Difference between revisions of "Team:Calgary/MedalRequirements"

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                     We have created a parts collection (BBa_K2605000 to BBa_K2605004 and BBa_K2605009) for use in targeted gene integration and maintenance in eukaryotic cells. Each part in this collection has been verified with restriction enzymes and sequence confirmed for validity.  
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Revision as of 21:34, 17 October 2018

Team:Calgary/Medal Requirements - 2018.igem.org

MEDAL REQUIREMENTS


BRONZE

Registration and Attendance

The team has registered for and will be attending the 2018 Giant Jamboree in Boston from October 24th-28th.

Competition Deliverables
  • Wiki (In Progress)
  • Poster (In Progress)
  • Presentation (In Progress)
  • Judging Form (In Progress)
Attributions

Check out our Attributions page for detailed information concerning the contributions of team members, mentors, and advisors.

Characterization / Contribution

Our InterLab page shows how our team participated in the InterLab study this year.

SILVER

Validated Part / Contribution

We have created a parts collection (BBa_K2605000 to BBa_K2605004 and BBa_K2605009) for use in targeted gene integration and maintenance in eukaryotic cells. Each part in this collection has been verified with restriction enzymes and sequence confirmed for validity.

Collaboration

In addition to hosting the 2018 aGEM meetup, we worked with the NDC-HighRiverAB iGEM team, Queens Canada iGEM team, and the Lethbridge iGEM team on collaborations. See our Collaborations page for more details.

Human Practices

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GOLD

Integrated Human Practices

The integration of expert feedback played a major role in informing a pivot from gene therapy towards a research-oriented gene integration platform. Discourse involving bio-ethicists, researchers, university faculty, and spiritual thought leaders all contributed to the re-working of our initial plans to create a project that better suits the community's needs.

Improve a Previous Part / Project

Part BBa_K747096 was improved by the addition of a SalI restriction site upstream of the promotor. This new part, BBa_K2605001, is built to be compatible with our Multiple Cloning Site.