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| html代码不在乎多个空格,仅显示一个 | | html代码不在乎多个空格,仅显示一个 |
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− | <h1>2020 Fudan Protocols(链接需修改)</h1> | + | <h1 tabIndex="1">2020 Fudan Protocols</h1> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Click<a target="_blank" href="https://static.igem.org/mediawiki/2020/b/b7/T--Fudan--Notebook_July.pdf">here</a>to download pdf version version protocols of 2020 Fudan team. </p> | + | <p>Click <a target="_blank" href="https://static.igem.org/mediawiki/2020/0/0a/T--Fudan--Protocol.pdf">here</a> to download the protocols used by 2020 Fudan team, as a single PDF file.</p> |
− | </div> | + | </div> <div class="clear"></div> |
| | | |
| | | |
| <h2>Cell Cryopreservation</h2> | | <h2>Cell Cryopreservation</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Cryopreservation is a technique that store cells at a very low temperatures (-80℃) to reduce cell metabolic damage and enable long-term storage.</p> | + | <p>Cryopreservation is a technique that store cells at a very low temperatures (-80℃) to reduce cell metabolic damage and enable long-term storage.</p> |
| <ol> | | <ol> |
− | <li>Add cryoprotectant: Add 80% glycerin 500μL and bacterial fluid 1 000μL into Cryopreservation vials. Mix upside down gently.</li> | + | <li>Add cryoprotectant: Add 80% glycerin 500 μL and bacterial fluid 1 000 μL into Cryopreservation vials. Mix upside down gently.</li> |
| <li>Seal the vials: Stick sellotape around the label.</li> | | <li>Seal the vials: Stick sellotape around the label.</li> |
| <li>Store the vials: Store prepared vials in refrigerator at -80℃.</li> | | <li>Store the vials: Store prepared vials in refrigerator at -80℃.</li> |
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| <h2>Cell Recovery</h2> | | <h2>Cell Recovery</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Bacteria preserved at -80 ℃ need to be recovery to restores cell growth.</p> | + | <p>Bacteria preserved at -80℃ need to be recovery to restores cell growth.</p> |
| <ol> | | <ol> |
| <li>Prepare plate: Take out the plate with relevant resistance from 4 degrees and wait for the temperature to the room temperature. Mark at the bottom of the plate.</li> | | <li>Prepare plate: Take out the plate with relevant resistance from 4 degrees and wait for the temperature to the room temperature. Mark at the bottom of the plate.</li> |
− | <li>Recover the cell: The -80 ° C frozen strain was removed and placed on the ice quickly. Take a ring of the upper layer of melt bacteria liquid by the sterilized inoculation ring. Coated the plate and draw a line. </li> | + | <li>Recover the cell: The -80℃ frozen strain was removed and placed on the ice quickly. Take a ring of the upper layer of melt bacteria liquid by the sterilized inoculation ring. Coated the plate and draw a line. </li> |
− | <li>Culture the recovered cell: Incubate at 37 degrees overnight.</li> | + | <li>Culture the recovered cell: Incubate at 37℃ overnight.</li> |
| </ol> | | </ol> |
| </div> | | </div> |
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| <p>PCR is performed for amplify DNA fragments in our project.</p> | | <p>PCR is performed for amplify DNA fragments in our project.</p> |
| | | |
− |
| + | |
| <ol> | | <ol> |
− | <li>Set up PCR system (25 µl): | + | <li>Set up PCR system (25 μL): |
− | <table> | + | <table style="font-size:80%;padding:5px;margin:5px"> |
| <tr> | | <tr> |
| <th>Reagent</th> <th>Volume</th> | | <th>Reagent</th> <th>Volume</th> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>ddH2O</td> <td>To 25 µl </td> | + | <td>ddH<sub>2</sub>O</td> <td>To 25 μL </td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>2 x Phanta Max Buffer</td> <td>12.5 µl</td> | + | <td>2 x Phanta Max Buffer</td> <td>12.5 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>dNTP</td> <td>0.5 µl</td> | + | <td>dNTP</td> <td>0.5 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Phanta</td> <td>0.5 µl</td> | + | <td>Phanta</td> <td>0.5 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Template</td> <td><br/>Plasmid: 0.5 µl<br/><br/>PCR product: 1 µl<br/> | + | <td>Template</td> <td><br/>Plasmid: 0.5 μL<br/><br/>PCR product: 1 μL<br/> |
| </td> | | </td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Forward Primer</td> <td>1 µl</td> | + | <td>Forward Primer</td> <td>1 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Reverse Primer</td> <td>1 µl</td> | + | <td>Reverse Primer</td> <td>1 μL</td> |
| </tr> | | </tr> |
| </table></li> | | </table></li> |
| <li>Place the PCR tubes in a PCR amplifier.</li> | | <li>Place the PCR tubes in a PCR amplifier.</li> |
| <li>Set up reaction program: | | <li>Set up reaction program: |
− | <table> | + | <table style="font-size:80%;padding:5px;margin:5px"> |
| <tr> | | <tr> |
| <th>Procedure</th> <th>Temperature</th><th>Time</th><th>Cycle</th> | | <th>Procedure</th> <th>Temperature</th><th>Time</th><th>Cycle</th> |
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| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Final elongation</td> <td>72℃</td><td>5min</td><td>1</td> | + | <td>Final elongation</td><td>72℃</td><td>5min</td><td>1</td> |
| </tr> | | </tr> |
| </table> | | </table> |
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| <p>Colony PCR is performed to determine whether we insert DNA into plasmid successfully.</p> | | <p>Colony PCR is performed to determine whether we insert DNA into plasmid successfully.</p> |
| | | |
− |
| + | |
| <ol> | | <ol> |
| <li>Set up colony PCR system (10 µl): | | <li>Set up colony PCR system (10 µl): |
− | <table> | + | <table style="font-size:80%;padding:5px;margin:5px"> |
| <tr> | | <tr> |
