Difference between revisions of "Team:Glasgow/Collaborations"

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As a part of testing our bistable switch, we had to screen <i>E. coli</i> bacteria to detect fluorescence from GFP and RFP expression. Apart from the methods used in the lab, we also collaborated with the Cambridge iGEM team who designed the OpenScope microscope. (fig1) It is a 3D-printed brightfield and fluorescence imaging microscope that has the potential to be a low-cost tool accessible to anyone interested in microscopy. We therefore sent samples of bacteria expressing these proteins that they could use to test their microscope. As an outcome of this collaboration, we were also able to confirm some of our own results.
 
As a part of testing our bistable switch, we had to screen <i>E. coli</i> bacteria to detect fluorescence from GFP and RFP expression. Apart from the methods used in the lab, we also collaborated with the Cambridge iGEM team who designed the OpenScope microscope. (fig1) It is a 3D-printed brightfield and fluorescence imaging microscope that has the potential to be a low-cost tool accessible to anyone interested in microscopy. We therefore sent samples of bacteria expressing these proteins that they could use to test their microscope. As an outcome of this collaboration, we were also able to confirm some of our own results.
 
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<figcaption>Fig 1: The OpenScope microscope designed by the Cambrigde team as seen from the side.</figcaption>
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The samples we sent for imaging were:
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• DH5α –no plasmid, no antibiotic resistance, no fluorescence
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• DH5α - K1725103, Kanamycin resistance, GFP and RFP fluorescence
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• DH5α - K1725043 and K1725103, Kanamycin and Chloramphenicol resistance, RFP fluorescence
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• DH5α - K1725063 and K1725103, Kanamycin and Chloramphenicol resistance, GFP fluorescence
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• DH5α - K1725100 and K1725103, Kanamycin and Chloramphenicol resistance, GFP fluorescence with a few colonies expressing RFP
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Revision as of 00:26, 19 September 2015

Home > Collaborations

Cambridge Team
You got us under the microscope

As a part of testing our bistable switch, we had to screen E. coli bacteria to detect fluorescence from GFP and RFP expression. Apart from the methods used in the lab, we also collaborated with the Cambridge iGEM team who designed the OpenScope microscope. (fig1) It is a 3D-printed brightfield and fluorescence imaging microscope that has the potential to be a low-cost tool accessible to anyone interested in microscopy. We therefore sent samples of bacteria expressing these proteins that they could use to test their microscope. As an outcome of this collaboration, we were also able to confirm some of our own results.


Fig 1: The OpenScope microscope designed by the Cambrigde team as seen from the side.


The samples we sent for imaging were:
• DH5α –no plasmid, no antibiotic resistance, no fluorescence
• DH5α - K1725103, Kanamycin resistance, GFP and RFP fluorescence
• DH5α - K1725043 and K1725103, Kanamycin and Chloramphenicol resistance, RFP fluorescence
• DH5α - K1725063 and K1725103, Kanamycin and Chloramphenicol resistance, GFP fluorescence
• DH5α - K1725100 and K1725103, Kanamycin and Chloramphenicol resistance, GFP fluorescence with a few colonies expressing RFP

Location

Bower Building, Wilkins Teaching Laboratory
University of Glasgow
University Avenue
G12 8QQ

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