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March
- Our team was formally founded.
- All student members learned the fundamental knowledge of molecular cloning and iGEM.
- All student members looked through the previous excellent projects and learned the basic notion of synthetic biology and iGEM.
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April
- We divided into three groups and started to brainstorm separately (and we reported each’s progress every weekend).
- Our team was formally accepted by iGEM.
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May
- Our formal project was confirmed.
- The pre-experiment plan was confirmed.
- The division of labor was confirmed.
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June
- All student members learned laboratory fundamental qualities and received molecular cloning operation training.
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- 2017 DNA Distribution Kit Plates were received.
- We transformed all the biobricks we needed.
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- BBa_K2310001 constructed.
- BBa_K2310002, BBa_K2310003 and BBa_K2310004 constructed.
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July
- BBa_K2310005 constructed
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- BBa_K2310101 constructed
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- BBa_K2310000 constructed
- BBa_K2310103 constructed
- The first try of freeze dried bacteria
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August
- BBa_K2310006 constructed
- BBa_K2310007 constructed
- BBa_K2310008 constructed
- BBa_K2310100 tested
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- BBa_K2310009 constructed
- BBa_K2310011 constructed
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- BBa_K2310105 constructed
- BBa_K2310106 constructed
- BBa_K2310102 and BBa_K2310108 constructed
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- BBa_K2310107 constructed
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September
- Micro-fluid chip tested
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- BBa_K2310012 constructed
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- PCR amplified LPP, INP-SA and iLOV gene fragment and obtained the plasmid
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- Freeze dried bacteria experiments to explore some experimental conditions
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October
- The first round of the characteristic experiment
- The luxAB chemiluminescence experiment to explore some experimental conditions
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- The second round of the characteristic experiment
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- Hardware tested
Xiamen University, Fujian, China
No. 422, Siming South Road, Xiamen, Fujian, P. R. China 361005