Difference between revisions of "Team:Tianjin/Measurement"

 
Line 433: Line 433:
 
         </div>
 
         </div>
  
                                <div class="col-xs-12 text">
+
                             
                                    <p>Some basic information can be gained from the above figures:</p>
+
                                    <ol>
+
                                        <li>Compared with the corresponding control groups, all the experimental groups have showed apparent oscillatory signals.</li>
+
                                        <li>In the measured 3500 min, the oscillations in 700-2000 min are extremely unstable and nearly absent, while the oscillations for the rest of the time are relatively stable.</li>
+
                                        <li>The cycle is about 500min (about 8.3h).</li>
+
                                    </ol>
+
                                    <p><strong><strong>Note: final measurement results and analysis should be accessed in <a href="https://2018.igem.org/Team:Tianjin/Demonstrate">Demonstrate</a> page.</strong></strong></p>
+
                                </div>
+
 
                             </div>
 
                             </div>
 
                         </div>
 
                         </div>

Latest revision as of 13:47, 13 December 2018

<!DOCTYPE html> Team:Tianjin - 2018.igem.org

MEASUREMENT

In pursuit of a rigorously scientific result, we have adopted multiple measuring approaches throughout the whole project, among which two predominant methods described in extreme detail in wiki, would inspire relative researchers.

As two sophisticated and renowned reporters in biotechnological domain, fluorescent protein and luciferase were opted to illustrate the effectiveness of our constructed oscillating system, detected by combined means and instrument. Mcherry and EYFP, two selected fluorescent reporters were measured by both fluorescence spectrophotometer and Leica DMi8 respectively. Leica DMi8 allows us to visually and intuitively see the expression of the fluorescent protein EYFP in Saccharomyces cerevisiae In terms of luciferase, in addition to commonly used firefly luciferase, a courageous attempt we made was to choose a novel luciferase NanoLuc and its live cell substrate in spite of no records of the usefulness in Saccharomyces cerevisiae before and obtained expected outcome successfully.