Difference between revisions of "Part:BBa K1859011"

(Created page with "<html> <p>2(GGSGGS) linker+mRNA circularization device (3´ side)(endless)</p> <br> <p>This is Circular Parts conjuncted linker to keep folding of proteins.Circular Parts is wh...")
 
Line 1: Line 1:
 
<html>
 
<html>
−
<p>2(GGSGGS) linker+mRNA circularization device (3´ side)(endless)</p>
+
<p>2*GGSGGS linker+ The 5´side of the intron
 +
<a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1332003" > [BBa_K1332003]
 +
</a></p>
  
 
<br>
 
<br>
  
−
<p>This is Circular Parts conjuncted linker to keep folding of proteins.Circular Parts is what use sequence subcloned ribozyme involved self‐splicing in T4 Phage.By associating Circular Parts, 3'intron parts and 5'intron parts, on both ends of optional sequwnce, you can circularize mRNA making its DNA. </p>
+
<p>BBa_K1859011 is the 5'side of the intron
 +
<a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1332003" > [BBa_K1332003] </a>
 +
conjuncted linker to keep folding of proteins.
 +
 
 +
Circular Parts, the 3'side of the intron
 +
<a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1332005" > [BBa_K1332005] </a>
 +
and the 5'side of the intron
 +
<a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1332003" > [BBa_K1332003] </a>
 +
, is what use sequence subcloned ribozyme involved self‐splicing in T4 Phage.
 +
 
 +
By associating Circular Parts on both ends of optional sequence, you can circularize mRNA making its DNA. </p>
 +
 
 
<p>As for details, refer to  
 
<p>As for details, refer to  
 
<a href= "http://2014.igem.org/Team:Gifu" > iGEM Gifu 2014 </a>
 
<a href= "http://2014.igem.org/Team:Gifu" > iGEM Gifu 2014 </a>
Line 10: Line 23:
  
 
<br>
 
<br>
−
<p>In the study of iGEM Gifu 2014, we made long-chain protein from cyclic mRNA, but it lost functionality.It is thought that folding of the protein failed for a cause．Therefore we designed some linkers to fix the folding of the protein.These parts include sequence of Circular Parts and linker．The linker comes to be in the cyclic mRNA when mRNA is circularized.To make this device, we coupled the sequence of the linker, 2*GGSGGS , to the up stream of 5'intron.</p>
 
−
<p>The linker designed elsewhere is
 
−
<a href= "http://2015.igem.org/Team:Gifu/Result/" > here </a>.</p>
 
  
 +
<p>In the study of iGEM Gifu 2014, we made long-chain protein from Circular mRNA, but it lost functionality.
  
 +
It is thought that folding of the protein failed for a cause．
  
 +
Therefore we designed some linkers to fix the folding of the protein.
 +
 +
BBa_K1859011 includes sequence of the 5'side of the intron
 +
<a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1332003" > [BBa_K1332003] </a>
 +
and linker．
 +
 +
The linker comes inside the Circular mRNA when mRNA is circularized.
 +
 +
To make this device, we combined the sequence of the linker, 2*GGSGGS , to the upstream of 5'side of the intron
 +
<a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1332003" > [BBa_K1332003] </a>
 +
.</p>
 +
 +
<p>The linker designed elsewhere is
 +
<a href= "http://2015.igem.org/Team:Gifu/Result/" > here </a>.</p>
  
 
</html>
 
</html>

Revision as of 10:09, 16 September 2015

2*GGSGGS linker+ The 5´side of the intron [BBa_K1332003]


BBa_K1859011 is the 5'side of the intron [BBa_K1332003] conjuncted linker to keep folding of proteins. Circular Parts, the 3'side of the intron [BBa_K1332005] and the 5'side of the intron [BBa_K1332003] , is what use sequence subcloned ribozyme involved self‐splicing in T4 Phage. By associating Circular Parts on both ends of optional sequence, you can circularize mRNA making its DNA.

As for details, refer to iGEM Gifu 2014


In the study of iGEM Gifu 2014, we made long-chain protein from Circular mRNA, but it lost functionality. It is thought that folding of the protein failed for a cause． Therefore we designed some linkers to fix the folding of the protein. BBa_K1859011 includes sequence of the 5'side of the intron [BBa_K1332003] and linker． The linker comes inside the Circular mRNA when mRNA is circularized. To make this device, we combined the sequence of the linker, 2*GGSGGS , to the upstream of 5'side of the intron [BBa_K1332003] .

The linker designed elsewhere is here .