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- | Although this page is still in heavy construction, every guest is welcomed to left your trace on the "Doodle Board".
| + | '''Internationally Genetically Engineered Machine Competition''' |
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- | [[[['''Main Page''']]]] [Our Team]https://2008.igem.org/wiki/Team:Tsinghua/Our team
| + | Main Page Our Team Project Laboratory Work Parts Communication Doodle Board |
- | [ Project] [[Parts]]
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- | [[ Experiments]] [[Communication]] [[Links]] [[Doodle Board]]
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- | Our Team
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- | [[Image:Girls' Day 4.jpg]]
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- | ==Team Members ==
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- | Luying Jia [[Image:Luying Jia.jpg]] Yuanfan Yang
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- | Gechong Ruan Shan Lin
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- | Xin Rong Yicheng Long[[Image:Yicheng Long.jpg]]
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- | Ziying Liu Yuemeng Wang [[Image:Yuemeng Wang.jpg]]
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- | Yilong Zou [[Image:Yilong Zou.jpg]] Zi Wang[[Image:Zi Wang.jpg]]
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- | He Yang[[Image:He Yang.jpg]]
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- | Yongqiang Gou Chao Wang[[Image:Chao Wang.jpg]]
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- | Junjie Luo Cong Liu[[Image:Cong Liu.jpg]]
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- | Our Schedule
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- | Time Events
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- | Dec. 15, 2007 Team of Tsinghua University Founded
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- | Dec. 31, 2007 Brain Storm(1)
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- | Jan-Feb, 2008 Backgroud Investigation
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- | Feb.25, 2008 Brain Storm(2)
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- | Mar., 2008 Experimental procedure design;
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- | Modeling in silico Started
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- | Apr.1,2008 Wet Lab work started
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- | Apr.-Aug. ,2008 Wet Lab Work
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- | May.1, 2008 Team Registry
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- | May.25, 2008 Students’ Association of Synthetic Biology(SASB) Founded
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- | June.21, 2008 “Teach the teacher “workshop, in Kyoto, Japan
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- | Sept.-Oct., 2008 Inspection and Revision
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- | Oct.20,2008 Summary, Presentation Preparation
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- | Nov.8-9,2008 Jamboree In MIT,
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- | Project | + | |
- | This year we are trying to work at the motility of bacteria. E.coli senses some chemicals and moves toward
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- | or stays still, this behavior is called chemotaxis. Any modification of the pathway from the sensor to the
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- | motile apparatus will cause into different chemotactic effcts.
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- | Parts
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- | Communication
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- | Experiment and Protocol
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- | 1 PCR | + | |
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- | 1.1 Gold Faster Taq system:
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- | Reagent Concentration/Activity 50ul 100ul | + | |
- | GF taq buffer 10x 5 10 | + | |
- | GF taq 0.5 0.5
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- | dNTPmix 10mM each 1 2
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- | Primer 1 10uM 1 2
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- | Primer 2 10um 1 2
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- | Template DNA changeable 0.5 1
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- | MgCl2 0.2M 0.5 1
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- | ddH2O --- 40.5 81
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- | 1.2 The program under Gold faster taq system
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- | Progress Program I Program 2
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- | Predenaturing 95℃ 2-5 min 95℃ 2-5 min
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- | Denaturing 95℃ 10-20sec 95℃ 10-20sec
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- | Annealing (Tm-5) ℃ 2-5 sec 68℃ 10-15sec/1kb
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- | Extension 72℃ 10-15sec/1kb
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- | 25-30cycle 25-30cycle
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- | Last extension 1-2min or skipped 1-2min or skipped
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- | 2 Restriction cut:
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- | Reagent Concentration/Activity Volume(50ul system)
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- | Restriction cut buffer 10x 5ul
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- | Enzyme 1 -- 2.5ul
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- | Enzyme 2 -- 2.5ul
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- | Incubate at 37℃, 1.5 hrs or longer
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- | (Enzymes from Takara Co., Ltd)
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- | 3 Ligation:
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- | Reagent Volume(10ul system)
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- | Solution I 5ul
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- | DNA fragment 3.5ul
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- | Vector 1.5ul
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- | Incubate at 16-18℃,1hr or longer
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- | (Ligation kit from Takara)
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- | Links
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- | Tsinghua University:
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- | http://www.tsinghua.edu.cn/qhdwzy/index.jsp
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- | Parts:
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- | http://partsregistry.org
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- | Beijing Normal University:
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- | https://2008.igem.org/Team:Beijing_Normal
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- | ETH_Zurich:
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- | https://2008.igem.org/Team:ETH_Zurich
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- | Nature:
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- | http://www.nature.com
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- | Science:
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- | http://www.sciencemag.org
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- | System and Synthetic Biology:
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- | http://www.springer.com/biomed/journal/11693
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- | Doodle Board
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- | Oh, My E.coli, where are you! Yilong 08.7.11
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