| <th>Reagent</th> <th>Volume</th> | | <th>Reagent</th> <th>Volume</th> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>ddH2O</td> <td>To 10 µl </td> | + | <td>ddH<sub>2</sub>O</td> <td>To 10 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>10 x Taq Buffer</td> <td>1 µl</td> | + | <td>10 x Taq Buffer</td> <td>1 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>dNTP</td> <td>0.2 µl</td> | + | <td>dNTP</td> <td>0.2 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Taq DNA Polymerase</td> <td>0.2 µl</td> | + | <td>Taq DNA Polymerase</td> <td>0.2 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Colony Template</td> <td>1 µl</td> | + | <td>Colony Template</td> <td>1 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Forward Primer</td> <td>0.4 µl</td> | + | <td>Forward Primer</td> <td>0.4 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Reverse Primer</td> <td>0.4 µl</td> | + | <td>Reverse Primer</td> <td>0.4 μL</td> |
| </tr> | | </tr> |
| </table></li> | | </table></li> |
| <li>Place the PCR tubes in a PCR amplifier.</li> | | <li>Place the PCR tubes in a PCR amplifier.</li> |
| <li>Set up reaction program: | | <li>Set up reaction program: |
− | <table> | + | <table style="font-size:80%;padding:5px;margin:5px"> |
| <tr> | | <tr> |
| <th>Procedure</th> <th>Temperature</th><th>Time</th><th>Cycle</th> | | <th>Procedure</th> <th>Temperature</th><th>Time</th><th>Cycle</th> |
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| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Final elongation</td> <td>72℃</td><td>7min</td><td>1</td> | + | <td>Final elongation</td><td>72℃</td><td>7min</td><td>1</td> |
| </tr> | | </tr> |
| </table> | | </table> |
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| <h2>Overlap Extension PCR (OE PCR)</h2> | | <h2>Overlap Extension PCR (OE PCR)</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>OE PCR is used to fuse fragments together.</p> | + | <p>OE PCR is used to fuse fragments together.</p> |
| <ol> | | <ol> |
− | <li> First round PCR: Use primer a/b to amplify fragment AB by PCR, and c/d to amplify fragment CD. Set up PCR system: | + | <li>First round PCR: Use primer a/b to amplify fragment AB by PCR, and c/d to amplify fragment CD. Set up PCR system: |
− | <table> | + | <table style="font-size:80%;padding:5px;margin:5px"> |
| <tr> | | <tr> |
| <th>Reagent</th> <th>Volume</th> | | <th>Reagent</th> <th>Volume</th> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>ddH2O</td> <td>To 25 µl </td> | + | <td>ddH<sub>2</sub>O</td> <td>To 25 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>2 x Phanta Max Buffer</td> <td>12.5 µl</td> | + | <td>2 x Phanta Max Buffer</td> <td>12.5 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>dNTP</td> <td>0.5 µl</td> | + | <td>dNTP</td> <td>0.5 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Phanta</td> <td>0.5 µl</td> | + | <td>Phanta</td> <td>0.5 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Template</td> <td><br/>Plasmid: 0.5 µl<br/><br/>PCR product: 1 µl<br/></td> | + | <td>Template</td> <td>Plasmid: 0.5 μL<br/>PCR product: 1 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Forward Primer</td> <td>1 µl</td> | + | <td>Forward Primer</td> <td>1 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Reverse Primer</td> <td>1 µl</td> | + | <td>Reverse Primer</td> <td>1 μL</td> |
| </tr> | | </tr> |
| </table> | | </table> |
| Set up reaction program: | | Set up reaction program: |
− | <table> | + | <table style="font-size:80%;padding:5px;margin:5px"> |
| <tr> | | <tr> |
| <th>Procedure</th> <th>Temperature</th><th>Time</th><th>Cycle</th> | | <th>Procedure</th> <th>Temperature</th><th>Time</th><th>Cycle</th> |
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| </table> | | </table> |
| </li> | | </li> |
− | <li>Annealing of homologous regions in Second round PCR: Separate and purify fragment AB and CD by agarose gel electrophoresis and DNA gel extraction. Measure the concentration of the two fragments. Dilute them into 1:1 as template. Set up PCR system:</li> | + | <li>Annealing of homologous regions in Second round PCR: Separate and purify fragment AB and CD by agarose gel electrophoresis and DNA gel extraction. Measure the concentration of the two fragments. Dilute them into 1:1 as template. Set up PCR system: |
| + | <table style="font-size:80%;padding:5px;margin:5px"> |
| + | <tr> |
| + | <th>Reagent</th> <th>Volume</th> |
| + | </tr> |
| + | <tr> |
| + | <td>ddH<sub>2</sub>O</td> <td>To 50 μL</td> |
| + | </tr> |
| + | <tr> |
| + | <td>2 x Phanta Max Buffer</td> <td>25 μL</td> |
| + | </tr> |
| + | <tr> |
| + | <td>dNTP</td> <td>1 μL</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Phanta</td> <td>1 μL</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Template</td> <td>0.08 pmol + 0.08 pmol</td> |
| + | </tr> |
| + | </table> |
| + | Set up reaction program: |
| + | <table style="font-size:80%;padding:5px;margin:5px"> |
| + | <tr> |
| + | <th>Procedure</th> <th>Temperature</th><th>Time</th><th>Cycle</th> |
| + | </tr> |
| + | <tr> |
| + | <td>Initialization</td> <td>94℃</td><td>5min</td><td>1</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Denaturation</td> <td>94℃</td><td>30s</td><td rowspan=3>12</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Annealing</td> <td>60/64/68/72℃</td><td>30s</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Extension</td> <td>72℃</td><td>1min/kb</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Final elongation</td> <td>72℃</td><td>7min</td><td>1</td> |
| + | </tr> |
| + | </table></li> |
| <li>Store the vials: Store prepared vials in refrigerator at -80℃.</li> | | <li>Store the vials: Store prepared vials in refrigerator at -80℃.</li> |
| </ol> | | </ol> |
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| <h2>Vector PCR</h2> | | <h2>Vector PCR</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Cryopreservation is a technique that store cells at a very low temperatures (-80℃) to reduce cell metabolic damage and enable long-term storage.</p> | + | <p>Vector PCR is used for generating a linear product.</p> |
| <ol> | | <ol> |
