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| − | {{:Team:Manchester/Templates/NavBar}} | + | {{Template:AshesiGhana/NavBar}} |
| | + | {{Template:AshesiGhana/NavBar2}} |
| | {{ManchesterMobile}} | | {{ManchesterMobile}} |
| | <html> | | <html> |
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| | <div class="column full_size"> | | <div class="column full_size"> |
| | | | |
| − | <p>This page shows general protocols given by the suppliers, supervisors or published papers. Visit <a class="linktolabbook" target="_blank" href="https://2017.igem.org/Team:Manchester/Notebook">Lab Book</a> page for detailed experimental procedures (including trials and errors, attempted improvements etc) undergone by us.</p><br> | + | <p>This page shows general protocols given by the suppliers, supervisors and/or published papers. |
| | </div> | | </div> |
| | | | |
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| | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P1-collapse" aria-expanded="false" aria-controls="P1-collapse"> | | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P1-collapse" aria-expanded="false" aria-controls="P1-collapse"> |
| | <div> | | <div> |
| − | <div class="col-md-11"> Chemical Transformation</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div> | + | <div class="col-md-11">Transformation Protocol</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div> |
| | </div> | | </div> |
| | </a> | | </a> |
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| | <div class="panel-body"> | | <div class="panel-body"> |
| | <p> | | <p> |
| − | <b>Materials (consumables):</b><br> | + | <b>Materials </b><br> |
| − | LB broth (Luria Bertrani medium = rich media to grow bacteria)<br>
| + | Resuspended DNA<br> |
| − | TSS buffer (to prepare chemically competent cells)<br>
| + | 10pg/ul Control DNA<br> |
| − | S.O.C. medium (helps obtain the maximal transformation efficiency)<br>
| + | Competent Cells<br> |
| − | LB agar (gel where bacteria can grow)<br> | + | 2ml Microtubes<br> |
| − | Chloramphenicol (CAL) at stock concentration 25mg/ml<br>
| + | Floating Foam Tubes<br> |
| | + | Ice $ Ice Bucket<br> |
| | + | Lab Timer 42 °C water bath<br> |
| | + | SOC Media<br> |
| | + | 37C Incubator<br> |
| | + | Pertri plates w/ LB agar and antibiotic<br> |
| | + | Sterile Spreader<br> |
| | + | Pipettes and Tips<br> |
| | <br> | | <br> |
| | <b>Preparation of chemical competent cells:</b> | | <b>Preparation of chemical competent cells:</b> |
| | <ol style="font-size:16px;"> | | <ol style="font-size:16px;"> |
| − | <li>Inoculate DH5α cells into 50mL LB and incubate at 37°C<br></li> | + | <li>Thaw competent cells on ice<br></li> |
| − | <li>Monitor growth every 30 min by measuring optical density at 600nm (OD600) until it reaches OD600 = 0.4-0.6<br></li> | + | <li>Pipette 50 micto liters of competent cells into 2ml tube<br></li> |
| − | <li>Harvest cells and prepare using 'TSS competent E.coli protocol' shown below:<br></li> | + | <li>Pipette 1 micro litre of resuspended DNA into 2ml tube<br></li> |
| | + | <li>Pipette 1 micro litre of control DNA into 2ml tube<br></li> |
| | + | <li>Close 2ml tubes, incubate on ice for 30min<br></li> |
| | + | <li>Heat shock tubes at 42C for 1 min<br></li> |
| | + | <li>Incubate on ice for 5min<br></li> |
| | </ol> | | </ol> |
| | </p> | | </p> |
| | | | |
| − | <p>
| |
| − | <b>LB Agar plates preparation:</b>
| |
| − | <ol style="font-size:16px;">
| |
| − | <li>Prepare LB containing chloramphenicol (CAL) (at 25μg/ml) <br></li>
| |
| − | <ul style="font-size:16px;">
| |
| − | <li>Melt LB in microwave (defrost setting for 15 min)</li>
| |
| − | <li>Cool LB by running cold water over</li>
| |
| − | <li>Stock of 25mg/ml CAL → so add 400μl CAL to 400ml LB</li>
| |
| − | </ul>
| |
| − | <li>Pour plates (in fume hood) and allow to solidify<br></li>
| |
| − | </ol>
| |
| − | </p>
| |
| | | | |
| | <p> | | <p> |
| | <b>Chemical Transformation:</b> | | <b>Chemical Transformation:</b> |
| | <ol style="font-size:16px;"> | | <ol style="font-size:16px;"> |
| − | <li>Add 1μl of DNA to 50μl of competent cells, mix well and place on ice for at least 30 min <br></li> | + | |
| − | <li>Heat shock cells at 42°C for 30 seconds, followed by 2 min incubation on ice<br></li> | + | <li>Pipette 200microlitre SOC media to each transformation <br></li> |
| − | <li>Add 450μl of SOC medium to the cells and incubate for 45 min at 37°C (to allow protein expression (particularly the antibiotic resistance gene)<br></li> | + | <li>Incubate at 37C for 2 hours, shaker or rotor recommended<br></li> |
| − | <li>Plate and spread (glass spreader sterilised over a flame and in ethanol) 50, 100, and 200μl of the cells into the agar plates made previously<br></li> | + | <li>Pipette each transformation on 2 petri plates for a 20 micro litre and 200 micro litre plating <br></li> |
| − | <li>Incubate at 37°C for 2 hours<br></li> | + | <li>Incubate transformations overnight<br></li> |
| | + | <li>APick single colonies<br></li> |
| | + | <li>Count colonies for control transformation<br></li> |
| | </ol> | | </ol> |
| | </p> | | </p> |
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| | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P2-collapse" aria-expanded="false" aria-controls="P2-collapse"> | | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P2-collapse" aria-expanded="false" aria-controls="P2-collapse"> |
| | <div> | | <div> |
| − | <div class="col-md-11"> TSS Competent E. coli Preparation</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div> | + | <div class="col-md-11"> Plasmid Digest</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div> |
| | </div> | | </div> |
| | </a> | | </a> |
