IGEM:Paris Bettencourt 2012/Notebooks/modularity group: Difference between revisions
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=Projects= | =Projects= | ||
==PKU 2010== | ==PKU 2010 [http://2010.igem.org/Team:Peking]== | ||
===concept=== | ===concept=== | ||
===the circuit=== | ===the circuit=== | ||
===comment on the modularity=== | ===comment on the modularity=== | ||
==Cambridge 2010== | ==Cambridge 2010 [http://2010.igem.org/Team:Cambridge]== | ||
===concept=== | ===concept=== | ||
===the circuit=== | ===the circuit=== | ||
===comment on the modularity=== | ===comment on the modularity=== | ||
==Bristol 2010== | ==Bristol 2010 [http://2010.igem.org/Team:BCCS-Bristol]== | ||
===concept=== | ===concept=== | ||
===the circuit=== | ===the circuit=== | ||
===comment on the modularity=== | ===comment on the modularity=== | ||
==Hongkong 2011 | ==Hongkong 2011 [http://2011.igem.org/Team:Hong_Kong-CUHK]== | ||
===concept=== | ===concept=== | ||
===the circuit=== | ===the circuit=== |
Revision as of 02:31, 2 July 2012
Purpuse of this group
Projects
PKU 2010 [1]
concept
the circuit
comment on the modularity
Cambridge 2010 [2]
concept
the circuit
comment on the modularity
Bristol 2010 [3]
concept
the circuit
comment on the modularity
Hongkong 2011 [4]
concept
the circuit
comment on the modularity
What we are doing now
PKU 2010
communication, requests of plasmids. searching for mercury, it seems that we need 2 strains: BL21DE3 and DH5 alpha depending of the part of the project we want to do. (both?)
Cambridge 2010
We have the biobrick we want to use (but there are 2 in fact): 2012 Kit Plate 4 well 17M, resistance: C But should we go on with that project? it uses the pBad promoter.
Bristol 2010
We have the biobrick: complete system: 2012 Kit Plate 4 well 1A, resistance: C
finding nitrates?
Hongkong 2011
complete system: 2012 Kit Plate 5 well 21I --> transformation?