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− | <p><br><br>We collaborated with the <a href="https://2016.igem.org/Team:Gaston_Day">Gaston Day School</a> team this year to provide advice and analysis of their project. We maintained a line of communication and advised their team on how to proceed with Arabinose Induction to characterize certain part submissions. We | + | <p><br><br>We collaborated with the <a href="https://2016.igem.org/Team:Gaston_Day">Gaston Day School</a> team this year to provide advice and analysis of their project. We maintained a line of communication and advised their team on how to proceed with Arabinose Induction to characterize certain part submissions. We sent them a specialized E. coli strain for induction that has been use in our lab from North Carolina to them. We consulted our faculty mentor and engaged in thorough troubleshooting of their issues. We sent Parth Patel, a graduate of the Gaston Day iGEM team, to personally discuss plans, identify courses of action, and relay samples. We analyzed a colicin sample transformed in the pSB1C3 backbone through gel electrophoresis and sent back sequencing results to determine the status of their transformations. Following the competition we will continue to aid the team by doing transformations of colicin from original stocks into plates that contain antibiotic resistance so that the Gaston Day team's project may further progress.</p> |
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Revision as of 02:32, 20 October 2016
Collaboration with the Gaston Day School iGEM Team
We collaborated with the Gaston Day School team this year to provide advice and analysis of their project. We maintained a line of communication and advised their team on how to proceed with Arabinose Induction to characterize certain part submissions. We sent them a specialized E. coli strain for induction that has been use in our lab from North Carolina to them. We consulted our faculty mentor and engaged in thorough troubleshooting of their issues. We sent Parth Patel, a graduate of the Gaston Day iGEM team, to personally discuss plans, identify courses of action, and relay samples. We analyzed a colicin sample transformed in the pSB1C3 backbone through gel electrophoresis and sent back sequencing results to determine the status of their transformations. Following the competition we will continue to aid the team by doing transformations of colicin from original stocks into plates that contain antibiotic resistance so that the Gaston Day team's project may further progress.