Difference between revisions of "Team:Aalto-Helsinki"

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<div class="title_style animate_title" id="title3"><br> Our Lab</div>

<div class="title_style animate_title" id="title3"><br> Our Lab</div>

<div class="text_style"><br><br> <p>The parts of our fusion proteins were ordered as separate sequences: mRPF, Prancer Purple, sgBP, silk repeats, cellulose binding module, and keratin binding domain. Constructs containing a chromoprotein sequence, a binding domain, and silk repeats in different combinations were assembled with Golden Gate. Purified and evaluated plasmids were transformed in <i>E. coli</i> production strain BL21, and the constructs were produced by inducing with IPTG. Proteins were purified with ÄKTA or a heat-based protocol based on our modeling results.</p>

<div class="text_style"><br><br> <p>The parts of our fusion proteins were ordered as separate sequences: mRPF, Prancer Purple, sgBP, silk repeats, cellulose binding module, and keratin binding domain. Constructs containing a chromoprotein sequence, a binding domain, and silk repeats in different combinations were assembled with Golden Gate. Purified and evaluated plasmids were transformed in <i>E. coli</i> production strain BL21, and the constructs were produced by inducing with IPTG. Proteins were purified with ÄKTA or a heat-based protocol based on our modeling results.</p>

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<li>The production of colorful silk fibers.</li>

<li>The production of colorful silk fibers.</li>

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