Difference between revisions of "Team:Tianjin/Collaborations"

In our practice with people outside biology, we gradually found that production falls so far behind research that the public cannot understand its extraordinary meaning and scientists have difficulty in proving the value in their achievements. Hence, we initiated a joint research on how to apply a new technology to actual production.

In line with the principle of ‘To be more responsible and reflect more’, we jointly conducted a research on the transformation of biotechnology achievements with the iGEM team of Zhejiang University (ZJU-CHINA), the University of National Defense Science and Technology (NUDT_CHINA) and Ocean University of China (OUC_CHINA). Through the clear division of labor, we explored the general mode of the transformation in basic research results, and developed a series of HP activity guidelines and put them into practice by combining the features of iGEM competition and its own project features.

You can download the whole PDF HERE. For iGEMers to come, we sincerely hope it could offer you some help.

On September 16th, we are invited to Beijing-Tianjin iGEM Alliance Establishing Conference & Meet-up by UCAS-China. We presented our projects and discussed the current and future collaboration between member teams of this brand new Beijing-Tianjin iGEM Alliance. In addition, we communicated with teachers from the Institute of Biophysics. After, each team presented a small souvenir as the symbol of their team, put it into the collection case UCAS-China prepared for this conference.

We hope the league would promote communication and cooperation between us.

With the same interest in KaiABC oscillator, we kept close contact with XMU at the very beginning. Apart from communication in design and modeling, we had shared our plasmids that respectively carried RpaA, SasA and CikA with them as soon as we heard their problem.

We were glad to help them prepare the part backbone, pSB1C3 since they had too many biobricks to submit and the vector always run out.

They generously helped us measure the degradation of the origin with improved NanoLuc in 3 hours, proved our improved part could work effectively in Saccharomyces cerevisiae BY4741.