Difference between revisions of "Team:Cambridge-JIC/Design"
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<h2>Problem statement</h2> | <h2>Problem statement</h2> | ||
− | <p>The use of fluorescent markers is central to many iGEM projects. In fact, the most widely used coding BioBrick on the iGEM Parts Registry is that encoding GFP, with 514 uses. However, the tool generally used to characterise a construct’s fluorescence - a fluorescence microscope - is prohibitively expensive for most iGEM teams, costing over $30,000.</p> | + | <!--<p>The use of fluorescent markers is central to many iGEM projects. In fact, the most widely used coding BioBrick on the iGEM Parts Registry is that encoding GFP, with 514 uses. However, the tool generally used to characterise a construct’s fluorescence - a fluorescence microscope - is prohibitively expensive for most iGEM teams, costing over $30,000.</p> |
− | <p>Therefore the problem we set out to tackle was <i> to design a cost-effective but precise method of quantifying fluorescence from the fluorescent proteins most commonly used in iGEM. </i></p> | + | <p>Therefore the problem we set out to tackle was <i> to design a cost-effective but precise method of quantifying fluorescence from the fluorescent proteins most commonly used in iGEM. </i></p>--> |
− | </ | + | <p>Microscopy allows us to visualise the world of synthetic biology. The high cost of commercial microscopes creates a barrier between the population and exploring biology visually. By creating a </p> |
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Revision as of 01:45, 16 September 2015
Problem statement
Microscopy allows us to visualise the world of synthetic biology. The high cost of commercial microscopes creates a barrier between the population and exploring biology visually. By creating a