CALENDAR
Human PracticesEducation
Meeting with Gem Mont Biotech Company
Bioman training(Education)
10/31Science Festival at National Museum of Natural Science
Bioman training(Education)
11/21Bioman training(Education)
Steam Fair
12/31Mingdao IGEM 2020 Presentation
Meeting with Professor Chih-Hsin Hung at I-Shou University
Phage-hunting
02/25Salmonella phage identification
02/27Phage amplification
Salmonella phage titration
03/12Cloning: TPase-HisN/pSB1C3
03/16Meeting with Professor Guo-Jen Wang at National Chung Hsing University
03/26Cloning: J04450/pSBII-SK-mTol2
Test T7-His-phi29 DNA polymerase fro team TAS_Taipei
04/12Cloning of ldhp-GFP-Tr/pBSII-SK-mTol2
Protein purification: His-phi29 DNA polymerase
04/27Meeting with Creative LifeSciences Company
Cloning: ldhp-KanR-Tr/pBSII-SK-mTol2
05/19TXTL: reagent preparation
Cloning : ldhp-Phi29-HisN/pBSII-SK-mTol2
Meeting with TAS IGEM 2021
06/04Cloning : ldhp-RFP, amilCP/pBSII-SK-mTol2
06/08Planning modelling version 1: attempt to model optimal waiting time during product usage through the mean of computer simulation of bacteria-phage interaction
06/11Found simulation program eVivaldi by researchers. Plan to renew and remake so that it is appropriate for reaching our goal.
06/12Meeting with KCIS IGEM 2021
06/15Start to design Ni-column
06/18Design of Ni-column complete. Ordering materials
06/23Renewal of eVivaldi complete, now runs on the newest version of Python. Start to add in new functions and remove unwanted functions, adjusting the program to our needs.
06/24Cloning : pSB6K1 & pSB6C1 (pBR322-based)
06/25TXTL: in vitro expression of His-TPase (Tol2 transposase)
06/30HisPurTM Ni-NTA Resin arrived
Cloning :ldhp-GFP-Tr/pSB6A1& pSB6K1 & pSB6C1
Cloning :Adjustment complete. However, testing shows that result is far from correct. The program’s algorithm also requires input of factors, such as characteristics of phages, that is difficult to measure in our lab
07/9First successful Ni-column produced
Formal meeting of the team deciding whether to change direction. Ultimately decided to get back to mathematical modeling instead of computer simulation. Start to search for theories and researches that will assist in modeling
07/10Protein purification: His-TPase
07/19Meeting with Micreos CSO – Steven Hagens
07/21Start to design the Luer-lock connector
Found core research paper that helps modeling optimal latent time
07/22In vitro plasmid integration assay(1)
07/23Meeting with NCKU IGEM 2021
07/25In vitro plasmid integration assay(2)
07/26Conduct experiment to collect data for future use in modeling
07/27In vitro plasmid integration assay(3)
07/30Rough design complete, 3D model design starts
Briefly organized the equation and logic of the model. Tested using the collected data, but result turned out to be counterintuitive.
08/04In vitro phage engineering
Meeting with Warwick IGEM 2021
08/063D model version 1 complete, test failed. Start to design version 2
08/143D model version 2 complete, adequate yet many small issues exist. Start to design version 3
08/19Found a research paper explaining the strange phenomenon. Consider the model as complete.
08/203D model version 3 complete. Passed the test with enough precision. However, the core mechanism breaks after a few tests.
08/21Scheduled consultation with 3D printing teacher in school
08/24Salmonell test
08/26Consultation with a 3D printing teacher in school. Decided to change to photo-curing 3D printing
3D model version 3 reprinted with photo-curing 3D printing
09/08Testing with Ni-column installed.
09/10Finished wiki modeling page content
09/15Filming demonstration video
09/20Content review complete
09/22Demonstration video finished
09/30Visiting FDS Taichung
Visiting He-Feng chicken farm