IGEM:IMPERIAL/2009
ToDo & Deadlines
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26 April 2024
11:38 | Hu:Publications diffhist +308 Hugangqing talk contribs |
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08:43 (cur | prev) +16,816 Xning098 talk contribs (Created page with "{{Template:CHEM-ENG590E}} ==Introduction== Microfluidics is the science and technology of systems that process or manipulate small (10 <sup> -18 </sup> to 10 <sup>−18 </sup> litres) amounts of fluids, using channels with dimensions of tens to hundreds of micrometres, as stated by George Whitesides. <sup> https://doi.org/10.1038/nature05058 1 </sup>. Microfluidic devices are microchemical systems such as labs on the chip, organs on the chip and plants on the chip....") |
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05:25 | Ernesto-Perez-Rueda:Contact diffhist −94 Ernesto Perez-Rueda talk contribs |
25 April 2024
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.
~ Tom Adie 15:44, 20 July 2009 (EDT)
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