Difference between revisions of "Team:Edinburgh UG/Collaborations"

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            <h2 style="text-align:left">Hosting Meetup with Newcastle team</h2>
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            <p style="text-align:left">If you have ever heard about the biggest world arts festival Fringe in Edinburgh, you probably know how crazy it gets. </p>
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             <h2 style="text-align:left">Results</h2>
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             <h2 style="text-align:left">Bits and pieces</h2>
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             <h2 style="text-align:left">Calibration</h2>
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             <p style="text-align:left">Besides meetups, labwork, we also had talks and chats with many other iGEM teams.  </p>
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             <h2 style="text-align:left">OD600 Reference Point</h2>
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             <p style="text-align:left">Absorbance of 0.051 of LUDOX CL-X was obtained with standard deviation of 0.005 while double distilled water had all four replicates at the same value of 0.034, implying that both measurements were done precisely.</p>
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             <h2 style="text-align:left">Mike the Microbe</h2>
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            <h2 style="text-align:left">Particle Standard Curve</h2>
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             <p style="text-align:left"> Picture </p>
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             <p style="text-align:left">Particle standard curve was obtained with R<sup>2</sup> value of 0.998 (Figure 1). However, logarithmic scale graph (Figure 2) represented less accurate measurement than linear curve (R<sup>2</sup>=0.993, red line), as linear graph was obtained only in high concentration of particles. Not very high precision may be due to the low absorbance values that is not in a plate reader range or when the absorbance is less than 0.1. Analysing the calibration curve in higher concentrations only, linear fit represented high accuracy in logarithmic scale with R<sup>2</sup>=0.998. </p>
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  <figcaption class="figure-caption">Figure 1. Particle standard curve obtained of a dilution series of monodisperse silica microspheres by measuring OD<sub>600</sub></figcaption>
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  <figcaption class="figure-caption">Figure 2. Particle standard curve (logarithmic scale) obtained of a dilution series of monodisperse silica microspheres by measuring OD<sub>600</sub> </figcaption>
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            <h2 style="text-align:left">Fluoresence Standard Curve</h2>
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            <p style="text-align:left">Fluoresence measurement may be considered as accurate as the data in both graphs (Figure 3 and Figure 4 for logarithmic scale) fit to a line with a value of R2 very close to 1. The slope on logarithmic scale is very close to 1 as well (slope = 0.969, Figure 4) which suggest that the data is considerably good. </p>
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  <figcaption class="figure-caption">Figure 3. Fluorescein standard curve obtained by making a series of dilutions of fluorescein</figcaption>
 
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  <figcaption class="figure-caption">Figure 4. Fluorescein standard curve obtained by making a series of dilutions of fluorescein (logarithmic scale) </figcaption>
 
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            <h2 style="text-align:left">Absorbance and fluorescence measurement using a plate reader </h2>
 
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            <p style="text-align:left">As the absorbance increased in time in all devices and both (positive and negative) controls (Figure 5), it suggests that cells grew in all devices during 6 hours time period, indicating that negative control grew slowest, then TD1 and TD4 grew slightly faster, while all the other devices were similar in the speed of growth. There is no significant relation between cells growth and fluorescence as an order of increasing absorbance or fluorescence varies among different test devices. As expected, negative control has no significant fluorescence. Least measurement of fluorescence was obtained in Test Device 4 and highest was obtained in Test Device 2.</p>
 
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  <figcaption class="figure-caption">Figure 5. FLuorescence and optical density measurement (600 nm) for all devices tested. </figcaption>
 
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            <p style="text-align:left">No correlation was observed among colony forming units (CFU) and absorption as only in the highest dilution factor (8 *10<sup>8</sup>) concentration of the overnight cultures  was countable (less than 300 colonies formed). </p>
 
 
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Revision as of 15:34, 16 October 2018

Edinburgh iGEM 2018

Collaborations

Let's do something together!

Collaboration in science is one of the most important steps to succeed. You are very good at your field but struggling in the other? It is not a problem at all when you are open and you are not afraid to ask for help or you can help someone. Meeting other people while doing a science project is also essential. Other people with their fresh mind might easily notice why something may go wrong, suggest new ideas or just share their opinion. So, let's collaborate!

Meetups

As one of the most important collaborations we attendend two meetups and hosted one as well.

iGEM UK Meetup

As our first meetup we attended iGEM meetup UK which was organised by SynBioUK and hosted by University of Oxford iGEM team agt 12th-13th July 2018. It was an amazing experience to talk with other people from the same field about our project getting very valuable feedback. Moreover, it was one of the first experience to present our project as well. Useful workshops made us to stop for a bit and rethink some of the aspects about or project. We are still excited about it.

Scottish iGEM Meetup

Scottish iGEM Meetup was held at The University of St Andrews and hosted by St Andrews iGEM 2018 team at 3rd of July. Hence, all three schottish teams participated St Andrews, Edinburgh_OG and us. We firs presented our projects, had discussion about them and as well we had some useful presentations about Human Practises and genera;

Hosting Meetup with Newcastle team

If you have ever heard about the biggest world arts festival Fringe in Edinburgh, you probably know how crazy it gets.

Bits and pieces

Besides meetups, labwork, we also had talks and chats with many other iGEM teams.

Mike the Microbe

Picture

Contact EdiGEM18

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