From 2014.igem.org
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| - | <h1>Lab Book</h1>
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| - | <h1>Part A</h1>
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| - | <h1>Part B</h1>
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| - | <h2> Week 1 </h2>
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| - | <p> <font style="font-weight:bold">Tasks completed:</font>
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| - | Swapping resistance gene for plasmid pME6010 from tetracycline to kanamycin. <br><br>
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| - | <font style="font-weight:bold">Methods:</font>
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| - | First, we designed forward and reverse primers for KanR (with native RSB and promoter) which we isolated from plasmid pCM66. The 5’ ends were complementary to the insert region of pME6010 (reaction 1).
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| - | We then designed forward and reverse primers to amplify the pME6010 backbone (reaction 2).
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| - | Further to this we redesigned each set of primers to incorporate an ampicillin promoter and optimised RBS (https://salis.psu.edu/software/) (B reactions) instead of the native promoter region (A reactions).
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| - | The designed plasmids were as follows:
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| - | <h1>Part C</h1>
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Latest revision as of 01:03, 18 October 2014
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