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| | <p> | | <p> |
| | <b>Materials (consumables):</b><br> | | <b>Materials (consumables):</b><br> |
| − | Dimethyl sulfoxide (DMSO)<br>
| + | 5µl NEB buffer 2 <br> |
| − | Polyethylene glycol (PEG)<br>
| + | 0.5µl EcoRI-HF <br> |
| − | MgCl2 stock solution<br>
| + | 0.5µl PstI<br> |
| − | LB or SOC liquid medium<br>
| + | 19µl dH20 <br> |
| | Ice<br> | | Ice<br> |
| | <br> | | <br> |
| | <b>Methods:</b><br> | | <b>Methods:</b><br> |
| | <ol style="font-size:16px;"> | | <ol style="font-size:16px;"> |
| − | <li>Inoculate DH5α E. coli cells into 50ml LB broth and incubate at 37°C</li> | + | <li>Add 4µl linearized plasmid backbone (25ng/µl for 100ng total) </li> |
| − | <li>Prepare the TSS buffer while waiting for the culture to grow and place it on ice (see: Table below)</li>
| + | <li>Add 4µl of Enzyme Master Mix </li> |
| − | <li>Monitor growth of the culture every 30 min by measuring the optical density at 600nm wavelength (OD600) until it reaches OD600 = 0.4-0.6 (takes approximately 2-3 hours)</li> | + | <li>MDigest 37⁰C/30min, heat kill 80⁰C/20min.</li> |
| − | <li>Once the proper optical density has been achieved, take 100ml of culture and centrifuge under 2.700xg for 10 min at 4°C</li> | + | |
| − | <li>Resuspend each tube in 5ml of pre-chilled TSS buffer with gentle vortexing</li>
| + | |
| − | <li>Chill TSS suspended cells on ice for 15 min</li>
| + | |
| − | <li>Aliquot 200μL of TSS suspended cells while ensuring the cells remain well mixed</li>
| + | |
| − | <li>Cells can be used immediately or stored at -80°C</li>
| + | |
| | </ol> | | </ol> |
| | </p> | | </p> |
| | | | |
| − | <p><b>TSS Buffer Composition</b></p>
| |
| − | <table class="table table-bordered table-striped">
| |
| − | <thead>
| |
| − | <tr>
| |
| − | <th>Component</th>
| |
| − | <th>Stock (M)</th>
| |
| − | <th>Amount</th>
| |
| − |
| |
| − | </tr>
| |
| − | </thead>
| |
| − | <tbody>
| |
| − | <tr>
| |
| − | <td>MgCl2</td>
| |
| − | <td>2</td>
| |
| − | <td>0.300ml</td>
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>DMSO</td>
| |
| − | <td>-</td>
| |
| − | <td>1ml</td>
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>PEG (3350 or 8000)</td>
| |
| − | <td>-</td>
| |
| − | <td>2g</td>
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>LB Medium</td>
| |
| − | <td>to final volume of 20ml</td>
| |
| − | <td>to final volume of 20ml</td>
| |
| − | </tr>
| |
| | | | |
| − | </tbody>
| |
| − | </table>
| |
| | | | |
| | </div> | | </div> |
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| | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P3-collapse" aria-expanded="false" aria-controls="P3-collapse"> | | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P3-collapse" aria-expanded="false" aria-controls="P3-collapse"> |
| | <div> | | <div> |
| − | <div class="col-md-11"> PCR From Plasmid DNA Template</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div> | + | <div class="col-md-11"> Part Digest</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div> |
| | </div> | | </div> |
| | </a> | | </a> |
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| | <p> | | <p> |
| | <b>Materials (consumables):</b><br> | | <b>Materials (consumables):</b><br> |
| − | 2x Q5 Master Mix<br>
| + | 5µl NEB Buffer 2 <br> |
| − | 10 µM forward primer<br>
| + | 0.5µl EcoRI-HF<br> |
| − | 10 µM reverse primer<br>
| + | 0.5µL SpeI <br> |
| | DNA template<br> | | DNA template<br> |
| − | Nuclease-free water<br>
| + | 19µl dH2O <br> |
| | <br> | | <br> |
| | <b>Methods:</b><br> | | <b>Methods:</b><br> |
| | <ol style="font-size:16px;"> | | <ol style="font-size:16px;"> |
| − | <li>Gently mix the reaction from the components listed in the table below and place on ice | + | <li>Add 10µl of part DNA (100ng total) </li> |
| − | <br><i>Note: addition of reagents are done in the following order to prevent degradation of primers: nuclease-free water, both primers, DNA, and then Q5 mix</i></li>
| + | <li>Add 4µl of enzyme Mix </li> |
| − | <p><br><b>PCR Reaction Components</b><br>
| + | <li>Digest 37⁰C/30min, heat kill 80⁰C/20min </li> |
| − | <table class="table table-bordered table-striped">
| + | |
| − | <thead>
| + | |
| − | <tr>
| + | |
| − | <th>Component</th>
| + | |
| − | <th>25µl Reaction</th>
| + | |
| − | <th>50µl Reaction</th>
| + | |
| − | <th>Final concentration</th>
| + | |
| − |
| + | |
| − | </tr>
| + | |
| − | </thead>
| + | |
| − | <tbody>
| + | |
| − | <tr>
| + | |
| − | <td>Q5 High-Fidelity 2X Master Mix</td>
| + | |
| − | <td>12.5µl</td>
| + | |
| − | <td>25µl</td>
| + | |
| − | <td>1X</td>
| + | |
| − | </tr>
| + | |
| − | <tr>
| + | |
| − | <td>10µM Forward Primer</td>
| + | |
| − | <td>1.25µl</td>
| + | |
| − | <td>2.5µl</td>
| + | |
| − | <td>0.5µM</td>
| + | |
| − | </tr>
| + | |
| − | <tr>
| + | |
| − | <td>10µM Reverse Primer</td>
| + | |
| − | <td>1.25µl</td>
| + | |
| − | <td>2.5µl</td>
| + | |
| − | <td>0.5µM</td>
| + | |
| − | </tr>
| + | |
| − | <tr>
| + | |
| − | <td>Template DNA</td>
| + | |
| − | <td>variable</td>
| + | |
| − | <td>variable</td>
| + | |
| − | <td>< 1,000ng</td>
| + | |
| − | </tr>
| + | |
| − | <tr>
| + | |
| − | <td>Nuclease-Free Water</td>
| + | |
| − | <td>to 25µl</td>
| + | |
| − | <td>to 50µl</td>
| + | |
| − | <td></td>
| + | |
| − | </tr>
| + | |
| − | | + | |
| − | </tbody>
| + | |
| − | </table>
| + | |
| − | <li>When necessary, collect all liquid to the bottom of the PCR tube by spinning for a short time</li> | + | |
| − | <li>Transfer the PCR tube from ice to a PCR machine and begin thermocycling</li> | + | |
| − | </ol>
| + | |
| − | | + | |
| − | <p><br><b>Thermocycling</b><br>
| + | |
| − | The PCR machine should be set to run the following steps: </p>
| + | |
