Difference between revisions of "Team:Newcastle/InterLab Results"

 
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<h1>Plate Reader Results</h1>
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<h3>Absorbance Values at 600 nm</h3>
 
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<h1>Flow Cytometry Results</h1>
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<h3>Calibration Particles Peak and Mean Conversion Values</h3>
 
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<p><figcaption>Figure 1. Recorded OD600 values as noted in the provided Interlab Excel data sheet </figcaption></figure></p>
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<p><figcaption>Figure 7. SpheroTech RCP-30-5A Rainbow Calibration Particles were used to obtain mean conversion values.</figcaption></figure></p>
 
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<h3>Geometric Mean MEFL of Negative and Positive Controls and 3 Devices</h3>
 
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<p><figcaption>Figure 1. Recorded OD600 values as noted in the provided Interlab Excel data sheet </figcaption></figure></p>
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<p><figcaption>Figure 8. Geometric mean MEFL values were calculated by measuring the number of events and geometric mean values in 5 samples and using mean conversion value from the table above.</figcaption></figure></p>
 
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Latest revision as of 22:22, 19 October 2016


Plate Reader Results



Absorbance Values at 600 nm

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Figure 1. Recorded OD600 values as noted in the provided Interlab Excel data sheet


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Figure 2. OD600 values plotted as a graph


Fluorescence values

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Figure 3. Recorded OD600 values as noted in the provided Interlab Excel data sheet


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Figure 4. OD600 values plotted as a graph


Normalised Fluorescence/OD600 values

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Figure 5. Recorded OD600 values as noted in the provided Interlab Excel data sheet


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Figure 6. OD600 values plotted as a graph


Flow Cytometry Results



Calibration Particles Peak and Mean Conversion Values

some text

Figure 7. SpheroTech RCP-30-5A Rainbow Calibration Particles were used to obtain mean conversion values.


Geometric Mean MEFL of Negative and Positive Controls and 3 Devices

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Figure 8. Geometric mean MEFL values were calculated by measuring the number of events and geometric mean values in 5 samples and using mean conversion value from the table above.