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− | #photo-left { background-image: url("/wiki/images/c/c1/T--NCKU_Tainan--sample2.jpg"); } | + | #photo-left { background-image: url("/wiki/images/9/9a/T--NCKU_Tainan--Notebook.png"); } |
| + | #line-left2, #line-right { display: none; } |
| + | .intro { margin: 20px 0; } |
| + | li { line-height:2.5em; font-size:20px;} |
| </style> | | </style> |
| <div class="container-fluid" style="margin-top:100px"> | | <div class="container-fluid" style="margin-top:100px"> |
− | <div class="head">NOTE / Construction</div> | + | <div class="head">NOTEBOOK / Overview</div> |
| <div class="content row"> | | <div class="content row"> |
| <div class="col-md-9"> | | <div class="col-md-9"> |
− | <div class="head2">Notebook - Construction</div> | + | <div class="head2">Notebook - Overview</div> |
− | <div class="title-line" id="sec1"></div> | + | <div class="intro">We divide our record - notebook into five parts:</div> |
− | <div class="title-content">Extracted plasmid from the bacteria provided by XMU<br>(pSB1C3-BBa_B0034, pSB1C3-BBa_B0015, pSB1C3-BBa_K592009)</div>
| + | <ol> |
− | <h5>2016.03.30</h5>
| + | <li><a href="/Team:NCKU_Tainan/Notebook_Construction">Construction</a></li> |
− | <p>We got the bacteria with Biobrick from XMU.</p>
| + | <li><a href="/Team:NCKU_Tainan/Notebook_Functional_Test">Functional Test</a></li> |
− | <h5>2016.04.01</h5>
| + | <li><a href="/Team:NCKU_Tainan/Notebook_Device_Design">Device Design</a></li> |
− | <p>Pre-culture: 3 ml of LB (with Chloramphenicol) was inoculated with one colony from LB agar plate.</p>
| + | <li><a href="/Team:NCKU_Tainan/Notebook_Protocols">Protocols</a></li> |
− | <h5>2016.04.02</h5>
| + | <li><a href="/Team:NCKU_Tainan/Notebook_Model">Model</a></li> |
− | <p>Culture: 10 ml of LB (with Chloramphenicol) culture with 100 ml/μL pre-cultured bacteria. </p>
| + | </ol> |
− | <p>And grow up at 37 degree for 10-12 hours.</p>
| + | |
− | <h5>2016.04.03</h5>
| + | |
− | <p>Extracted the plasmid, and measured the concentration.</p>
| + | |
− | <p>Store the plasmid at -20 degree.</p>
| + | |
− | | + | |
− | <div class="title-line" id="sec2"></div>
| + | |
− | <div class="title-content">Got the glucose sensitive promoter (PpI, Pcar) by PCR</div> | + | |
− | <h5>2016.04.16</h5>
| + | |
− | <p>PCR for PpI & Pcar.<br>
| + | |
− | <i class="glyphicon glyphicon-ok"></i>Result: After gel purified, the concentration of the DNA was too low to do construction.</p>
| + | |
− | <h5>2016.04.17</h5>
| + | |
− | <p>PCR for PpI & Pcar again (in big scale).</p>
| + | |
− | <p>Purified the PCR product and cloned to T-vector.</p>
| + | |
− | <h5>2016.04.18</h5>
| + | |
− | <p>Confirmed the white colony by PCR (using M13F & M13R as the primer)<br>
| + | |
− | <i class="glyphicon glyphicon-ok"></i>Result: Some of the colonies were correct.</p>
| + | |
− | <p>Pre-culture: 3 ml of LB (with Ampicillin) was inoculated with one correct colony from the agar plate.</p>
| + | |
− | <h5>2016.04.19</h5>
| + | |
− | <p>Extracted plasmid and confirmed plasmid size by gel electrophoresis.<br>
| + | |
− | <i class="glyphicon glyphicon-ok"></i>Result: The size of pMD19T-PpI and pMD19T-Pcar were correct.</p>
| + | |
− | <h5>2016.04.20</h5>
| + | |
− | <p>Culture: 10 ml of LB (with Ampicillin) cultured with 100 ml/μL pre-cultured bacteria.</p>
| + | |
− | <p>Grow up at 37 degree for 8 hours and stored the bacteria at -70 refrigerator.</p>
| + | |
− | | + | |
− | <div class="title-line" id="sec3"></div>
| + | |
− | <div class="title-content">Constructed pSB1C3-B0034-K592009</div>
| + | |
− | <h5>2016.04.30</h5>
| + | |
− | <p>Digested pSB1C3-B0034 (<i>SpeI,PstI</i>) and pSB1C3-K592009 (<i>XbaI,PstI</i>)</p>
| + | |
− | <p>Ligated K592009 (insert) to pSB1C3-B0034 (vector) and transformed the product.</p>
| + | |
− | <h5>2016.05.01</h5>
| + | |
− | <p>Confirmed by colony PCR (using Prefix-F & Suffix-R as the primer).</p>
| + | |
− | <p>Pre-culture: 3 ml of LB (with Chloramphenicol) was inoculated with one correct colony from the agar plate.</p>
| + | |
− | <h5>2016.05.02</h5>
| + | |
− | <p>Extracted plasmid and confirmed plasmid size by gel electrophoresis.<br>
| + | |
− | <i class="glyphicon glyphicon-ok"></i>Result: The size of pSB1C3-B0034-K592009 was correct.
