Difference between revisions of "Part:BBa K2703002:Experience"

 
(Applications of BBa_K2703002)
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===Applications of BBa_K2703002===
 
===Applications of BBa_K2703002===
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Our part is compatible with the PhytoBrick MoClo standard. This PhytoBrick was intented to be use as constitutive promoter for the transcription unit of paromomycine in the CARGO of our synthetic retrotransposons for directed evolution on the Chlamydomoas. It is part of our reporter system to characterize the activity and transposition rate.
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<br> <br>
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We couldn’t directly use our Phytobrick for the characterisation because we didn’t have time to construct all the other that are needed for the final assembly. Instead we use a slightly different Phytobrick with the same P PSAD. sequence but with one different fusion site. This part was assembled in a functional Transcription Unit with the resistance gene paromomycine that
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was as a reporter gene. After transformation in C.reinhardtii D66 the functionality of the promoter was tested by counting the number of chlamydomonas colony resistant to paromomycine (15 ug/ml). Different constructions were made to characterize and compare the functionality of P pSAD . We tested different combination of promoters and 3’UTR.
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<table> 
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  <tbody>     
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  <tr>
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  <td>Literrature researches</td>
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  <td>Whole team participated.</td>
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  </tr>
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  <tr >
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  <td></td>
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  <td></td>
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<td></td>
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  <td></td>
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<td></td>
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  <td></td>
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<td></td>
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  <td></td>
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<td></td>
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  <td></td>
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  </tr>
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  <tr>
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  <td> Protocols </td>
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  <td>Aurélie Bouin </td>
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  </tr>
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  <tr>
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  <td>Shipping lab materials</td>
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  <td>Lucas Leonardi, Saniya Kari</td>
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  </tr>
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  <tr>
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  <td>Interlab </td>
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  <td>Ursula Saade, Asmaa Foda and Dounia Chater</td>
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  </tr>
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  <tr>
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  <td>"Safety form  </td>
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    <td>Aurélie Bouin and Saniya Kari</td>
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  </tr>
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  <tr>
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  <td>Modelisation</td>
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  <td>Victor Sayous, Ursula Saade, Charlotte Bellamy </td>
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  </tr>
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  </tbody>
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</table>
  
 
===User Reviews===
 
===User Reviews===

Revision as of 14:41, 9 October 2018


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_K2703002

Our part is compatible with the PhytoBrick MoClo standard. This PhytoBrick was intented to be use as constitutive promoter for the transcription unit of paromomycine in the CARGO of our synthetic retrotransposons for directed evolution on the Chlamydomoas. It is part of our reporter system to characterize the activity and transposition rate.

We couldn’t directly use our Phytobrick for the characterisation because we didn’t have time to construct all the other that are needed for the final assembly. Instead we use a slightly different Phytobrick with the same P PSAD. sequence but with one different fusion site. This part was assembled in a functional Transcription Unit with the resistance gene paromomycine that was as a reporter gene. After transformation in C.reinhardtii D66 the functionality of the promoter was tested by counting the number of chlamydomonas colony resistant to paromomycine (15 ug/ml). Different constructions were made to characterize and compare the functionality of P pSAD . We tested different combination of promoters and 3’UTR.

<tbody> </tbody>
Literrature researches Whole team participated.
Protocols Aurélie Bouin
Shipping lab materials Lucas Leonardi, Saniya Kari
Interlab Ursula Saade, Asmaa Foda and Dounia Chater
"Safety form Aurélie Bouin and Saniya Kari
Modelisation Victor Sayous, Ursula Saade, Charlotte Bellamy

User Reviews

UNIQdeff87ca9ee07e80-partinfo-00000000-QINU UNIQdeff87ca9ee07e80-partinfo-00000001-QINU