Difference between revisions of "Team:NYMU-Taipei/Parts"

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<p>This group ranges from <a>part BBa_K275001</a> to <a>BBa_K275007</a>. The parts are the ones that we primarily constructed and utilized in the FRET system. <a>BBa_K275001</a> is a pET32a with its MCS replaced with sequences designed by us. The replacement sequence contains a specifically designed MCS that can be inserted with a FRET protein and a DKK1-binding protein and express the two proteins as a fusion protein under the control of lac operon of pET32a. Hence, <a>part BBa_K275003</a> to <a>part BBa_K275007</a> are all cloned using BBa_K275001.</p>
 
<p>This group ranges from <a>part BBa_K275001</a> to <a>BBa_K275007</a>. The parts are the ones that we primarily constructed and utilized in the FRET system. <a>BBa_K275001</a> is a pET32a with its MCS replaced with sequences designed by us. The replacement sequence contains a specifically designed MCS that can be inserted with a FRET protein and a DKK1-binding protein and express the two proteins as a fusion protein under the control of lac operon of pET32a. Hence, <a>part BBa_K275003</a> to <a>part BBa_K275007</a> are all cloned using BBa_K275001.</p>
  
<h2>1. The Submitted Parts</h2>
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<h2>2. The Submitted Parts</h2>
<p>Ranging from <a>BBa_K275008</a> to <a>BBa+K275015</a> are the parts that we sent for the medal criteria. Since we have establish a system that is suitable for our project but completely different from RFC 10 regulations this year, we can only submit a portion of the parts we have created or there would be too many point mutations to make. While all of them except mEGFP, which is assigned as the improved part, are functional and eligible for silver medal's new part criteria, <a>BBa_K275013</a> stood out as our favorite composite part and <a>BBa_K275015</a> is our favorite basic part.</p>
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<p>Ranging from <a>BBa_K275008</a> to <a>BBa+K275015</a> are the parts that we sent for the medal criteria. Since we have establish a system that is suitable for our project but completely different from RFC 10 regulations this year, we can only submit a portion of the parts we have created or there would be too many point mutations to make. While all of them except mEGFP, which is assigned as the improved part, are functional and eligible for silver medal's validated part criteria, <a>BBa_K275013</a> stood out as our favorite composite part and <a>BBa_K275015</a> is our favorite basic part.</p>
 
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<h2>3. The plasmids for Cell Model</h2>
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<p>The Cell Model has 4 major contructs: from <a>BBa_K275024</a> to <a>BBa_K275027</a>. They are the plasmids that are transformed into HEK293 and DP for fluorescence exhibition.</p>
 
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<groupparts>iGEM18 NYMU-Taipei</groupparts>
 
<groupparts>iGEM18 NYMU-Taipei</groupparts>

Revision as of 08:24, 14 October 2018




Parts Overview

This year, we constructed plenty of parts that can be categorized into 3 groups:

1. The plasmids for FRET Model

This group ranges from part BBa_K275001 to BBa_K275007. The parts are the ones that we primarily constructed and utilized in the FRET system. BBa_K275001 is a pET32a with its MCS replaced with sequences designed by us. The replacement sequence contains a specifically designed MCS that can be inserted with a FRET protein and a DKK1-binding protein and express the two proteins as a fusion protein under the control of lac operon of pET32a. Hence, part BBa_K275003 to part BBa_K275007 are all cloned using BBa_K275001.

2. The Submitted Parts

Ranging from BBa_K275008 to BBa+K275015 are the parts that we sent for the medal criteria. Since we have establish a system that is suitable for our project but completely different from RFC 10 regulations this year, we can only submit a portion of the parts we have created or there would be too many point mutations to make. While all of them except mEGFP, which is assigned as the improved part, are functional and eligible for silver medal's validated part criteria, BBa_K275013 stood out as our favorite composite part and BBa_K275015 is our favorite basic part.

3. The plasmids for Cell Model

The Cell Model has 4 major contructs: from BBa_K275024 to BBa_K275027. They are the plasmids that are transformed into HEK293 and DP for fluorescence exhibition.

<groupparts>iGEM18 NYMU-Taipei</groupparts>