IGEM:IMPERIAL/2009
ToDo & Deadlines
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Useful Links
- Encapsulation project
- Encapsulation Applications - Details
- Brainstorming
- Encapsulation applications brainstorming
- Ecoli wiki
- Feedback & Debriefs
- Specifications
Team Roles
Change your role when applicable
Charles - Cell Death
Dave - Cell Death/ Applications
Dineka - Encapsulation - biosynthetic pathway of alginate
James - Encapsulation - biosynthetic pathway of alginate
Kun - Encapsulation - biosynthetic pathway of alginate
Nuri - Cell Death
Royah - Compounds/BioBricks (Killing Strategy)/Timers (if time)/General
Tianyi - Compounds/Applications
Wiki Updates
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- This edit created a new page (also see list of new pages)
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16 April 2024
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10:20 | Yarn Microfluidics - Roger Dirth 12 changes history +442 [Rcostello (12×)] | |||
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08:18 | 3D Printed Microfluidic Robots - Helen Hua 2 changes history +6 [Michele Caggioni (2×)] | |||
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15 April 2024
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23:43 | User:Yanbin Huang 2 changes history +170 [Yanbin Huang (2×)] | |||
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22:11 | The paper that launched microfluidics - Xi Ning 14 changes history +9,705 [Xning098 (14×)] | |||
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21:45 | (Upload log) [Xning098 (4×)] | |||
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21:30 Xning098 talk contribs uploaded File:Figure 3 Set-up3.png | ||||
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21:24 Xning098 talk contribs uploaded File:Figure 2 Set-up1.png | ||||
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21:09 Xning098 talk contribs uploaded File:Figure 1 electroosmotic flow.png | ||||
Synthetic Biology @ Imperial
- Institute of Systems and Synthetic Biology
- Center of Synthetic Biology (press release)
- Synthetic Biology Course @ Imperial
iGEM resources
Advisor Contributions
Schumann lab from Uni. Beyreuth, DE have done some interesting work on using spores to direct antigens to the gut - to act as vaccines. Sporulation guys might also be interested in this paper, describing the B. sub coat protein (and how it's hilariously complex but not all required). Oh, and subtilis spores will germinate in the gut (probably), justifying using the killswitch!
Killswitch guys, I think perhaps looking into recombinases as opposed to restriction enzymes would be useful as they won't act on host DNA. Xer and Dif sites will recombine with themselves in presence of the required enzyme, excising any genes between them - you could flank genes with them, then express the enzyme to chop your construct up. Sites are required to be within ≈5kb of each other, I think, so random ones on host DNA shouldn't be affected. It might take a while to work so look into the time; could be useful as a fallback, anyway.
Biobrick images you can use if you need (advisors like named/labelled circuit diagrams!): 
~ Tom Adie 15:44, 20 July 2009 (EDT)
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