| − | <table class="table table-bordered table-striped">
| + | |
| − | <thead>
| + | |
| − | <tr>
| + | |
| − | <th>Step</th>
| + | |
| − | <th>Temperature (°C)</th>
| + | |
| − | <th>Time</th>
| + | |
| − |
| + | |
| − | </tr>
| + | |
| − | </thead>
| + | |
| − | <tbody>
| + | |
| − | <tr>
| + | |
| − | <td>Initial denaturation</td>
| + | |
| − | <td>98</td>
| + | |
| − | <td>30 seconds</td>
| + | |
| − | </tr>
| + | |
| − | <tr>
| + | |
| − | <td>30 cycles</td>
| + | |
| − | <td>98 (denaturation)<br>
| + | |
| − | 63 (annealing) <a href="#Note1">see Note 1</a><br>
| + | |
| − | 72 (extension)</td>
| + | |
| − | <td>5 seconds <br>
| + | |
| − | 30 seconds<br>
| + | |
| − | 27 seconds per kb</td>
| + | |
| − | </tr>
| + | |
| − | <tr>
| + | |
| − | <td>Final extension</td>
| + | |
| − | <td>72</td>
| + | |
| − | <td>2 minutes</td>
| + | |
| − | </tr>
| + | |
| − | <tr>
| + | |
| − | <td>Hold</td>
| + | |
| − | <td>10</td>
| + | |
| − | <td>-</td>
| + | |
| − | </tr>
| + | |
| − | | + | |
| − | </tbody>
| + | |
| − | </table>
| + | |
| − | | + | |
| − | <p id="Note1">Note 1: The NEB Tm calculator should be used to determine the annealing temperature when using the Q5 Master Mix: <a target="_blank" href="http://tmcalculator.neb.com/#!/">http://tmcalculator.neb.com/#!/</a></p>
| + | |
| − | | + | |
| − | </p>
| + | |
| | | | |
| | </div> | | </div> |
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| | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P4-collapse" aria-expanded="false" aria-controls="P4-collapse"> | | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P4-collapse" aria-expanded="false" aria-controls="P4-collapse"> |
| | <div> | | <div> |
| − | <div class="col-md-11"> Agarose Gel Electrophoresis</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div> | + | <div class="col-md-11"> LB Agar AND LB Chloramphemicol Plates </div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div> |
| | </div> | | </div> |
| | </a> | | </a> |
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| | <p> | | <p> |
| | <b>Materials (consumables):</b><br> | | <b>Materials (consumables):</b><br> |
| − | 1% TAE Buffer<br>
| + | LB broth <br> |
| − | Agarose powder<br>
| + | Bacteriological Agar <br> |
| − | SYBR Safe<br>
| + | 100mg/ml Chloramphenicol Solution <br> |
| − | Loading dye<br>
| + | |
| − | DNA ladder<br>
| + | |
| | <br> | | <br> |
| − | <b>Make 1% agarose gel:</b><br> | + | <b>PREPARATION OF LB-AGAR PLATE (500ml) </b><br> |
| | <ol style="font-size:16px;"> | | <ol style="font-size:16px;"> |
| − | <li>Prepare 1% TAE agarose gel: dissolve 1g of agarose into 100ml of TAE buffer in a conical flask</li> | + | <li>Add 12.5g of LB broth powder into an appropriate bottle</li> |
| − | <li>Warm in microwave for 1 min at max power</li> | + | <li>Add 7.5g of Agar </li> |
| − | <li>Remove flask from microwave with care, swirl gently and cool under running tap</li> | + | <li>Autoclave </li> |
| − | <li>Add 5µl of SYBR Safe</li> | + | <li>Pour hot/ warm (melted) media at 20ml per petri dish</li> |
| − | <li>Prepare a casting tray with suitable comb</li> | + | </ol> |
| − | <li>Pour to cool mixture into the casting tray and wait 15 min until it solidifies</li> | + | |
| | + | <br> |
| | + | <b>PREPARATION OF LB-AMP PLATE (500ml) </b><br> |
| | + | <ol style="font-size:16px;"> |
| | + | <li>Add 12.5g of LB broth powder into an appropriate bottle 2</li> |
| | + | <li>Add 7.5g of Agar </li> |
| | + | <li>Autoclave </li> |
| | + | <li> Allow media to cool till it can be felt at the back of the palm without burning (but still not solidified). </li> |
| | + | |
| | + | <li> Add 500µl of 100mg/ml Chloramphenicol solution </li> |
| | + | |
| | + | <li> Swirl to mix the antibiotic uniformly in the media </li> |
| | + | <li> Pour the melted media at 20ml per petri dish</li> |
| | </ol> | | </ol> |
| | </p> | | </p> |
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| | </div> | | </div> |
| | | | |
| − | <div class="some-padding"></div>
| |
| − | <div class="some-padding"></div>
| |
| | | | |
| − | <div class="panel-group" id="accordion" role="tablist" aria-multiselectable="true">
| |
| − | <div class="panel panel-default">
| |
| − | <div class="panel-heading" role="tab" id="P5">
| |
| − | <h4 class="panel-title">
| |
| − | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P5-collapse" aria-expanded="false" aria-controls="P5-collapse">
| |
| − | <div>
| |
| − | <div class="col-md-11">Restriction Digestion and Ligation</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div>
| |
| − | </div>
| |
| − |
| |
| − | </a>
| |
| − | </h4>
| |
| − |
| |
| − | </div>
| |
| − | <div id="P5-collapse" class="panel-collapse collapse" role="tabpanel" aria-labelledby="P5">
| |
| − | <div class="panel-body">
| |
| − | <p>
| |
| − | <specialh3>Restriction Digestion</specialh3><br>
| |
| − | <b>Materials (consumables):</b><br>
| |
| − | Restriction Enzyme: <a href"https://www.neb.com/tools-and-resources/interactive-tools/enzyme-finder?searchType=7&recognitionSite=&matchType=1">NEB enzyme finder</a> to determine the restriction enzymes <br>
| |
| − | 10X Buffer: <a href"https://www.neb.com/tools-and-resources/interactive-tools/double-digest-finder">NEB double digest finder</a> to determine the buffers that are required <br>
| |
| − | Plasmid DNA<br>
| |
| − | Nuclease-free water<br>
| |
| − | <br>
| |
| − | <b>Methods:</b><br>
| |
| − | <ol style="font-size:16px;">
| |
| − | <li>Incubate the digestion reaction (see components below) for 1 hour at 37°C, then at 65°C for 20 min (to heat-inactivate the enzymes)</li>
| |
| − | <p><br><b>Restriction Digestion Mix</b><br>
| |
| − | <table class="table table-bordered table-striped">
| |
| − | <thead>
| |
| − | <tr>
| |
