Difference between revisions of "Team:NCTU Formosa/Composite Part"
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+ | <div class="p01"> | ||
+ | <div class="background1"></div> | ||
+ | <div class="title">Composite Parts</div> | ||
</div> | </div> | ||
+ | <div class="p02"> | ||
+ | <div class="content"> | ||
+ | <h2>Composite Part</h2> | ||
− | < | + | <table> |
− | + | <tr><td width="20%"></td><td width="13%"></td><td width="67%"></td></tr> | |
− | </ | + | |
− | < | + | <tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694013">BBa_K1694013</a></span><br> |
+ | OmpA-anti-VEGF<br> | ||
+ | <span><a href="http://parts.igem.org/Part:BBa_K1694014">BBa_K1694014</a></span><br> | ||
+ | OmpA-anti-EGFR<br> | ||
+ | <span><a href="http://parts.igem.org/Part:BBa_K1694015">BBa_K1694015</a></span><br> | ||
+ | OmpA-anti-HER2<br> | ||
+ | </td><td></td><td>In order to change the scFv parts easily, we added a <i>Nco</i>I restriction site between OmpA and scFv so that we can change various scFv DNA sequence using the <i>Nco</i>I restriction enzyme.</td></tr> | ||
+ | <tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694023">BBa_K1694023</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+OmpA-anti-VEGF<br> | ||
+ | <span><a href="http://parts.igem.org/Part:BBa_K1694024">BBa_K1694024</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+OmpA-anti-EGFR<br> | ||
+ | <span><a href="http://parts.igem.org/Part:BBa_K1694025">BBa_K1694025</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+OmpA-anti-HER2<br> | ||
+ | </td><td></td><td>By ligating the constitutive promoter (<a href="http://parts.igem.org/Part:BBa_J23101">BBa_J23101</a>), strong ribosome binding site (<a href="http://parts.igem.org/Part:BBa_B0034">BBa_B0034</a>) and Lpp-OmpA-scFv, we were able to display scFv on the <i>E.coli</i> outer membrane continuously. | ||
+ | Having this part, we can co-transform with other parts in order to produce color as the detection signal.<br><br> | ||
+ | In addition, by co-transforming these different types of <i>E.coli</i> with different fluorescence or color as signals, we are able to create a platform which can detect multimarker and consequently achieve combination therapy. | ||
+ | </td></tr> | ||
+ | |||
+ | <tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694033">BBa_K1694033</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+OmpA-anti-VEGF+RBS+GFP+Ter<br> | ||
+ | <span><a href="http://parts.igem.org/Part:BBa_K1694034">BBa_K1694034</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+OmpA-anti-EGFR+RBS+GFP+Ter<br> | ||
+ | <span><a href="http://parts.igem.org/Part:BBa_K1694035">BBa_K1694035</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+OmpA-anti-HER2+RBS+GFP+Ter<br> | ||
+ | <span><a href="http://parts.igem.org/Part:BBa_K1694044">BBa_K1694044</a></span><br> | ||
+ | Pcons+RBS+OmpA-anti-EGFR+RBS+RFP+Ter<br> | ||
+ | <span><a href="http://parts.igem.org/Part:BBa_K1694045">BBa_K1694045</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+OmpA-anti-HER2+RBS+BFP+Ter<br> | ||
+ | |||
+ | </td><td></td><td>The most commonly constructing way of composite parts is to ligate the required parts together. We also provide this kind of parts.<br> | ||
+ | At the back of the Lpp-OmpA-scFv part, we ligated the weaker ribosome biding site (<a href="網址">BBa_B0030</a>), different fluorescent protein and terminator (<a href="http://parts.igem.org/Part:BBa_J61048">BBa_J61048</a>) to make it continuously and simultaneously express the fluorescence and the scFv. We used a weak ribosome binding site to ensure that scFv's production will not be affected. | ||
+ | </td></tr> | ||
+ | |||
+ | <tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694053">BBa_K1694053</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+OmpA-anti-VEGF+RBS+amilCP+Ter<br> | ||
+ | <span><a href="http://parts.igem.org/Part:BBa_K1694054">BBa_K1694054</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+OmpA-anti-EGFR+RBS+amilCP+Ter<br> | ||
+ | <span><a href="http://parts.igem.org/Part:BBa_K1694055">BBa_K1694055</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+OmpA-anti-HER2+RBS+amilCP+Ter<br> | ||
+ | </td><td></td><td>Chromoprotein is another example of what can be added when making your own probe.<br> | ||
+ | We constructed this part as the P<sub>cons</sub>+RBS+OmpA-scFv+RBS+fluorescent protein+Terminator part. | ||