− | <li>Add cryoprotectant: Add 80% glycerin 500μL and bacterial fluid 1 000μL into Cryopreservation vials. Mix upside down gently.</li> | + | <li>Set up PCR system (25 μL): |
− | <li>Seal the vials: Stick sellotape around the label.</li>
| + | <table style="font-size:80%;padding:5px;margin:5px"> |
− | <li>Store the vials: Store prepared vials in refrigerator at -80℃.</li> | + | <tr> |
− | </ol>
| + | <th>Reagent</th> <th>Volume</th> |
| + | </tr> |
| + | <tr> |
| + | <td>ddH<sub>2</sub>O</td> <td>To 25 μL</td> |
| + | </tr> |
| + | <tr> |
| + | <td>2 x Phanta Max Buffer</td> <td>12.5 μL</td> |
| + | </tr> |
| + | <tr> |
| + | <td>dNTP</td> <td>0.5 μL</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Phanta</td> <td>0.5 μL</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Template</td> <td>Plasmid: 0.5 μL</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Forward Primer</td> <td>1 μL</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Reverse Primer</td> <td>1 μL</td> |
| + | </tr> |
| + | </table></li> |
| + | <li>Place the PCR tubes in a PCR amplifier.</li> |
| + | <li>Set up reaction program: |
| + | <table style="font-size:80%;padding:5px;margin:5px"> |
| + | <tr> |
| + | <th>Procedure</th> <th>Temperature</th><th>Time</th><th>Cycle</th> |
| + | </tr> |
| + | <tr> |
| + | <td>Initialization</td> <td>95℃</td><td>30s</td><td>1</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Denaturation</td> <td>95℃</td><td>15s</td><td rowspan=3>40</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Annealing</td> <td>72℃</td><td>15s</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Extension</td> <td>72℃</td><td>30s/kb</td> |
| + | </tr> |
| + | <tr> |
| + | <td>Final elongation</td> <td>72℃</td><td>5min</td><td>1</td> |
| + | </tr> |
| + | </table></li> |
| + | <li>Incubate: Incubate at 16℃ until the PCR product is picked up. </li> |
| + | </ol> |
| </div> | | </div> |
| <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> | | <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> |
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| <h2>Agarose Gel Electrophoresis</h2> | | <h2>Agarose Gel Electrophoresis</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Agarose gel electrophoresis is performed to separate and confirm whether our plasmids were constructed properly.</p> | + | <p>Agarose gel electrophoresis is performed to separate and confirm whether our plasmids were constructed properly.</p> |
| <ol> | | <ol> |
− | <li>Make gel solution: Add 0.7g agarose, 70ml TAE buffer into a glass bottle and heat in a micro-oven for 2 min. Cool the liquid agarose gel to lower than 60℃ and decant the liquid agarose gel into an agarose gel tank. Add 8 μl EB into the liquid agarose gel and place the electrophoresis comb.</li> | + | <li>Make gel solution: Add 0.7g agarose, 70ml TAE buffer into a glass bottle and heat in a micro-oven for 2 min. Cool the liquid agarose gel to lower than 60℃ and decant the liquid agarose gel into an agarose gel tank. Add 8 μL EB into the liquid agarose gel and place the electrophoresis comb.</li> |
| <li>Load the gel: Place the solid agarose gel in an electrophoresis device. Add 10xDNA Loading Buffer in the DNA sample, mix them up gently and carefully pipette the sample into the sample loading chambers.</li> | | <li>Load the gel: Place the solid agarose gel in an electrophoresis device. Add 10xDNA Loading Buffer in the DNA sample, mix them up gently and carefully pipette the sample into the sample loading chambers.</li> |
| <li>Electrophoresis: Cover the lid of the electrophoresis device, set the electrophoresis time and start electrophoresis.</li> | | <li>Electrophoresis: Cover the lid of the electrophoresis device, set the electrophoresis time and start electrophoresis.</li> |
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| <h2>DNA Gel Extraction</h2> | | <h2>DNA Gel Extraction</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>DNA Gel Extraction is to extract desired DNA from an agarose gel after agarose gel electrophoresis.</p> | + | <p>DNA Gel Extraction is to extract desired DNA from an agarose gel after agarose gel electrophoresis.</p> |
| <ol> | | <ol> |
| <li>Cut the DNA gel: place the gel under UV light and find the DNA band of the desired nucleotide length. b) Cut the gel containing desired DNA and put it into an Eppendorf tube.</li> | | <li>Cut the DNA gel: place the gel under UV light and find the DNA band of the desired nucleotide length. b) Cut the gel containing desired DNA and put it into an Eppendorf tube.</li> |
− | <li>Melt the DNA gel: Use Vazyme® DNA Gel Extraction Kit. Add 300 μl buffer GDP to the Eppendorf tube and incubate at 55℃. Spin briefly.</li> | + | <li>Melt the DNA gel: Use Vazyme<sup>®</sup> DNA Gel Extraction Kit. Add 300 μL buffer GDP to the Eppendorf tube and incubate at 55℃. Spin briefly.</li> |
− | <li>Pure the DNA gel: Insert a Fast Mini Columns-G into a 2 ml Collection Tube, transfer the solution maximally of 700 μl once a time to a filtration column, centrifuge at 12,000 x g for 30 ~ 60 sec. Discard the filtrate and reuse the Collection Tube, add 600 μl of Buffer GW (with ethanol added) to the filtration column, centrifuge at 12,000 x g for 60 sec. Pure the left solution in the same way.</li> | + | <li>Pure the DNA gel: Insert a Fast Mini Columns-G into a 2 ml Collection Tube, transfer the solution maximally of 700 μL once a time to a filtration column, centrifuge at 12,000 x g for 30 - 60s. Discard the filtrate and reuse the Collection Tube, add 600 μL of Buffer GW (with ethanol added) to the filtration column, centrifuge at 12,000 x g for 60s. Pure the left solution in the same way.</li> |