| − | <th>Component</th>
| |
| − | <th>50µl Reaction</th>
| |
| − | <th>Final concentration</th>
| |
| − |
| |
| − | </tr>
| |
| − | </thead>
| |
| − | <tbody>
| |
| − | <tr>
| |
| − | <td>10X Buffer</td>
| |
| − | <td>50µl</td>
| |
| − | <td>1X</td>
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>DNA</td>
| |
| − | <td>will vary</td>
| |
| − | <td>250ng</td>
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Restriction Enzymes</td>
| |
| − | <td>1µl (of each enzyme)</td>
| |
| − | <td>10U</td>
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Nuclease-free water</td>
| |
| − | <td>to 50µl</td>
| |
| − | <td> </td>
| |
| − | </tr>
| |
| − | </tbody>
| |
| − | </table>
| |
| − | </ol>
| |
| − | </p>
| |
| − |
| |
| − | <p>
| |
| − | <specialh3>Ligation</specialh3><br>
| |
| − | <b>Materials (consumables):</b><br>
| |
| − | T4 Ligase Buffer<br>
| |
| − | T4 Ligase<br>
| |
| − | Vector DNA<br>
| |
| − | Insert DNA<br>
| |
| − | Nuclease-free water<br>
| |
| − | Ice<br>
| |
| − | <br>
| |
| − | <b>Methods:</b><br>
| |
| − | <ol style="font-size:16px;">
| |
| − | <li>Allow the buffer to defrost on ice</li>
| |
| − | <li>Calculate molar ratio for vector and insert DNA using NEBioCalculator (<a href="http://nebiocalculator.neb.com/#!/ligation">NEBioCalculator</a>) (ideal ratio for insert:vector is 3:1)</li>
| |
| − | <li>Make up ligation reaction as below</li>
| |
| − | <ul style="font-size:16px;">
| |
| − | <li>If using T4 ligase: incubate at room temp for 1 hour</li>
| |
| − | <li>NB: different ligases (eg. Quick Ligase) will require different incubation times</li>
| |
| − | </ul>
| |
| − | <p><br><b>Ligation Reaction Composition</b><br>
| |
| − | <table class="table table-bordered table-striped">
| |
| − | <thead>
| |
| − | <tr>
| |
| − | <th>Component</th>
| |
| − | <th>10µl Reaction</th>
| |
| − | <th>Final concentration</th>
| |
| − |
| |
| − | </tr>
| |
| − | </thead>
| |
| − | <tbody>
| |
| − | <tr>
| |
| − | <td>10X T4 Ligase Buffer</td>
| |
| − | <td>1µl</td>
| |
| − | <td>1X</td>
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Vecor DNA</td>
| |
| − | <td>vary</td>
| |
| − | <td> </td>
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Insert DNA</td>
| |
| − | <td>vary</td>
| |
| − | <td> </td>
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Nuclease-free water</td>
| |
| − | <td>to 10µl</td>
| |
| − | <td> </td>
| |
| − | </tr>
| |
| − |
| |
| − | </tbody>
| |
| − | </table>
| |
| − | </ol>
| |
| − | </p>
| |
| − |
| |
| − | </div>
| |
| − | </div>
| |
| − | </div>
| |
| − |
| |
| − | <div class="some-padding"></div>
| |
| − | <div class="some-padding"></div>
| |
| − |
| |
| − | <div class="panel-group" id="accordion" role="tablist" aria-multiselectable="true">
| |
| − | <div class="panel panel-default">
| |
| − | <div class="panel-heading" role="tab" id="P6">
| |
| − | <h4 class="panel-title">
| |
| − | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P6-collapse" aria-expanded="false" aria-controls="P6-collapse">
| |
| − | <div>
| |
| − | <div class="col-md-11">PCR Purification (QIAquick PCR Purification Kit)</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div>
| |
| − | </div>
| |
| − | </a>
| |
| − | </h4>
| |
| − |
| |
| − | </div>
| |
| − | <div id="P6-collapse" class="panel-collapse collapse" role="tabpanel" aria-labelledby="P6">
| |
| − | <div class="panel-body">
| |
| − |
| |
| − | <p>
| |
| − | <b>Materials (consumables):</b><br>
| |
| − | Ethanol (96-100%)<br>
| |
| − | Buffer PE<br>
| |
| − | Buffer PB<br>
| |
| − | Buffer EB<br>
| |
| − | pH indicator I<br>
| |
| − | Sodium acetate<br>
| |
| − | QIAquick column<br>
| |
| − | Loading dye<br>
| |
| − | <br>
| |
| − | <b>Notes before starting:</b><br>
| |
| − | <ol style="font-size:16px;">
| |
| − | <li>Add ethanol (96-100%) to buffer PE before use (see bottle label for volume)</li>
| |
| − | <li>All centrifugation steps are carried out at 17,900 x g (13,000 rpm) in a conventional table-top microcentrifuge at room temperature</li>
| |
| − | <li>Add 1:250 volume pH indicator I to Buffer PB. The yellow color of Buffer PB with pH indicator I indicates a pH of ≤7.5. If the purified PCR product is to be used in sensitive microarray applications, it may be beneficial to use Buffer PB without the addition of pH indicator I. Do not add pH indicator I to buffer aliquots</li>
| |
| − | </ol>
| |
| − | </p>
| |
| − |
| |
| − | <p>
| |
| − | <b>Methods:</b><br>
| |
| − | <ol style="font-size:16px;">
| |
| − | <li>Add 5 volumes Buffer PB to 1 volume of the PCR reaction and mix. If the color of the mixture is orange or violet, add 10μl 3M sodium acetate, pH 5.0, and mix. The color of the mixture will turn yellow</li>
| |
| − | <li>Place a QIAquick column in a provided 2 ml collection tube</li>
| |
| − | <li>To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 seconds until all the samples have passed through the column. Discard flow-through and place the QIAquick column back in the same tube</li>
| |
| − | <li>To wash, add 0.75ml Buffer PE to the QIAquick column and centrifuge for 30–60 seconds. Discard flow-through and place the QIAquick column back in the same tube</li>
| |
| − | <li>Centrifuge the QIAquick column once more in the provided 2ml collection tube for 1 min to remove residual wash buffer</li>
| |
| − | <li>Place each QIAquick column in a clean 1.5ml microcentrifuge tube</li>
| |
| − | <li>To elute DNA, add 50μl Buffer EB (10 mM Tris·Cl, pH 8.5) or water (pH 7.0–8.5) to the center of the QIAquick membrane and centrifuge the column for 1 min. For increased DNA concentration, add 30μl elution buffer to the center of the QIAquick membrane, let the column stand for 1 min, and then centrifuge</li>
| |
