org/mediawiki/2018/9/98/T--Calgary--InterLabFluorLog.png">
 +
                    <p class="caption">Figure 4. Log fluorescein standard curve</p>
 +
                </div>
 +
            </div>
 +
            <br>
 +
            <br>
 +
            <p><b>Cell Measurements</b></p>
 +
            <br>
 +
            <div class="row">
 +
                <div class="col-lg-6">
 +
                    <img class="info-img2-div" src="https://static.igem.org/mediawiki/2018/8/80/T--Calgary--InterLabNetAbs.png">
 +
                    <p class="caption">Figure 5. Net Abs600 of each device</p>
 +
                </div>
 +
                <div class="col-lg-6">
 +
                    <img class="info-img2-div" src="https://static.igem.org/mediawiki/2018/1/1b/T--Calgary--InterLabNetFluor.png">
 +
                    <p class="caption">Figure 6. Net fluorescein a.u. of each device</p>
 +
                </div>
 +
            </div>
 +
            <br>
 +
            <div class="row">
 +
                <div class="col-lg-3"></div>
 +
                <div class="col-lg-6">
 +
                    <img class="info-img2-div" src="https://static.igem.org/mediawiki/2018/3/33/T--Calgary--InterLabFluorOD.png">
 +
                    <p class="caption">Figure 7. uM fluorescein / OD. This graph accounts for the amount of GFP produced and the number of cells present. </p>
 +
                </div>
 +
                <div class="col-lg-3"></div>
 +
            </div>
 +
            <br>
 +
            <div class="row">
 +
                <div class="col-lg-3"></div>
 +
                <div class="col-lg-6">
 +
                    <img class="info-img2-div" src="https://static.igem.org/mediawiki/2018/4/4d/T--Calgary--InterLabMEFLparticle.png">
 +
                    <p class="caption">Figure 8. MEFL / Particle. This graph accounts for the measure of fluorescence per particle/single cell. </p>
 +
                </div>
 +
                <div class="col-lg-3"></div>
 +
            </div>
 
             <br>
 
             <br>
            <p style="text-indent: 0px">Lorem ipsum dolor sit amet consectetur adipisicing elit. Temporibus rerum vel eius ut dolore, ab obcaecati officiis
 
                modi porro, sunt deleniti, consequatur assumenda asperiores aliquid recusandae tenetur neque quae suscipit!
 
                Lorem ipsum dolor sit amet consectetur adipisicing elit. Optio a quam iusto quo, nesciunt odit fuga, similique
 
                aspernatur veritatis nemo commodi libero nobis magnam necessitatibus, quidem maiores error debitis minima.
 
                Lorem ipsum dolor sit amet consectetur adipisicing elit. Quam ipsum consequatur, deserunt assumenda odio
 
                natus. Quis, ea dolor! Voluptas dolore, facere cum illo sunt consectetur nam a soluta optio perferendis.</p>
 
 
             <br>
 
             <br>
            <p style="text-indent: 0px">Lorem ipsum dolor sit, amet consectetur adipisicing elit. Rerum sit perferendis eum delectus odit vero saepe,
 
                dignissimos aspernatur et libero quisquam minima soluta a suscipit tempora dolores non aliquid ratione? Lorem
 
                ipsum dolor, sit amet consectetur adipisicing elit. Sunt excepturi quod, doloribus et asperiores similique
 
                tempora, mollitia possimus doloremque officia deleniti eius aut dolorum fuga reiciendis adipisci esse quisquam
 
                quae.
 
            </p>
 
 
         </div>
 
         </div>
 
     </div>
 
     </div>

Latest revision as of 00:49, 18 October 2018

Team:Calgary/InterLab - 2018.igem.org

INTERLAB


What is the InterLab Study?


The InterLab study is an international collaborative lab study administered by the iGEM Measurement Committee and was established several years ago to help create reliable and repeatable measurements in synthetic biology. Ultimately, the goal is to develop a robust measurement procedure for green fluorescent protein (GFP), which is one of the most commonly used markers in synthetic biology.


This year, the purpose of the study was to investigate if the lab-to-lab variability of GFP fluorescence measurements could be reduced by normalizing to absolute cell counts or colony-forming units (CFUs).


Methods


The parts listed below are from the 2018 iGEM Distribution Kit and were transformed into chemically competent E. coli DH5-α cells and were used for all cell measurements.


Normalizing fluorescence measurements to absolute cell counts:

E. coli cell concentrations were approximated by comparing the cell absorbance measurements to silica bead absorbance measurements. These silica beads are the same shape and size as an E. coli cell, therefore they scatter and absorb light in a similar way. Given that the bead concentrations were known, each cell absorbance measurement could be converted to a standard "equivalent concentration of beads".


Normalizing to colony-forming units (CFUs):

The number of CFUs grown after liquid media is poured onto a plate is an indication of the number of live cells that were in that media. Using this method with E. coli cells, a conversion factor from absorbance to CFU was computed.


The methods and protocols used for this study were distributed by the iGEM Measurement Committee and can be found here.


Results


Calibration

Before we began cell measurements, standard curves were created from the absorbance readings and fluorescent measurements of silica bead (particle) and fluorescein serial dilutions. This was done to standardize our absorbance readings and fluorescent measurements.

Figure 1. Particle standard curve

Figure 2. Log particle standard curve


Figure 3. Fluorescein standard curve

Figure 4. Log fluorescein standard curve



Cell Measurements


Figure 5. Net Abs600 of each device

Figure 6. Net fluorescein a.u. of each device


Figure 7. uM fluorescein / OD. This graph accounts for the amount of GFP produced and the number of cells present.


Figure 8. MEFL / Particle. This graph accounts for the measure of fluorescence per particle/single cell.