− | <li>Filtrate DNA: Discard the filtrate and reuse the Collection Tube, centrifuge the empty column at 12,000 x g for 2 min. Insert the column into a clean 1.5 ml Eppendorf tube and incubate at 55℃ for 5 min. Add 7 μl ~ 30 μl of ddH2O (incubated at 55℃ in advance) to the center of the column membrane, incubate at room temperature for 2 min, and then centrifuge at 12,000 x g for 1min. Discard the filtration column. Measure the DNA concentration by Nanodrop 2000.</li> | + | <li>Filtrate DNA: Discard the filtrate and reuse the Collection Tube, centrifuge the empty column at 12,000 x g for 2 min. Insert the column into a clean 1.5 mL Eppendorf tube and incubate at 55℃ for 5 min. Add 7 μL - 30 μL of ddH<sub>2</sub>O (incubated at 55℃ in advance) to the center of the column membrane, incubate at room temperature for 2 min, and then centrifuge at 12,000 x g for 1min. Discard the filtration column. Measure the DNA concentration by Nanodrop 2000.</li> |
| <li>Store DNA at -20℃.</li> | | <li>Store DNA at -20℃.</li> |
| </ol> | | </ol> |
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| <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> | | <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> |
| | | |
− | <h2>Restriction Enzyme Double Digestion</h2> | + | <h2>Restriction Enzyme Double Digestion</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Double digestion reaction is performed to create mismatch ends for directional insertion.</p> | + | <p>Double digestion reaction is performed to create mismatch ends for directional insertion.</p> |
| <ol> | | <ol> |
− | <li>Add DNA fragment and vector at a mole ratio of 2:1~4:1 (total 1μg), 5 μl NEB CutSmart | + | <li>Add DNA fragment and vector at a mole ratio of 2:1 - 4:1 (total 1μg), 5 μL NEB CutSmart |
− | buffer, 1 μl of both restriction enzymes and ddH2O up to 50 μl to set up the reaction. | + | buffer, 1 μL of both restriction enzymes and ddH<sub>2</sub>O up to 50 μL to set up the reaction. |
| </li> | | </li> |
| <li>Incubate at 37℃ overnight.</li> | | <li>Incubate at 37℃ overnight.</li> |
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| <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> | | <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> |
| | | |
− | <h2>ClonExpress ligation reaction</h2> | + | <h2>ClonExpress ligation reaction</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>ClonExpress ligation reaction is performed to insert our DNA fragments into vector.</p> | + | <p>ClonExpress ligation reaction is performed to insert our DNA fragments into vector.</p> |
| <ol> | | <ol> |
− | <li>Set up ClonExpress ligation system: | + | <li>Set up ClonExpress ligation system: |
− | <table> | + | <table style="font-size:80%;padding:5px;margin:5px"> |
| <tr> | | <tr> |
| <th>Reagent</th> <th>Volume</th> | | <th>Reagent</th> <th>Volume</th> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>ddH2O</td> <td>To 5 µl</td> | + | <td>ddH<sub>2</sub>O</td> <td>To 5 μL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
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| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>2 x ClonExpress Mix</td> <td>2.5 µl</td> | + | <td>2 x ClonExpress Mix</td> <td>2.5 μL</td> |
| </tr> | | </tr> |
| </table></li> | | </table></li> |
| + | <li>Incubate at 50℃ for 30 minutes. Transform the DNA into bacteria.</li> |
| </ol> | | </ol> |
| </div> | | </div> |
| <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> | | <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> |
− | <h2>Plasmid transformation</h2> | + | <h2>Plasmid transformation</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Plasmid transformation is performed to transfer plasmids into the host bacteria. We transform our plasmids into DH5α E.coli to amplify them and BL21 to testify function of our plasmids.</p> | + | <p>Plasmid transformation is performed to transfer plasmids into the host bacteria. We transform our plasmids into DH5α <i>E. coli</i> to amplify them and BL21 to testify function of our plasmids.</p> |
| <ol> | | <ol> |
− |
| + | |
− | <li>Thaw all reagents on ice. And add 20 μl competent E.coli cells into the ligation product.</li> | + | <li>Thaw all reagents on ice. And add 20 μL competent <i>E. coli</i> cells into the ligation product.</li> |
− | <li>Heat shock at 42℃ for 45 sec and then cool the mixture on ice for 2 min. </li> | + | <li>Heat shock at 42℃ for 45s and then cool the mixture on ice for 2min. </li> |
− | <li>Add 900 μl liquid SOC or LB medium (without antibiotic) into the mixture and shaking culture at 37℃ for 1h.</li> | + | <li>Add 900 μL liquid SOC or LB medium (without antibiotic) into the mixture and shaking culture at 37℃ for 1h.</li> |
| <li>Evenly spread the liquid culture on a solid culture medium and incubate at 37℃ overnight for colonies forming on the plate.</li> | | <li>Evenly spread the liquid culture on a solid culture medium and incubate at 37℃ overnight for colonies forming on the plate.</li> |
| </ol> | | </ol> |
| </div> | | </div> |
| <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> | | <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> |
− | <h2>Plasmid Miniprep (Vazyme® FastPure Plasmid Mini Kit)</h2> | + | <h2>Plasmid Miniprep (Vazyme<sup>®</sup> FastPure Plasmid Mini Kit)</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Plasmid Miniprep is performed to is extract plasmid DNA from bacteria.</p> | + | <p>Plasmid Miniprep is performed to is extract plasmid DNA from bacteria.</p> |
− | <ol><li>Harvest 1~ 5 ml overnight cultured (12 ~ 16 hours) bacterial cells into a centrifuge | + | <ol><li>Harvest 1 - 5 mL overnight cultured (12 - 16h) bacterial cells into a centrifuge |
− | tube, centrifuge at 10,000 x g for 1 min, discard the supernatant and invert the tube | + | tube, centrifuge at 10,000 x g for 1min, discard the supernatant and invert the tube |
| on the absorbent paper to dry. | | on the absorbent paper to dry. |
| </li> | | </li> |
− | <li>Add 250 μl of Buffer P1 (add RNase A before use), mix thoroughly by vortex or pipetting up and down.</li> | + | <li>Add 250 μL of Buffer P1 (add RNase A before use), mix thoroughly by vortex or pipetting up and down.</li> |