| − | <li>If the purified DNA is to be analyzed on a gel, add 1 volume of Loading dye to 5 volumes of purified DNA. Mix the solution by pipetting up and down before loading the gel</li>
| |
| − | </ol>
| |
| − | </p>
| |
| − |
| |
| − | </div>
| |
| − | </div>
| |
| − | </div>
| |
| | | | |
| | <div class="some-padding"></div> | | <div class="some-padding"></div> |
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| | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P8-collapse" aria-expanded="false" aria-controls="P8-collapse"> | | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P8-collapse" aria-expanded="false" aria-controls="P8-collapse"> |
| | <div> | | <div> |
| − | <div class="col-md-11">Miniprep (QIAprep Spin Miniprep Kit)</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div> | + | <div class="col-md-11"> |
| | + | Zyppy™ Plasmid Miniprep</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div> |
| | </div> | | </div> |
| | </a> | | </a> |
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| | <p> | | <p> |
| | <b>Materials (consumables):</b><br> | | <b>Materials (consumables):</b><br> |
| − | Overnight culture<br>
| + | 7X Lysis Buffer*1 (Blue) <br> |
| − | Buffer P1<br> | + | Neutralization Buffer*2 (Yellow) <br> |
| − | Buffer P2<br> | + | Endo-Wash Buffer <br> |
| − | Buffer N3<br> | + | Zyppy™ Elution Buffer <br> |
| − | Buffer PE<br> | + | Collection Tubes<br> |
| − | Sterile dH2O (MiliQ) water<br>
| + | |
| | <br> | | <br> |
| | <b>Methods:</b><br> | | <b>Methods:</b><br> |
| | <ol style="font-size:16px;"> | | <ol style="font-size:16px;"> |
| − | <li>Spin down the overnight cultures at 10000rpm for 10 min. Discard supernatant into virkon</li> | + | <li>Add 600 µl of bacterial culture grown in LB medium to a 1.5 ml microcentrifuge tube. </li> |
| − | <li>Resuspend the pelleted bacteria with 250μl of Buffer P1 (stored in fridge), and transfer the resuspended bacteria into a fresh 2ml eppendorf </li>
| + | <li>Add 100 µl of 7X Lysis Buffer (Blue)1 and mix by inverting the tube 4-6 times. Proceed to step 3 within 2 minutes. </li> |
| − | <li>Add 250μl of Buffer P2 to the 2mL Eppendorf with bacteria and mix gently. Sample should turn blue (indicates cells have lysed)</li> | + | <li>Add 350 µl of cold Neutralization Buffer (Yellow) and mix thoroughly</li> |
| − | <li>Incubate for 5 min at room temperature (do not exceed 5 min or plasmid will begin to degrade)</li>
| + | <li>Place the column into a Collection Tube and centrifuge for 15 seconds. </li> |
| − | <li>Add 350μl of Buffer N3 and mix gently. Sample should be colourless and contain a white precipitant</li> | + | <li>Discard the flow-through and place the column back into the same Collection Tube. </li> |
| − | <li>Centrifuge samples at 14,000rpm for 10 min using a table top centrifuge</li> | + | <li>Add 200 µl of Endo-Wash Buffer to the column</li> |
| − | <li>Transfer 750μl of the supernatant to a column placed on a 1.5ml Eppendorf tube (discard white precipitate). Centrifuge at 11,000rpm for 1 min using a table top centrifuge</li> | + | <li>Add 400 µl of Zyppy™ Wash Buffer to the column</li> |
| − | <li>Discard the flow-through. Place column onto new eppendorf tube and add 750μl PE buffer (with added ethanol to the stock buffer if not already done so). Incubate at room temperature for 5 min. Centrifuge at 13,000rpm for 30 seconds</li> | + | <li> Transfer the column into a clean 1.5 ml microcentrifuge tube then add 30 µl of Zyppy™ Elution Buffer2 directly to the column matrix and let stand for one minute at room temperature. |
| − | <li>Transfer column to fresh eppendorf. Centrifuge at 13,000rpm for 2 min (dry out)</li> | + | </li> |
| − | <li>Transfer column into fresh eppendorf. Add 30μl of sterile dH20 (MiliQ) (add directly onto column to ensure water pushes DNA through) and incubate for 5 min at room temperature</li> | + | <li>. Centrifuge for 30 seconds to elute the plasmid DNA. </li> |
| − | <li>Centrifuge at 11,000rpm for 1 min. <b>Do not discard this flow-through</b>. This contains the extracted plasmid | + | |
| − | </ol> | + | |
| | | | |
| − | </div>
| |
| − | </div>
| |
| − | </div>
| |
| − |
| |
| − | <div class="some-padding"></div>
| |
| − | <div class="some-padding"></div>
| |
| − |
| |
| − |
| |
| − | <div class="panel-group" id="accordion" role="tablist" aria-multiselectable="true">
| |
| − | <div class="panel panel-default">
| |
| − | <div class="panel-heading" role="tab" id="P7">
| |
| − | <h4 class="panel-title">
| |
| − | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P7-collapse" aria-expanded="false" aria-controls="P7-collapse">
| |
| − | <div>
| |
| − | <div class="col-md-11">Gel Extraction (QIAgen Gel Extraction Kit)</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div>
| |
| − | </div>
| |
| − | </a>
| |
| − | </h4>
| |
| − |
| |
| − | </div>
| |
| − | <div id="P7-collapse" class="panel-collapse collapse" role="tabpanel" aria-labelledby="P7">
| |
| − | <div class="panel-body">
| |
| − | <p>
| |
| − | <b>Materials (consumables):</b><br>
| |
| − | Buffer QG<br>
| |
| − | Buffer PE<br>
| |
| − | Buffer PB<br>
| |
| − | 3M Sodium Acetate<br>
| |
| − | Sterile dH2O (MiliQ) water<br>
| |
| − | Isopropanol<br>
| |
| − | <br>
| |
| − | <b>Methods:</b><br>
| |
| − | <ol style="font-size:16px;">
| |
| − | <li>Excise the DNA fragment from the agarose gel with a clean, sharp scalpel</li>
| |
| − | <li>Weigh the gel slice in a colorless tube. Add 3 volumes Buffer QG to 1 volume gel (100mg gel ~ 100μl). The maximum amount of gel per spin column is 400mg. For >2% agarose gels, add 6 volumes Buffer QG</li>
| |