+ | </td></tr> | ||
+ | |||
+ | <tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694027">BBa_K1694027</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+FadL-GBP<br> | ||
+ | </td><td></td><td>By ligating the induced promoter (<a href="http://parts.igem.org/Part:BBa_J23110">BBa_J23110</a>), ribosome binding site (<a href="http://parts.igem.org/Part:BBa_B0034">BBa_B0034</a>) and FadL-GBP, we can continuously display the GBP on the <i>E.coli</i> outer membrane.<br> | ||
+ | Then we co-transform the OmpA-scFv parts and this FadL-GBP parts into the same <i>E.coli</i>, hence allowing our <i>E.coli</i> to bind on gold chips and detect antigens simultaneously. | ||
+ | </td></tr> | ||
+ | |||
+ | <tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694037">BBa_K1694037</a></span><br> | ||
+ | P<sub>cons</sub>+RBS+FadL-GBP+RBS+GFP+Ter<br> | ||
+ | </td><td></td><td>With this part, we can test the GBP function by observing the green fluorescence on the gold chip. Terminator is (<a href="http://parts.igem.org/Part:BBa_B0015">BBa_B0015</a>). | ||
+ | </td></tr> | ||
+ | |||
+ | </table> | ||
</div> | </div> | ||
+ | </div> | ||
+ | <div class="goto" style="background-color:#FCFCDE;"> | ||
+ | <a href="https://2015.igem.org/Team:NCTU_Formosa/Project"><img src="https://static.igem.org/mediawiki/2015/3/3c/%E7%AE%AD%E9%A0%AD1.png"; width=50vw;><br><br>Back to Navigation</a> | ||
+ | </div> | ||
+ | <div class="goto1" style="background-color:#FCFCDE;"> | ||
+ | <a href="https://2015.igem.org/Team:NCTU_Formosa/Practices"><img src="https://static.igem.org/mediawiki/2015/c/c2/%E7%AE%AD%E9%A0%AD2.png"; width=50vw;><br><br>Go to Practices</a> | ||
+ | </div> | ||
+ | |||
+ | </body> | ||
</html> | </html> | ||
+ | |||
+ | {{Team:NCTU_Formosa/footer}} |
Latest revision as of 03:58, 19 September 2015
Composite Parts
Composite Part
BBa_K1694013 OmpA-anti-VEGF BBa_K1694014 OmpA-anti-EGFR BBa_K1694015 OmpA-anti-HER2 | In order to change the scFv parts easily, we added a NcoI restriction site between OmpA and scFv so that we can change various scFv DNA sequence using the NcoI restriction enzyme. | |
BBa_K1694023 Pcons+RBS+OmpA-anti-VEGF BBa_K1694024 Pcons+RBS+OmpA-anti-EGFR BBa_K1694025 Pcons+RBS+OmpA-anti-HER2 | By ligating the constitutive promoter (BBa_J23101), strong ribosome binding site (BBa_B0034) and Lpp-OmpA-scFv, we were able to display scFv on the E.coli outer membrane continuously.
Having this part, we can co-transform with other parts in order to produce color as the detection signal. In addition, by co-transforming these different types of E.coli with different fluorescence or color as signals, we are able to create a platform which can detect multimarker and consequently achieve combination therapy. | |
BBa_K1694033 Pcons+RBS+OmpA-anti-VEGF+RBS+GFP+Ter BBa_K1694034 Pcons+RBS+OmpA-anti-EGFR+RBS+GFP+Ter BBa_K1694035 Pcons+RBS+OmpA-anti-HER2+RBS+GFP+Ter BBa_K1694044 Pcons+RBS+OmpA-anti-EGFR+RBS+RFP+Ter BBa_K1694045 Pcons+RBS+OmpA-anti-HER2+RBS+BFP+Ter | The most commonly constructing way of composite parts is to ligate the required parts together. We also provide this kind of parts. At the back of the Lpp-OmpA-scFv part, we ligated the weaker ribosome biding site (BBa_B0030), different fluorescent protein and terminator (BBa_J61048) to make it continuously and simultaneously express the fluorescence and the scFv. We used a weak ribosome binding site to ensure that scFv's production will not be affected. | |
BBa_K1694053 Pcons+RBS+OmpA-anti-VEGF+RBS+amilCP+Ter BBa_K1694054 Pcons+RBS+OmpA-anti-EGFR+RBS+amilCP+Ter BBa_K1694055 Pcons+RBS+OmpA-anti-HER2+RBS+amilCP+Ter | Chromoprotein is another example of what can be added when making your own probe. We constructed this part as the Pcons+RBS+OmpA-scFv+RBS+fluorescent protein+Terminator part. | |
BBa_K1694027 Pcons+RBS+FadL-GBP | By ligating the induced promoter (BBa_J23110), ribosome binding site (BBa_B0034) and FadL-GBP, we can continuously display the GBP on the E.coli outer membrane. Then we co-transform the OmpA-scFv parts and this FadL-GBP parts into the same E.coli, hence allowing our E.coli to bind on gold chips and detect antigens simultaneously. | |
BBa_K1694037 Pcons+RBS+FadL-GBP+RBS+GFP+Ter | With this part, we can test the GBP function by observing the green fluorescence on the gold chip. Terminator is (BBa_B0015). |