− | <li>Add 250 μl of Buffer P2, mix thoroughly by softly inverting the tube 8 ~ 10 times | + | <li>Add 250 μL of Buffer P2, mix thoroughly by softly inverting the tube 8 - 10 times |
| to assure complete lysis. | | to assure complete lysis. |
| </li> | | </li> |
− | <li>Add 350 μl of Buffer P3, mix gently and thoroughly by inverting the tube 8 ~ 10 times to neutralize Buffer P2 until a flocculent white precipitate forms and centrifuge at 13,000 x g for 10 min.</li> | + | <li>Add 350 μL of Buffer P3, mix gently and thoroughly by inverting the tube 8 - 10 times to neutralize Buffer P2 until a flocculent white precipitate forms and centrifuge at 13,000 x g for 10min.</li> |
− | <li>Insert a FastPure DNA Mini Column into a 2 ml Collection Tube, transfer the supernatant from step 4 to the Filtration Column, centrifuge at 13,000 x g for 30 ~ 60 sec, discard the filtrate and reuse the Collection Tube.</li> | + | <li>Insert a FastPure DNA Mini Column into a 2 mL Collection Tube, transfer the supernatant from step 4 to the Filtration Column, centrifuge at 13,000 x g for 30 - 60s, discard the filtrate and reuse the Collection Tube.</li> |
− | <li>Add 600 μl of Buffer PW2 (with ethanol added in) to the Filtration Column, centrifuge at 13,000 x g for 30 ~ 60 sec, discard the filtrate and reuse the Collection Tube. Centrifuge the empty Filtration Column for l min at 13,000 x g.</li> | + | <li>Add 600 μL of Buffer PW2 (with ethanol added in) to the Filtration Column, centrifuge at 13,000 x g for 30 - 60s, discard the filtrate and reuse the Collection Tube. Centrifuge the empty Filtration Column for l min at 13,000 x g.</li> |
− | <li>Insert the Column into a clean 1.5 ml microcentrifuge tube, add 30 ~ 100 μl of Elution Buffer to the center of the Column membrane, incubate at room temperature for 2 min, centrifuge at 13,000 x g for 1min. Discard the Filtration Columns, store DNA at -20℃. </li></ol> | + | <li>Insert the Column into a clean 1.5 mL microcentrifuge tube, add 30 - 100 μL of Elution Buffer to the center of the Column membrane, incubate at room temperature for 2min, centrifuge at 13,000 x g for 1min. Discard the Filtration Columns, store DNA at -20℃. </li> |
| + | </ol> |
| </div> | | </div> |
| <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> | | <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> |
| <h2>SDS-PAGE</h2> | | <h2>SDS-PAGE</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>SDS-PAGE is performed for the separation of polypeptides and confirm whether our circuits expressed properly.</p> | + | <p>SDS-PAGE is performed for the separation of polypeptides and confirm whether our circuits expressed properly.</p> |
| <ol> | | <ol> |
− | <li>Prepare 10ml 10% Running Gel solution: Add4.1 ml ddH2O, 3.3 ml 30% Acrylamide/Bis (29:1 or 37.5:1), 2.5 ml 1.5M Tris-HCl pH8.8, 100 μl 10% SDS, 50 μl 10% APS, 5 μl TEMED. Mix them thoroughly.</li> | + | <li>Prepare 10ml 10% Running Gel solution: Add4.1 mL ddH<sub>2</sub>O, 3.3 mL 30% Acrylamide/Bis (29:1 or 37.5:1), 2.5 mL 1.5 M Tris-HCl pH8.8, 100 μL 10% SDS, 50 μL 10% APS, 5 μL TEMED. Mix them thoroughly.</li> |
− | <li>Prepare 2ml 4% Stacking Gel solution: Add 1.22 ml ddH2O, 0.26ml 30% Acrylamide/Bis (29:1 or 37.5:1), 0.5ml 0.5M Tris-HCl pH6.8, 20 μl 10% SDS, 20 μl 10% APS, 2 μl TEMED. Mix them thoroughly. </li> | + | <li>Prepare 2ml 4% Stacking Gel solution: Add 1.22 ml ddH<sub>2</sub>O, 0.26ml 30% Acrylamide/Bis (29:1 or 37.5:1), 0.5 mL 0.5 M Tris-HCl pH6.8, 20 μL 10% SDS, 20 μL 10% APS, 2 μL TEMED. Mix them thoroughly. </li> |
− | <li>Prepare the protein sample: Add 1 ml bacterial cells per time into a centrifuge tube, centrifuge at 12,000 x g for 1 min, discard the supernatant. Dilute SDS sample buffer to 1x. Add 1 x SDS Loading to 3000 cells per 1ul, mix thoroughly by vortex or pipetting up and down until there is no visible precipitation. Incubate at 99℃ for 5 min.</li> | + | <li>Prepare the protein sample: Add 1 ml bacterial cells per time into a centrifuge tube, centrifuge at 12,000 x g for 1min, discard the supernatant. Dilute SDS sample buffer to 1x. Add 1 x SDS Loading to 3000 cells per 1 μL, mix thoroughly by vortex or pipetting up and down until there is no visible precipitation. Incubate at 99℃ for 5min.</li> |
− | <li>Make the gel: Assemble the gel cassette and make sure it not to leak. Fill the gel cassette with the Running Gel softly and fill up the cassette with ddH2O. Keep it still for 10~20 min until the water layer can be observed. Pour out the ddH2O completely and fill up the cassette with Stacking Gel. Insert the comb and take care not to catch bubbles under the teeth. Keep it still.</li> | + | <li>Make the gel: Assemble the gel cassette and make sure it not to leak. Fill the gel cassette with the Running Gel softly and fill up the cassette with ddH<sub>2</sub>O. Keep it still for 10 - 20min until the water layer can be observed. Pour out the ddH<sub>2</sub>O completely and fill up the cassette with Stacking Gel. Insert the comb and take care not to catch bubbles under the teeth. Keep it still.</li> |
− | <li>Load the gel: Take off the cassette and assemble the gel running stand. Fill the stand with 1 x SDS running buffer and remove the combs from the gel. Mix up Marker with 1 x SDS Loading. Load 15 μl marker mixture into the wells.</li> | + | <li>Load the gel: Take off the cassette and assemble the gel running stand. Fill the stand with 1 x SDS running buffer and remove the combs from the gel. Mix up Marker with 1 x SDS Loading. Load 15 μL marker mixture into the wells.</li> |
| <li>Electrophoresis: Cover the lid of the electrophoresis device, and start electrophoresis at 200 V until the dye front is nearly at the bottom of the gel. </li> | | <li>Electrophoresis: Cover the lid of the electrophoresis device, and start electrophoresis at 200 V until the dye front is nearly at the bottom of the gel. </li> |