| − | <li>Incubate at 50°C for 10 min (or until the gel slice has completely dissolved). Vortex the tube every 2–3 min to help dissolve gel. After the gel slice has dissolved completely, check that the color of the mixture is yellow (similar to Buffer QG without dissolved agarose). If the color of the mixture is orange or violet, add 10μl 3 M sodium acetate, pH 5.0, and mix. The mixture turns yellow</li>
| |
| − | <li>Add 1 gel volume isopropanol to the sample and mix</li>
| |
| − | <li>Transfer 750µl of supernatant to a column placed on a 1.5ml eppendorf. Centrifuge at 11,000 rpm for 1 min</li>
| |
| − | <li>Discard flow through. Place column in a new Eppendorf tube. Add 500µl of PB buffer and centrifuge column at 13,000 rpm for 30 seconds</li>
| |
| − | <li>Discard flow through. Place column in a new eppendorf. Add 750µl of PE buffer (check ethanol has been added, see: PCR Purification). Incubate at room temp for 5 mins, then centrifuge at 13,000 rpm for 30 seconds</li>
| |
| − | <li>Transfer column into fresh Eppendorf. Centrifuge at 13,000 rpm for 2 mins</li>
| |
| − | <li>Transfer column to new eppendorf. Add 30µl of MiliQ water and incubate for 5 mins at room temperature</li>
| |
| − | <li>Final centrifuge at 11,000 rpm for 1 minute</li>
| |
| − | <li>Test sample using Nanodrop (see below)</li>
| |
| | </ol> | | </ol> |
| − | </p>
| |
| − |
| |
| − | <p>
| |
| − | <b>Nanodrop:</b> <i>calculate DNA concentration in sample</i><br>
| |
| − | <ol style="font-size:16px;">
| |
| − | <li>Load 1μL of MiliQ water to the Nanodrop and blank. Clean and load another 1μl of MiliQ water, measure and proceed only if clean (absorbance is zero at all measured wavelengths)</li>
| |
| − | <li>Load 1μl of sample and measure DNA concentration</li>
| |
| − | <li>Check A260/280 ~ 1.8 and A260/230 ~2.0 (pure DNA sample should have values close to these numbers)</li>
| |
| − | </ol>
| |
| − | </p>
| |
| − | </p>
| |
| | | | |
| | </div> | | </div> |
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| | <div class="some-padding"></div> | | <div class="some-padding"></div> |
| − |
| |
| − | <div class="panel-group" id="accordion" role="tablist" aria-multiselectable="true">
| |
| − | <div class="panel panel-default">
| |
| − | <div class="panel-heading" role="tab" id="P9">
| |
| − | <h4 class="panel-title">
| |
| − | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P9-collapse" aria-expanded="false" aria-controls="P9-collapse">
| |
| − | <div>
| |
| − | <div class="col-md-11">LacUV5, Tet and araBad Promoter induction</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div>
| |
| − | </div>
| |
| − | </a>
| |
| − | </h4>
| |
| − |
| |
| − | </div>
| |
| − | <div id="P9-collapse" class="panel-collapse collapse" role="tabpanel" aria-labelledby="P9">
| |
| − | <div class="panel-body">
| |
| − | <p>
| |
| − | <b>Materials (consumables):</b><br>
| |
| − | LB liquid medium<br>
| |
| − | Chloramphenicol at stock concentration of 25mg/ml<br>
| |
| − | IPTG at stock concentration of 100mM<br>
| |
| − | Tetracycline at stock concentration of 0.214mM<br>
| |
| − | Arabinose at stock concentration of 100nM<br>
| |
| − | <br>
| |
| − | <b>Method:</b><br>
| |
| − | Aseptic technique maintained at all times <br>
| |
| − | <br>
| |
| − | <ol style="font-size:16px;">
| |
| − | <li>Transfer 50mL of LB +250L of chloramphenicol into 8x 250mL conical flasks.</li>
| |
| − | <li> Inoculate 2 flasks labelled + and - with 200L of pSBC13eutS overnight culture. </li>
| |
| − | <li>Grow the cultures at 37C in shaking incubator until and OD value of 0.5 is reached. </li>
| |
| − | <li>Add IPTG, Tetracycline and Arabinose to the respective constructs in the amounts
| |
| − | shown below. </li>
| |
| − | <br>
| |
| − | <p><br><b>Inducers to be added to Eut constructs</b><br>
| |
| − | <table class="table table-bordered table-striped">
| |
| − | <thead>
| |
| − | <tr>
| |
| − | <th>Flask</th>
| |
| − | <th>Construct</th>
| |
| − | <th>Inducer and concentration to be added</th>
| |
| − |
| |
| − | </tr>
| |
| − | </thead>
| |
| − | <tbody>
| |
| − | <tr>
| |
| − | <td>Flask 1</td>
| |
| − | <td>pSBC13eutS-</td>
| |
| − | <td>None</td>
| |
| − |
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Flask 2</td>
| |
| − | <td>pSBC13eutS+</td>
| |
| − | <td>250µM IPTG</td>
| |
| − |
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Flask 3</td>
| |
| − | <td>pSBC13eutMN-</td>
| |
| − | <td>None</td>
| |
| − |
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Flask 4</td>
| |
| − | <td>pSBC13eutMN+</td>
| |
| − | <td>1000 nM tetracycline</td>
| |
| − |
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Flask 5</td>
| |
| − | <td>pSBC13eutSMN-</td>
| |
| − | <td>None</td>
| |
| − |
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Flask 6</td>
| |
| − | <td>pSBC13eutSMN+</td>
| |
| − | <td>250µM IPTG and 100nM tetracycline</td>
| |
| − |
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Flask 7</td>
| |
| − | <td>pSBC13eutLK-</td>
| |
| − | <td>None</td>
| |
| − |
| |
| − | </tr>
| |
| − | <tr>
| |
| − | <td>Flask 8</td>
| |
| − | <td>pSBC13eutLK+</td>
| |
| − | <td>500µL arabinose</td>
| |
| − | <td></td>
| |
| − | </tr>
| |
| − |
| |
| − | </tbody>
| |
| − | </table>
| |
| − | <li>Incubate samples for 4hours in a 20C shaking incubator, remove 25mL of the culture and transfer to a falcon tube. </li>
| |
| − | <li>Centrifuge at 9000rpm for 8minutes.</li>
| |
| − | <li>Pour off supernatant, sample can be used immediately or frozen at -20C.</li>
| |
| − | <li>Incubate samples for a further 16 hours at 20C (20 hours in total), transfer culture to a falcon tube.</li>
| |
| − | <li>Centrifuge at 9000rpm for 8minutes.</li>
| |
| − | <li>Pour off supernatant, sample can be used immediately or frozen at -20C.</li>
| |
| − |
| |
| − | </ol>
| |
| − |
| |
| − | </p>
| |
| − |
| |
| − | </div>
| |
| − | </div>
| |
| − | </div>
| |
