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Our engineered bacteria successfully characterized Bcam0581. And it was proved that the BDSF produced by Bcam0581 was effective in inhibiting <em>C. albicans</em> phase transformation. | Our engineered bacteria successfully characterized Bcam0581. And it was proved that the BDSF produced by Bcam0581 was effective in inhibiting <em>C. albicans</em> phase transformation. | ||
− | Click BBa_K3078003 or Result to learn more. | + | Click <a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3078003">BBa_K3078003</a> or <a href="https://2019.igem.org/Team:Jilin_China/Result">Result</a> to learn more. |
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− | This year, a promoter strength measurement intermediate (BBa_K3078100) was created by Jilin_China. This part consists of two BbsI digestion sites, RBS and sfGFP. | + | This year, a promoter strength measurement intermediate (<a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K3078100">BBa_K3078100</a>) was created by Jilin_China. This part consists of two BbsI digestion sites, RBS and sfGFP. |
Testing promoter strength becomes very convenient through our part. Promoter with BbsI enzyme cutting site can be assembled to the measuring element by GoldenGate assambly. This construction assambly does not produce any scar and ensures that the RBS and fluorescent protein sequences are completely identical except for the promoter. | Testing promoter strength becomes very convenient through our part. Promoter with BbsI enzyme cutting site can be assembled to the measuring element by GoldenGate assambly. This construction assambly does not produce any scar and ensures that the RBS and fluorescent protein sequences are completely identical except for the promoter. |
Revision as of 01:56, 22 October 2019
Team
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