− | <li>Stain the gel: Submerge the whole piece of the disassembled gel with 0.1% Coomassie Blue dye for 30 min.</li> | + | <li>Stain the gel: Submerge the whole piece of the disassembled gel with 0.1% Coomassie Blue dye for 30min.</li> |
− | <li>Destain the gel: Pour out the 0.1% Coomassie Blue dye and wash it using ddH2O. Destain with destaining solution for 30min. Change the destaining solution to destain until it clear.</li> | + | <li>Destain the gel: Pour out the 0.1% Coomassie Blue dye and wash it using ddH<sub>2</sub>O. Destain with destaining solution for 30min. Change the destaining solution to destain until it clear.</li> |
− | <li>Scan the gel.</li> | + | <li>Scan the gel.</li> |
| </ol> | | </ol> |
| </div> | | </div> |
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| <h2>SDS-PAGE Gradient Gel</h2> | | <h2>SDS-PAGE Gradient Gel</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>SDS-PAGE is performed for the separation of caap and confirm whether our circuits functioned properly.</p> | + | <p>SDS-PAGE is performed for the separation of caap and confirm whether our circuits functioned properly.</p> |
| <ol> | | <ol> |
| <li>Start the device: Put the container on the electromagnetic heating device. Increase the speed of the rotor gradually to 260 RPM.</li> | | <li>Start the device: Put the container on the electromagnetic heating device. Increase the speed of the rotor gradually to 260 RPM.</li> |
− | <li>Prepare Gel solution: 4% and 20% Gel solution, can be prepared directly according to SDS-PAGE protocol. And 1.5 times of APS concentration can be added in autumn.</li> | + | <li>Prepare Gel solution: 4% and 20% Gel solution, can be prepared directly according to SDS-PAGE protocol. And 1.5 times of APS concentration should be added.</li> |
| <li>Gradient formation: Add 4% glue slowly into the valve, and then add 20% glue. Mix them by the rotor. Wait about 2 hours for the glue to concrete.</li> | | <li>Gradient formation: Add 4% glue slowly into the valve, and then add 20% glue. Mix them by the rotor. Wait about 2 hours for the glue to concrete.</li> |
| <li>Store the gel: Remove the solidified glue one by one. Soak them in 1×SDS, and put them into a refrigerator at 4℃ under the counter for preservation.</li> | | <li>Store the gel: Remove the solidified glue one by one. Soak them in 1×SDS, and put them into a refrigerator at 4℃ under the counter for preservation.</li> |
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| <h2>IPTG induction experiment </h2> | | <h2>IPTG induction experiment </h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>xxxxxxxxxxx</p>
| + | |
| <ol> | | <ol> |
− | <li>Reconnection: Take 10 ml and 5 ml LB liquid medium in two test tubes, 10ml one is used as control group and 5ml one is for experiment group. Add 500× ampicillin 20 μl and 10μl, respectively. Culture 6h. Add 1 ml bacteria solution to experiment group and divided evenly into two tubes (3mL each) for ipTG-induced and non-induced groups. Another 1ml bacteria was used to measure initial OD.</li> | + | <li>Reconnection: Take 10 mL and 5 mL LB liquid medium in two test tubes, 10 mL one is used as control group and 5 mL one is for experiment group. Add 500× ampicillin 20 μL and 10 μL, respectively. Culture 6h. Add 1 mL bacteria solution to experiment group and divided evenly into two tubes (3 mL each) for ipTG-induced and non-induced groups. Another 1 mL bacteria was used to measure initial OD.</li> |
| <li>Measure OD: Measured OD value once per 30min and once per 15min after OD reached 0.2.</li> | | <li>Measure OD: Measured OD value once per 30min and once per 15min after OD reached 0.2.</li> |
− | <li>Induce: When OD value reached about 0.6, add 500mM IPTG reach final concentration of 1mM. Incubate for 3 hours.</li> | + | <li>Induce: When OD value reached about 0.6, add 500mM IPTG reach final concentration of 1 mM. Incubate for 3 hours.</li> |
| </ol> | | </ol> |
| </div> | | </div> |
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| <h2>Anhydrotetracycline induction experiment</h2> | | <h2>Anhydrotetracycline induction experiment</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Cryopreservation is a technique that store cells at a very low temperatures (-80℃) to reduce cell metabolic damage and enable long-term storage.</p>
| + | |
| <ol> | | <ol> |
− | <li>Add cryoprotectant: Add 80% glycerin 500μL and bacterial fluid 1 000μL into Cryopreservation vials. Mix upside down gently.</li> | + | <li>Dilute aTc: Dilute 2 mg/ mL aTc solution into 100 ng/ mL, 200 ng/ mL and 400 ng/ mL.</li> |
− | <li>Seal the vials: Stick sellotape around the label.</li>
| + | <li>Induce: Add 3 mL LB medium (with kan), 200 μL ON culture and 32 μL corresponding inducer (in one of the test tubes add 32 μL LB medium as control) into 3 mL bacteria solution. </li> |
− | <li>Store the vials: Store prepared vials in refrigerator at -80℃.</li>
| + | <li>Measure: Add 300 μL of each test tube to the microplate reader in triplet, and measure the t0 at the correct wavelength and OD600. Put the test tubes in the shaker at 37℃ and 250 rpm. After 4 hours measure the t4, after 8 hours measure the t8 and after 12h measure the t<sub>12</sub>. </li> |
| </ol> | | </ol> |
| </div> | | </div> |
| <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> | | <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> |
| | | |
− | <h2>Growth Curve Measurement</h2> | + | <h2 id="kill_switch_plan">Growth Curve Measurement</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Growth Curve Measurement is used to characterize our Kill Switches.</p> | + | <p>Growth Curve Measurement is used to characterize our Kill Switches.</p> |
| <ol> | | <ol> |
