Team:Groningen/Template/MODULE/Notebook/secretion/week8
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- | + | Obtaining the anti-<i>Staphylococcus aureus</i> system (p2s) and the anti-<i>Pseudomonas aeruginosa</i> system(pLASs) | |
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- | A | + | <div class="item">Both systems were assembled by using Gibson assembly</div> |
- | + | <div class="item">Downstream of the <i>pLas</i> a RBS is attached together with the promoter P2 and <i>dspB</i> with tail PCR</div> | |
- | </div> | + | <div class="item">A Gibson tail was attached with PCR to the P2 with RBS, <i>dspB</i> with RBS, <i>aiiA</i> and the double terminator </div> |
+ | <div class="item">ssUSP45DspB, and <i>nisA</i> was added and incubated for 90 minutes at 50 °C</div> | ||
+ | <div class="item">The Gibson fragment was amplified with gradient PCR</div> | ||
+ | <div class="item">The construct was digested, checked on gel, and send for sequencing</div> | ||
+ | <div class="item">Only 1200 base pairs of the construct could be found on gel</div> | ||
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Latest revision as of 00:35, 18 October 2014
September 15 - September 19
Obtaining the anti-Staphylococcus aureus system (p2s) and the anti-Pseudomonas aeruginosa system(pLASs)
Both systems were assembled by using Gibson assembly
Downstream of the pLas a RBS is attached together with the promoter P2 and dspB with tail PCR
A Gibson tail was attached with PCR to the P2 with RBS, dspB with RBS, aiiA and the double terminator
ssUSP45DspB, and nisA was added and incubated for 90 minutes at 50 °C
The Gibson fragment was amplified with gradient PCR
The construct was digested, checked on gel, and send for sequencing
Only 1200 base pairs of the construct could be found on gel