| | | | |
| | | | |
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| | | | |
| − | <div class="panel-group" id="accordion" role="tablist" aria-multiselectable="true">
| |
| − | <div class="panel panel-default">
| |
| − | <div class="panel-heading" role="tab" id="P10">
| |
| − | <h4 class="panel-title">
| |
| − | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P10-collapse" aria-expanded="false" aria-controls="P10-collapse">
| |
| − | <div>
| |
| − | <div class="col-md-11">Western Blot (for protein expression analysis)Fima</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div>
| |
| − | </div>
| |
| − | </a>
| |
| − | </h4>
| |
| − |
| |
| − | </div>
| |
| − | <div id="P10-collapse" class="panel-collapse collapse" role="tabpanel" aria-labelledby="P10">
| |
| − | <div class="panel-body">
| |
| − | <p>
| |
| − | Protocols.
| |
| − | </p>
| |
| − | </div>
| |
| − | </div>
| |
| − | </div>
| |
| − |
| |
| − |
| |
| − | <div class="some-padding"></div>
| |
| − | <div class="some-padding"></div>
| |
| − |
| |
| − | <div class="panel-group" id="accordion" role="tablist" aria-multiselectable="true">
| |
| − | <div class="panel panel-default">
| |
| − | <div class="panel-heading" role="tab" id="P11">
| |
| − | <h4 class="panel-title">
| |
| − | <a role="button" class="collapsed" data-toggle="collapse" data-parent="#accordion" href="#P11-collapse" aria-expanded="false" aria-controls="P11-collapse">
| |
| − | <div>
| |
| − | <div class="col-md-11">Cell Fixation (using paraformaldehyde)</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div>
| |
| − | </div>
| |
| − | </a>
| |
| − | </h4>
| |
| − |
| |
| − | </div>
| |
| − | <div id="P11-collapse" class="panel-collapse collapse" role="tabpanel" aria-labelledby="P11">
| |
| − | <div class="panel-body">
| |
| − | <p>
| |
| − | <b>Materials (consumables):</b><br>
| |
| − | Phosphate Buffered Saline (PBS)<br>
| |
| − | PBS + 2% paraformaldehyde
| |
| − | <br>
| |
| − | <br>
| |
| − | <b>Method:</b><br>
| |
| − | <ol style="font-size:16px;">
| |
| − | <li>Using a fresh transformation plate prepare overnights as follows:<br>
| |
| − | 10ml LB<br>
| |
| − | 10μl of each antibiotic as required (Chloramphenicol for localization tags and Ampicillin for Eut)<br>
| |
| − | Inoculate media with a single colony<br>
| |
| − | Grow overnight at 37⁰C<br></li>
| |
| − | <li>Prepare fresh liquid cultures as follows:<br>
| |
| − | 10ml LB<br>
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| − | 10μl of each antibiotic as required<br>
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| − | Inoculate with 200μl of overnight culture<br></li>
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| − | <li>Grow to OD600 of 0.1, or for roughly 1 hour and induce the whole liquid culture with IPTG, Tet and/or Arabinose as required (IPTG for EutS, Tet for MN & Ara for LK. Tags are constitutive and don't need inducing).<br>
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| − | Add 10μl of 100mM IPTG for 100μM, 2.34μl of 214μM Tet for 50nM & 10μl of 100mM Ara for 100μM.<br></li>
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| − | <li>Incubate induced samples at 30⁰C and take out at desired time-points (I found 2 and 3 hours are sufficient).<br></li>
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| − | <li>At each time-point remove 1ml of each liquid culture and place in 1.5ml eppendorfs.<br>
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| − | Spin down at 5000rpm for 2 minutes in a table top centrifuge and discard supernatant.<br></li>
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| − | <li>Resuspend pellet in 1ml PBS and spin down again at 5000rpm for 2 minutes, discarding supernatant.<br></li>
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| − | <li>Next resuspend pellet in PBS+2% paraformaldehyde and leave at room temperature for 30 minutes.<br></li>
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| − | <li>After 30 minutes, spin down at 5000rpm for 2 minutes and discard supernatant and resuspend pellet in 100μl of PBS.<br></li>
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| − | <br>
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| − | -This suspension is now ready to make slides with.<br>
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| − | <br>
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| − | <div>
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| − | <div class="col-md-11">Preparing Microscope Slides</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div>
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| − | <p>
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| − | <b>Materials (consumables):</b><br>
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| − | Fixed cell suspension<br>
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| − | Blank microscope slides<br>
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| − | Cover slips<br>
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| − | <br>
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| − | <b>Method:</b><br>
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| − | <ol style="font-size:16px;">
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| − | <li>Pipette 12μl of suspension to a slide and add a cover slip.</li>
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| − | <li>Press cover slip down slightly (this helps put all cells in the same plane so it's easier to focus the microscope).</li>
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| − | <li>Allow to dry out of direct light to avoid photo bleaching (under blue roll is sufficient).</li>
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| − | <li>Store somewhere dark like a slide box or wrapped in lens cloth.</li>