| + | |
− | </p>
| + | |
− | <h5>2016.05.03</h5>
| + | |
− | <p>Culture: 10 ml of LB (with Chloramphenicol) cultured with 100ml/μL pre-cultured bacteria.</p>
| + | |
− | <p>Grow up at 37 degree for 8 hours and stored the bacteria at -70 refrigerator.</p>
| + | |
− | | + | |
− | <div class="title-line" id="sec3"></div>
| + | |
− | <div class="title-content">Construct pMD19T-Pcar-B0034-K592009 and pMD19T-PpI-B0034-K592009</div>
| + | |
− | <h5>2016.05.07</h5>
| + | |
− | <p>Digested pSB1C3-B0034-K592009 (<i>XbaI,PstI</i>), pMD19T-Pcar (<i>SpeI,PstI</i>) and pMD19T-PpI (<i>SpeI,PstI</i>)
| + | |
− | </p><p>Ligated B0034-K592009 (insert) to pMD19T-Pcar (vector) and pMD19T-Pcar (vector). </p>
| + | |
− | <p>Transformed the product.</p>
| + | |
− | <h5>2016.05.08</h5>
| + | |
− | <p>Confirmed by colony PCR (using M13F & M13R as the primer).</p>
| + | |
− | <p>Pre-culture: 3 ml of LB (with Ampicillin) was inoculated with one correct colony from the agar plate.</p>
| + | |
− | <h5>2016.05.09</h5>
| + | |
− | <p>Extracted plasmid and confirm plasmid size by gel electrophoresis.<br>
| + | |
− | <i class="glyphicon glyphicon-ok"></i>Result: The size of pMD19T-Pcar-B0034-K592009 and pMD19T-PpI-B0034-K592009 were correct.</p>
| + | |
− | <h5>2016.05.10</h5>
| + | |
− | <p>Culture: 10 ml of LB (with Ampicillin) cultured with 100 ml/μL pre-cultured bacteria.</p>
| + | |
− | <p>Grow up at 37 degree for 8 hours and stored the bacteria at -70 refrigerator.</p>
| + | |
− | | + | |
− | <div class="title-line" id="sec3"></div>
| + | |
− | <div class="title-content">We transformed BioBricks from the 2016 igem distribution<br>
| + | |
− | (BBa_J23110, BBa_J23101,BBa_B0031,BBa_B0032,BBa_E1010)</div>
| + | |
− | <h5>2016.06.03</h5>
| + | |
− | <p>Transformed 3 ml/μL biobrick to 100 ml/μL DH5α competent cell by heat shock.<br>
| + | |
− | <i class="glyphicon glyphicon-ok"></i>Result: The transformation of BBa_J23110, BBa_B0032 and BBa_E1010 was successful.<br>
| + | |
− | <i class="glyphicon glyphicon-remove"></i>Result: The transformation of BBa_J23110, BBa_B0032 and BBa_E1010 was fail.</p>
| + | |
− | <h5>2016.06.04</h5>
| + | |
− | <p>Pre-culture: 4 ml of LB (with Chloramphenicol) was inoculated with one colony from LB agar plate.</p>
| + | |
− | <p>Extracted plasmid by Plasmid miniPREP Kit and confirmed plasmid size by gel electrophoresis.</p>
| + | |
− | <h5>2016.06.05</h5>
| + | |
− | <p>Culture: 10 ml of LB (with Chloramphenicol) was inoculated with one colony from LB agar plate. And grow up at 37 degree for 10-12 hours.</p>
| + | |
− | <h5>2016.06.06</h5>
| + | |
− | <p>Extracted the plasmid, and measure the concentration.</p>
| + | |
− | <p>Stored the plasmid at -20 degree.</p>
| + | |
− | <h5>2016.06.07</h5>
| + | |
− | <p>Transformed 5 ml/μL biobrick to 100 ml/μL DH5α competent cell by heat shock.<br>
| + | |
− | (BBa_J23110, BBa_B0032 and BBa_E1010)<br>
| + | |
− | <i class="glyphicon glyphicon-ok"></i>Result: The transformation of BBa_J23110, BBa_B0032 and BBa_E1010 were successful.</p>
| + | |
− | <h5>2016.06.08</h5>
| + | |
− | <p>Pre-culture: 4 ml of LB (with Chloramphenicol) was inoculated with one colony from LB agar plate.</p>
| + | |
− | <p>Extracted plasmid by Plasmid miniPREP Kit and confirmed plasmid size by gel electrophoresis.</p>
| + | |
− | <h5>2016.06.09</h5>
| + | |
− | <p>Culture: 10 ml of LB (with Chloramphenicol) was inoculated with one colony from LB agar plate.</p>
| + | |
− | <p>And grow up at 37 degree for 10-12 hours.</p>
| + | |
− | <h5>2016.06.10</h5>
| + | |
− | <p>Extracted the plasmid, and measure the concentration.</p>
| + | |
− | <p>Stored the plasmid at -20 degree.</p>
| + | |
− | | + | |
− | </div>
| + | |
− | <div class="col-md-3">
| + | |
− | <ul id="sidemenu">
| + | |
− | <li><a href="#" onclick="toEvent('section1');">Section 1</a></li> | + | |
− | <li><a href="#" onclick="toEvent('section2');">Section 2</a></li> | + | |
− | </ul> | + | |
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