Difference between revisions of "Team:CCU Taiwan/Parts"

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         <section id="ove">
 
         <section id="ove">
 
             <h2>Overview</h2>
 
             <h2>Overview</h2>
             <p></p>
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             <p>With linear array epitope technique, we have produced various length of tandem-repeated sequence, but we need the sequences which are long enough to ensure that we have enough productivity. The plasmids we used to express protein are pET-29a(+) and pET-29b(+), where T7 promoter and lac operator would be induced with IPTG. On the other hand, there are also 6X His tag on pET-29a(+) and pET-29b(+) to purify our target proteins. Furthermore, we produced E protein to do the binding affinity test and CLEC5A to be our control.
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Our parts are as follows:</p>
 
         </section>
 
         </section>
 
         <br>
 
         <br>
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                     <tr>
 
                     <tr>
 
                         <td><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3648009" target="_blank">BBa_K3648009</a></td>
 
                         <td><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3648009" target="_blank">BBa_K3648009</a></td>
                         <td>TRS-110R*7</td>
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                         <td>Thrombin site</td>
 
                         <td>16</td>
 
                         <td>16</td>
 
                     </tr>
 
                     </tr>
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         <br>
 
         <br>
 
         <section id="com">
 
         <section id="com">
             <h2Composite Parts</h2>
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             <h2>Composite Parts</h2>
 
             <table>
 
             <table>
 
                 <tbody>
 
                 <tbody>
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                     <tr>
 
                     <tr>
 
                         <td><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3648003" target="_blank">BBa_K3648003</a></td>
 
                         <td><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3648003" target="_blank">BBa_K3648003</a></td>
                         <td>pET29b(+)-CLEC5A</td>
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                         <td>pET-29b(+)_CLEC5A</td>
 
                         <td>655</td>
 
                         <td>655</td>
 
                     </tr>
 
                     </tr>
 
                     <tr>
 
                     <tr>
 
                         <td><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3648004" target="_blank">BBa_K3648004</a></td>
 
                         <td><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3648004" target="_blank">BBa_K3648004</a></td>
                         <td>pET29A(+)-E protein</td>
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                         <td>pET-29a(+)_E protein</td>
 
                         <td>1687</td>
 
                         <td>1687</td>
 
                     </tr>
 
                     </tr>
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                     <tr>
 
                     <tr>
 
                         <td><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3648013" target="_blank">BBa_K3648013</a></td>
 
                         <td><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3648013" target="_blank">BBa_K3648013</a></td>
                         <td>pET-29b(+)_TRS-151*7</td>
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                         <td>pET-29b(+)_TRS-151*8</td>
 
                         <td>414</td>
 
                         <td>414</td>
 
                     </tr>
 
                     </tr>
 
                     <tr>
 
                     <tr>
 
                         <td><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3648015" target="_blank">BBa_K3648015</a></td>
 
                         <td><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3648015" target="_blank">BBa_K3648015</a></td>
                         <td>pET-29b(+)-TRS-151*7</td>
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                         <td>pET-29b(+)_TRS-151*7</td>
 
                         <td>384</td>
 
                         <td>384</td>
 
                     </tr>
 
                     </tr>

Latest revision as of 14:48, 26 October 2020

Parts

Overview

With linear array epitope technique, we have produced various length of tandem-repeated sequence, but we need the sequences which are long enough to ensure that we have enough productivity. The plasmids we used to express protein are pET-29a(+) and pET-29b(+), where T7 promoter and lac operator would be induced with IPTG. On the other hand, there are also 6X His tag on pET-29a(+) and pET-29b(+) to purify our target proteins. Furthermore, we produced E protein to do the binding affinity test and CLEC5A to be our control. Our parts are as follows:


Basic Parts

Part Number Description Length (bp)
BBa_R0187 T7 promoter (lac Irepressible) 44
BBa_K2549058 HA tag 27
BBa_K3183024 HA Tag for L.reuteri 27
BBa_K2382008 6X His Tag 18
BBa_M10045 Myc Tag 30
BBa_K3648001 C-type lectin domain family 5 member A 483
BBa_K3648002 Envelope protien 1485
BBa_K3648005 TRS-110*3 102
BBa_K3648006 TRS-151*8 243
BBa_K3648007 TRS-110R*7 255
BBa_K3648008 S-tag 45
BBa_K3648009 Thrombin site 16
BBa_K3648010 T7 terminator 48
BBa_K3648014 TRS-151*7 213

Composite Parts

Part Number Description Length (bp)
BBa_K3648003 pET-29b(+)_CLEC5A 655
BBa_K3648004 pET-29a(+)_E protein 1687
BBa_K3648011 pET-29b(+)_TRS-110*3 313
BBa_K3648012 pET-29b(+)_TRS-110R*7 466
BBa_K3648013 pET-29b(+)_TRS-151*8 414
BBa_K3648015 pET-29b(+)_TRS-151*7 384