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 valign="top"><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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Revision as of 14:55, 15 October 2014
System Design |
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