Team:Goettingen/week21-2
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- | <h2><b> | + | <h2><b>V09_17 </b></h2><br> |
- | <b> | + | <b>Preparative double digestion of flhDC, FliC, 18K-RFP and Psb1c3 followed by ligation</i></b><br> |
<ul> | <ul> | ||
<li>Experiment: <br> | <li>Experiment: <br> | ||
- | + | In order to clone the flhDC, FliC and 18K-RFP constructs into pSB1C3, all components were digested with EcoRI and PstI according to the <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>. The restriction products were subsequently separated on a gel in order to verify the digestions success and purify the desired fragments. After measuring the concentration of the purified fragments, an overnight ligation was initiated .<br> | |
<br> | <br> | ||
</li> | </li> |
Revision as of 07:22, 18 September 2012
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#2 Speed Improvement - 21st weekBack to overview
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