Team:TCU Taiwan/SystemDesign
From 2014.igem.org
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<td><font size="3" face="Verdana" color="#333"><p>After constructed our CRISPR system, we ligated it with a red fluorescent reporter gene (<a href="http://parts.igem.org/Part:BBa_I13521" target="_blank">BBa_I13521</a>), so once our system is spread, all bacterium get this system will become red. Finally, we put whole system into phagemid pBluescript II SK(-), and get the recombinant phagemid for M13 infection.</p></font></td> | <td><font size="3" face="Verdana" color="#333"><p>After constructed our CRISPR system, we ligated it with a red fluorescent reporter gene (<a href="http://parts.igem.org/Part:BBa_I13521" target="_blank">BBa_I13521</a>), so once our system is spread, all bacterium get this system will become red. Finally, we put whole system into phagemid pBluescript II SK(-), and get the recombinant phagemid for M13 infection.</p></font></td> | ||
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<td><img src="https://static.igem.org/mediawiki/2014/4/4b/TCU_SD_10572757_390371167783707_1137689428_o.jpg" width="100%" /></td> | <td><img src="https://static.igem.org/mediawiki/2014/4/4b/TCU_SD_10572757_390371167783707_1137689428_o.jpg" width="100%" /></td> |
Revision as of 14:52, 15 October 2014
System Design |
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