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Team:Chalmers-Gothenburg/Attributions
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The ideas from the Chalmers iGEM team were presented for the supervisors and advisors during a meeting. The supervisors and advisors only commented on the projects feasibility. The idea to develop a biodegradable pregnancy test kit was “thought out” by the students. | The ideas from the Chalmers iGEM team were presented for the supervisors and advisors during a meeting. The supervisors and advisors only commented on the projects feasibility. The idea to develop a biodegradable pregnancy test kit was “thought out” by the students. | ||
| - | The supervisors and advisors then helped the students to proceed with the project by illustrating the usefulness of the pheromone pathway. | + | The supervisors and advisors then helped the students to proceed with the project by illustrating the usefulness of the pheromone pathway. The supervisors also provided relevant articles. |
'''Homepage''' | '''Homepage''' | ||
Revision as of 12:40, 15 August 2012
Attributions
Idea
The ideas from the Chalmers iGEM team were presented for the supervisors and advisors during a meeting. The supervisors and advisors only commented on the projects feasibility. The idea to develop a biodegradable pregnancy test kit was “thought out” by the students. The supervisors and advisors then helped the students to proceed with the project by illustrating the usefulness of the pheromone pathway. The supervisors also provided relevant articles.
Homepage
All text, photos and graphics is written/taken/made by the students. The only exceptions are the sponsor logos and text that are directly provided by the sponsors.
Practical lab work and preparations
Most of the preparations for the laboratory work were done by the students such as plates, media and competent E.coli strains.
All laboratory work during the summer has been performed by the students. The students received some advice how to perform the experiments from supervisors and other staff in the System Biology group at Chalmers.
Materials
The LHCGR gene was ordered from a synthesizing company. The fmo gene was provided by Si Wouk Kim from Chosun University in South Korea and the tryptophanase gene was derived from genomic DNA from E.coli. The FIG1 promoter was amplified from genomic yeast DNA.
The final strain used (IMFD-73) was provided by the Kondo group from Kobe University in Japan and has the endogenous GPCR Ste2 and the feedback regulator Sst2 deleted. Five amino acids in the native yeast Gα protein are replaced by the corresponding ones from the human Gα protein.
The lab strain CEN.PK 113-11C and the plasmids pSP-GM1 and pIYC04 were received from the System Biology Group at Chalmers.
Modeling
Under construction.