− | <li>Plasmids construction and transformation: Insert DNA fragments of BBa_K3036004, BBa_K3606027 and BBa_K3606028 in to pSB1C3. Transform the two kinds of constructed plasmids into DH5α strain as experimental groups and empty pSB1C plasmids as control group. Culture three groups in 60mL LB medium (with 50 ng/µl ampicillin) at 37℃ overnight.</li> | + | <li>Plasmids construction and transformation: Insert DNA fragments of BBa_K3036004, BBa_K3606027 and BBa_K3606028 into pSB1C3. Transform the two kinds of constructed plasmids into DH5α strain as experimental groups and empty pSB1C plasmids as control group. Culture three groups in 60mL LB medium (with 50 ng/ μL ampicillin) at 37℃ overnight.</li> |
| <li>Cold treatment: Divide each group into two test tubes for 30℃-culture groups and 37℃-culture groups. (3 for each temperature). </li> | | <li>Cold treatment: Divide each group into two test tubes for 30℃-culture groups and 37℃-culture groups. (3 for each temperature). </li> |
− | <li>Measure growth situation: Extract 5μl bacteria solution from each test tube every 1h. Diluted each bacteria solution to 10^7 times and culture them on three LB plate (with 50 ng/µl ampicillin) at 37℃ for 24h. Count the number of colonies in 5 cm^2 per plate after cultured for 24h at 37℃. </li> | + | <li>Measure growth situation: Extract 5 μL bacteria solution from each test tube every 1h. Diluted each bacteria solution to 10^7 times and culture them on three LB plate (with 50 ng/ μL ampicillin) at 37℃ for 24h. Count the number of colonies in 5 cm^2 per plate after cultured for 24h at 37℃. </li> |
− | <li>Draw the growth curve.</li>
| + | <li>Draw the growth curve.</li> |
| </ol> | | </ol> |
| </div> | | </div> |
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| <h2>Methylthymol Blue Method for Blood Calcium Measurement</h2> | | <h2>Methylthymol Blue Method for Blood Calcium Measurement</h2> |
| <div class="column full_size"> | | <div class="column full_size"> |
− | <p>Methylthymol Blue Method is used to determine the concentration of calcium chromogenic reaction.</p> | + | <p>Methylthymol Blue Method is used to determine the concentration of calcium chromogenic reaction.</p> |
| <ol> | | <ol> |
− | <li>Prepare solution 1: | + | <li>Prepare solution 1 |
− | <table> | + | <table style="font-size:80%;padding:5px;margin:5px"> |
| <tr> | | <tr> |
| <th>Reagent</th> <th>Volume</th> | | <th>Reagent</th> <th>Volume</th> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>H2O</td> <td>To 45ml</td> | + | <td>H<sub>2</sub>O</td> <td>To 45 mL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>MTB</td> <td>0.009g</td> | + | <td>MTB</td> <td>0.009 g</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>8-Hydroxyquinoline</td> <td>6.096g</td> | + | <td>8-Hydroxyquinoline</td> <td>6.096 g</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>HCl</td> <td>0.55785ml</td> | + | <td>HCl</td> <td>0.55785 mL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Urea</td> <td>2.5 µl</td> | + | <td>Urea</td> <td>8.109g</td> |
| </tr> | | </tr> |
| </table></li> | | </table></li> |
− | <li>Prepare solution 2:</li> | + | <li>Prepare solution 2</li> |
− | <table> | + | <table style="font-size:80%;padding:5px;margin:5px"> |
| <tr> | | <tr> |
| <th>Reagent</th> <th>Volume</th> | | <th>Reagent</th> <th>Volume</th> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>H2O</td> <td>To 45ml</td> | + | <td>H2O</td> <td>To 45 mL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Ethanolamine</td> <td>9ml</td> | + | <td>Ethanolamine</td> <td>9 mL</td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td>Urea</td> <td>2.5 µl</td> | + | <td>Urea</td> <td>8.109g</td> |
| </tr> | | </tr> |
− | </table></li> | + | </table> |
− | <li>Set up chromogenic reaction: Take 1ml solution 1 and 1ml solution 2 to make the application solution. Add 34ul standard calcium ion sample into the system in proportion of 60:1and mix it.</li> | + | <li>Set up chromogenic reaction: Take 1ml solution 1 and 1ml solution 2 to make the application solution. Add 34 μL standard calcium ion sample into the system in proportion of 60:1 and mix it.</li> |
− | <li>Cassist anti-interference capability test: Add 34ul standard calcium ion sample with an interfering substance (including 15mM magnesium ions, 100mM sucrose, 80 g/L serum protein, 40 g/L PEG8000) at a fixed concentration into the system and mix it.</li>
| + | <li>Measure the absorbance: Wait for about 3 to 5 min and measure the absorbance of the solution with a spectrophotometer.</li> |
− | <li>Measure the absorbance: Wait for about 3 to 5 minutes and measure the absorbance of the solution with a spectrophotometer.</li> | + | <li>Change the standard calcium ion concentration from 0 to 20 mM and make multiple measurements to obtain the linearity curve.</li> |
− | <li>Change the standard calcium ion concentration from 0 to 20mmol and make multiple measurements to obtain the linearity curve.</li> | + | |
− | <li>Cassist anti-interference stability test: Measure the absorbance of the solution 1h, 2h, 3h, 6h, 12h, 24h, 2days, 7days.</li>
| + | |
| </ol> | | </ol> |
| </div> | | </div> |
| <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> | | <div class="clear"></div><!-- 一个章节结束需要clear来留白 --> |
− | | + | |
− |
| + | <div class="column full_size"> |
| + | <p>Click <a target="_blank" href="https://static.igem.org/mediawiki/2020/0/0a/T--Fudan--Protocol.pdf">here</a> to download the protocols used by 2020 Fudan team, as a single PDF file.</p> |
| + | </div> |
| + | |
| + | <div class="clear"></div> |
| | | |
| <div class="column full_size"><div id="FudanSignature"> | | <div class="column full_size"><div id="FudanSignature"> |
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| <div class="container"><div class="row"> | | <div class="container"><div class="row"> |
| <div class="col m3 s12 row" | | <div class="col m3 s12 row" |
− | style="margin-top:4rem" > | + | style="margin-top:4rem" tabIndex="0" > |
| <a href="http://www.yfc.cn/" target="_blank"><img class="col s3 m6 l4 FudanSponsors" alt="Yunfeng Capital" src="https://static.igem.org/mediawiki/2020/b/ba/T--Fudan--YFcapital.svg"> </a> | | <a href="http://www.yfc.cn/" target="_blank"><img class="col s3 m6 l4 FudanSponsors" alt="Yunfeng Capital" src="https://static.igem.org/mediawiki/2020/b/ba/T--Fudan--YFcapital.svg"> </a> |
