Team:Slovenia/METHODS and PARTS/notebook/viola

From 2010.igem.org

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<a href="/Team:Slovenia/METHODS_and_PARTS/notebook"><span id="stopnja3" >Split/FRET</span></a>
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<a href="/Team:Slovenia/METHODS_and_PARTS/notebook/oscil"><span id="stopnja3">Oscillator</span></a>
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<a href="/Team:Slovenia/METHODS_and_PARTS/notebook/oscil"><span id="stopnja3">oscillator</span></a>
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<a href="/Team:Slovenia/METHODS_and_PARTS/notebook/viola"><span id="stopnja3a" margin-left:15px;">Violacein</span></a>
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Latest revision as of 21:36, 27 October 2010

Fun fact:

notebook - violacein


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8/9/2010-8/15/2010

 

DH5α cells were transformed with three plasmids (taken from the Registry) containing the violacein operon. ([http://partsregistry.org/wiki/index.php/Part:BBa_K274002 BBa_K274002], [http://partsregistry.org/wiki/index.php/Part:BBa_K274003 BBa_K274003],[http://partsregistry.org/wiki/index.php/Part:BBa_K274004 BBa_K274004]). The cells were grown on LB Kan/Tc agar plates. Transformation of part Bba_K274002 was unsuccessful – there were no colonies on the LB Tc plates. Colonies containing plasmids with parts BBa_K274003 and BBa_K274004 were later inoculated into mini-prep flasks with Kan. Plasmid DNA was isolated from the over-night cultures.

 

Primers for amplificiation of separate vio genes were designed and ordered, and a table of constructs, necessary for the experiment was made.