Difference between revisions of "Team:UChicago/Basic Part"

 
Line 11: Line 11:
  
  
<p><span class="ptitle"> Our plasmid contains both GAL4-KaiC fusion protein and a KaiB protein, linked by a self-cleaving linker:</span></p>
+
<p><span class="ptitle"> Our submitted plasmid contains both GAL4-KaiC fusion protein and a KaiB protein, linked by a self-cleaving linker:</span></p>
 
<br>
 
<br>
 
<div class="content">
 
<div class="content">
Line 19: Line 19:
 
<span class="ptitle"><a href="http://parts.igem.org/Part:BBa_K2176002">BBa_K2176002</a></span><br><br>
 
<span class="ptitle"><a href="http://parts.igem.org/Part:BBa_K2176002">BBa_K2176002</a></span><br><br>
 
<p><span class="p">
 
<p><span class="p">
This plasmid contains KaiC fused to a Gal4 activation domain, with a self-cleaving peptide linker, P2A, fusing it to KaiB. P2A cleaves itself during translation, causing the KaiC-Gal4AD and the KaiB to separate. We did this to allow us to control the exact ratio of KaiC, KaiB, and KaiA, and make sure it is constant and equal in every cell. It is also codon optimized for yeast, and contains an NLS sequence to localize it to the nucleus. This part was synthesized by Genscript.</span></p>
+
The plasmid we submitted to the iGEM registry contains KaiC fused to a Gal4 activation domain, with a self-cleaving peptide linker, P2A, fusing it to KaiB. P2A cleaves itself during translation, causing the KaiC-Gal4AD and the KaiB to separate. We did this to allow us to control the exact ratio of KaiC, KaiB, and KaiA, and make sure it is constant and equal in every cell. It is also codon optimized for yeast, and contains an NLS sequence to localize it to the nucleus. This part was synthesized by Genscript.</span></p>
  
 
     </div>
 
     </div>

Latest revision as of 01:12, 20 October 2016

Our submitted plasmid contains both GAL4-KaiC fusion protein and a KaiB protein, linked by a self-cleaving linker:


BBa_K2176002

The plasmid we submitted to the iGEM registry contains KaiC fused to a Gal4 activation domain, with a self-cleaving peptide linker, P2A, fusing it to KaiB. P2A cleaves itself during translation, causing the KaiC-Gal4AD and the KaiB to separate. We did this to allow us to control the exact ratio of KaiC, KaiB, and KaiA, and make sure it is constant and equal in every cell. It is also codon optimized for yeast, and contains an NLS sequence to localize it to the nucleus. This part was synthesized by Genscript.