Difference between revisions of "Team:William and Mary/Interlab"

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Interlab
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<h3 style='padding-top: 50px; padding-bottom: 50px;'>Advisors</h3>
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We participated in the Interlab Measurement Study using Flow Cytometry analysis on a FACS (Fluorescence-Activated Cell Sorter)
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machine following the protocol provided by iGEM. Our results are presented here:
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In addition to participating in the Interlab Study, we also wanted to determine if there would be a noticeable difference
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between measurements taken at Midlog and measurements taken on those same samples at Saturation.
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We noticed that although there were differences between the midlog and saturation measurements, they were not very drastic
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across the different devices when looking at bulk population-level mean measurements, with the exception of the negative control.
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However, because we measured the devices with flow cytometry, we were additionally able to assess the changes in population
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heterogeneity which occur with between midlog phase and saturation phase. We found that the midlog populations tended to be more
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unimodal than the saturation populations.
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Fig. 3: Representative single-cell histograms of absolute fluorescence levels for the same sample at midlog phase vs. at saturation phase
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A possible explanation for this phenomenon is that the antibiotic selection for the reporter construct may weaken over time,
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allowing subpopulations of cells to develop which have varying metabolic emphases on the reporter construct.
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All of the FACS plots from our Interlab study are available upon request.
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Revision as of 18:20, 27 June 2017