| <a href="http://www.fudan.edu.cn/en/" target="_blank"><img alt="Fudan University" class="col s3 m6 l4 FudanSponsors" src="https://static.igem.org/mediawiki/2020/9/9d/T--Fudan--sponsor2.svg"> </a> | | <a href="http://www.fudan.edu.cn/en/" target="_blank"><img alt="Fudan University" class="col s3 m6 l4 FudanSponsors" src="https://static.igem.org/mediawiki/2020/9/9d/T--Fudan--sponsor2.svg"> </a> |
| <a href="http://life.fudan.edu.cn/" target="_blank"><img class="col s3 m6 l4 FudanSponsors" alt="School of Life Sciences, Fudan University" src="https://static.igem.org/mediawiki/2018/1/1d/T--Fudan--schoolOfLifeSciencesIcon.png"> </a> | | <a href="http://life.fudan.edu.cn/" target="_blank"><img class="col s3 m6 l4 FudanSponsors" alt="School of Life Sciences, Fudan University" src="https://static.igem.org/mediawiki/2018/1/1d/T--Fudan--schoolOfLifeSciencesIcon.png"> </a> |
| <h3 class="col s12" | | <h3 class="col s12" |
− | style="text-align:left;font-size:1rem;margin:0;padding-left:0.68rem">Bone appetite: <i>make calcium supplement sustainable</i></h3> | + | style="text-align:left;font-size:1rem;margin:0;padding-left:0.68rem">Bone appetite: <i>make calcium supplement sustainable</i></h3 > |
| </div> | | </div> |
| <div id="footerNavList" class="col m9 s12 row"> | | <div id="footerNavList" class="col m9 s12 row"> |
| <div class="col s12 l6 row"> | | <div class="col s12 l6 row"> |
| <div class="col s12 m4"> | | <div class="col s12 m4"> |
− | <span><a href="/Team:Fudan/Description#Project">Project</a></span> | + | <span tabIndex="2"><a href="/Team:Fudan/Description#Project">Project</a></span> |
| <ul><li><a href="/Team:Fudan/Description">Description</a></li> | | <ul><li><a href="/Team:Fudan/Description">Description</a></li> |
| <li><a href="/Team:Fudan/Sustainable">Sustainable</a></li> | | <li><a href="/Team:Fudan/Sustainable">Sustainable</a></li> |
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| </ul></div> | | </ul></div> |
| <div class="col s12 m4"> | | <div class="col s12 m4"> |
− | <span><a href="/Team:Fudan/Notebook">Notebook</a></span> | + | <span tabIndex="3"><a href="/Team:Fudan/Notebook">Notebook</a></span> |
| <ul><li><a href="/Team:Fudan/Safety">Safety</a></li> | | <ul><li><a href="/Team:Fudan/Safety">Safety</a></li> |
| <li><a href="/Team:Fudan/Poster">Poster</a></li> | | <li><a href="/Team:Fudan/Poster">Poster</a></li> |
− | <li><a href="#">Video</a></li> | + | <li><a href="https://video.igem.org/videos/watch/7a0fee51-a637-4caf-aa97-a1d9bcafd3ba" target="_blank">Promotion</a></li> |
| + | <li><a href="#" target="_blank">Presentation</a></li> |
| + | <li><a href="/Team:Fudan/Entrepreneurship">Entrepreneurship</a></li> |
| </ul></div> | | </ul></div> |
| <div class="col s12 m4"> | | <div class="col s12 m4"> |
− | <span><a href="/Team:Fudan/Results">Results</a></span> | + | <span tabIndex="4"><a href="/Team:Fudan/Results">Results</a></span> |
| <ul><li><a href="/Team:Fudan/Contribution">Contribution</a></li><!-- replace Judging --> | | <ul><li><a href="/Team:Fudan/Contribution">Contribution</a></li><!-- replace Judging --> |
| + | <li><a href="/Team:Fudan/Implementation">Implementation</a></li> |
| <li><a href="/Team:Fudan/Engineering">Engineering</a></li> | | <li><a href="/Team:Fudan/Engineering">Engineering</a></li> |
| <li><a href="/Team:Fudan/Measurement">Measurement</a></li> | | <li><a href="/Team:Fudan/Measurement">Measurement</a></li> |
| <li><a href="/Team:Fudan/Model">Modeling</a></li> | | <li><a href="/Team:Fudan/Model">Modeling</a></li> |
− | <li><a href="/Team:Fudan/Entrepreneurship">Entrepreneurship</a></li>
| |
| </ul></div> | | </ul></div> |
| </div> | | </div> |
| <div class="col s12 l6 row"> | | <div class="col s12 l6 row"> |
| <div class="col s12 m4"> | | <div class="col s12 m4"> |
− | <span><a href="/Team:Fudan/Parts">Parts</a></span> | + | <span tabIndex="5"><a href="/Team:Fudan/Parts">Parts</a></span> |
| <ul><li><a href="/Team:Fudan/Parts#Basic">Basic part</a></li> | | <ul><li><a href="/Team:Fudan/Parts#Basic">Basic part</a></li> |
| <li><a href="/Team:Fudan/Parts#Composite">Composite part</a></li> | | <li><a href="/Team:Fudan/Parts#Composite">Composite part</a></li> |
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| </ul></div> | | </ul></div> |
| <div class="col s12 m4"> | | <div class="col s12 m4"> |
− | <span><a href="/Team:Fudan/Human_Practices">Outreach</a></span> | + | <span tabIndex="6"><a href="/Team:Fudan/Human_Practices">Outreach</a></span> |
| <ul><li><a href="/Team:Fudan/Human_Practices#Integrated">Integrated HP</a></li> | | <ul><li><a href="/Team:Fudan/Human_Practices#Integrated">Integrated HP</a></li> |
| <li><a href="/Team:Fudan/Education">Education</a></li> | | <li><a href="/Team:Fudan/Education">Education</a></li> |
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Line 801: |
| </ul></div> | | </ul></div> |
| <div class="col s12 m4"> | | <div class="col s12 m4"> |
− | <span><a href="/Team:Fudan/Team">Team</a></span> | + | <span tabIndex="7"><a href="/Team:Fudan/Team">Team</a></span> |
| <ul><li><a href="/Team:Fudan/Team">Members</a></li> | | <ul><li><a href="/Team:Fudan/Team">Members</a></li> |
| <li><a href="/Team:Fudan/Attributions">Attributions</a></li> | | <li><a href="/Team:Fudan/Attributions">Attributions</a></li> |
| <li><a href="/Team:Fudan/Partnership">Partnership</a></li> | | <li><a href="/Team:Fudan/Partnership">Partnership</a></li> |
| <li><a href="/Team:Fudan/Acknowledgement">Acknowledgement</a></li> | | <li><a href="/Team:Fudan/Acknowledgement">Acknowledgement</a></li> |
− | <li><a href="https://2019.igem.org/Team:Fudan-TSI/Heritage" target="_blank">Heritage</a></li> | + | <li><a href="/Team:Fudan/Heritage">Heritage</a></li> |
| </ul></div> | | </ul></div> |
| <div class="col s12 m4"> </div> | | <div class="col s12 m4"> </div> |