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| − | <br>
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| − | -These slides are now ready to be visualized with fluorescence microscopy.<br>
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| − | <h4 class="panel-title">
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| − | <div>
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| − | <div class="col-md-11">Image Analysis (CellProfiler)</div><div class="col-md-1"><i class="fa" aria-hidden="true"></i></div>
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| − | <b>Analysis Modules:</b><br>
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| − | ApplyThreshold<br>
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| − | IdentifyPrimaryObjects<br>
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| − | IdentifyPrimaryObjects<br>
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| − | MeasureObjectSizeShape<br>
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| − | ExportToSpreadsheet<br>
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| − | <br>
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| − | <b>Method:</b><br>
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| − | <ol style="font-size:16px;">
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| − | -(This protocol is meant to inform CellProfiler users of our method of image analysis, not teach users how to use the software. For tutorials on how to use CellProfiler, visit: <a target="_blank" href="http://cellprofiler.org/examples/">http://cellprofiler.org/examples/</a> or <a target="_blank" href="http://cellprofiler.org/tutorials/">http://cellprofiler.org/tutorials/</a>)<br>
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| − | <br>
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| − | <li>Select the ‘Images’ option in the ‘Input modules’ window and drag and drop the target image into the file list.<br></li>
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| − | <li>Select ‘NamesAndTypes’ in the ‘Input modules’ window and enter a value in the ‘Name to assign these images’ box, e.g. “raw_data” and click update.<br></li>
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| − | <li>Right click in the ‘Analysis modules’ window and navigate to Add>All>ApplyThreshold. This will filter out any background noise. From the ‘Select the input image’ drop-down menu, select “raw_data” and name the output image, e.g. “ThreshGreen”. The threshold will need to be tweaked to match the picture, so set the ‘Threshold strategy’ to Manual and change the ‘Manual threshold’ value to match your image (the results can be previewed by clicking the ‘Start Test Mode’ button in the bottom left and using the ‘Step’ button to step through Analysis modules).<br></li>
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| − | <li>Add another module by navigating Add>All>IdentifyPrimaryObjects. Select input as your threshold image e.g. ThreshGreen and name the objects to be identified e.g. Cells. Tweak the typical diameter range of the objects to roughly match your target objects. Select ‘Yes’ to discard objects outside the diameter range and select ‘No’ to discard objects touching the border. Like before set the threshold strategy to manual and tweak to match your image (Use Start Test Mode>Step to preview results to get the optimum identification).<br></li>
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| − | <li>Add another IdentifyPrimaryObjects module, this time for identification of microcompartments. Change the name of the primary objects e.g. Microcompartments, keep settings the same as the previous step but change the typical diameter and threshold values to match the smaller, brighter objects.<br></li>
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| − | <li>Add another module by navigating Add>All>MeasureObjectSizeShape. In ‘select object to measure’ select Cells. Click ‘Add another object’ and select Microcompartments.<br></li>
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| − | <li>Add another module by navigating Add>All>ExportToSpreadsheet. Select column delimiter as “Tab” and select ‘output file location’ as ‘default output folder’ (make sure to set this correctly by clicking ‘view output settings’ and selecting the preferred output folder). Set the ‘Filename prefix’ e.g. “MyExpt_”. Select ‘Yes’ to ‘Select the measurements to export’ and press the button to select measurements. Here you can select which data you want to be exported, in the case of determining circularity of microcompartments, navigate All>Microcompartments>AreaShape>Eccentricity and tick, and also tick All>Microcompartments>Number. In this example an Excel file will be generated with data about circularity of microcompartments which allows them to be ranked by how properly they have formed.<br></li>
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| − | <li>After all modules have been configured and a default output folder selected, click on ‘Analyze Images’ to perform analysis and output data.<br></li>
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| − | <br>
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| − | -This covers the analysis modules for this simple protocol but a more in-depth, custom analysis of data is possible. Different data can be exported to excel, correlation of different fluorescence tags can be analysed, and images with object outlines can be exported (see links above).<br>
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| − | </ol>
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| − | </p>
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