Difference between revisions of "Part:BBa K1859016"
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<p>BBa_K1859016 can let mRNA circularize efficiently in E. coli by combining it with | <p>BBa_K1859016 can let mRNA circularize efficiently in E. coli by combining it with | ||
| − | <a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1859015" > BBa_K1859015 </a>. | + | <a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1859015" > [BBa_K1859015] </a>. |
</p> | </p> | ||
<p> | <p> | ||
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. | . | ||
The sequence that cloned extra in BBa_K1859016 has complementarity with the sequence that cloned extra in | The sequence that cloned extra in BBa_K1859016 has complementarity with the sequence that cloned extra in | ||
| − | <a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1859015" > BBa_K1859015</a>. | + | <a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1859015" > [BBa_K1859015]</a>. |
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<p> | <p> | ||
You can let mRNA circularize efficiently by using BBa_K1859016 and | You can let mRNA circularize efficiently by using BBa_K1859016 and | ||
| − | <a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1859015" > BBa_K1859015 </a> | + | <a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1859015" > [BBa_K1859015] </a> |
than using parts of 2014.( | than using parts of 2014.( | ||
<a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1332005" > [BBa_K1332005] </a> | <a href= "https://parts.igem.org/wiki/index.php?title=Part:BBa_K1332005" > [BBa_K1332005] </a> | ||
Revision as of 08:02, 22 September 2015
the 5´side of the intron[BBa_K1332003] +complementary seqence
BBa_K1859016 can let mRNA circularize efficiently in E. coli by combining it with [BBa_K1859015] .
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 of circular mRNA, refer to ‘iGEM Gifu 2014' .
We improved the 3´side of the intron [BBa_K1332005] of iGEM2014 and made BBa_K1859016. Circular parts of iGEM2014 are cloned only sequence of ribozyme involved the splicing from td intron in T4 phage. However, BBa_K1859016 is cloned the sequence except the ribozyme extra in addition to [BBa_K1332005] . The sequence that cloned extra in BBa_K1859016 has complementarity with the sequence that cloned extra in [BBa_K1859015].
You can let mRNA circularize efficiently by using BBa_K1859016 and [BBa_K1859015] than using parts of 2014.( [BBa_K1332005] and [BBa_K1332003] ).