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===
link: [http://2010.igem.org/Team:Cambridge]
===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===
link: [http://2010.igem.org/Team:BCCS-Bristol]
===the circuit===
===the circuit===
===comment on the modularity===
===comment on the modularity===


==Hongkong 2011==
==Hongkong 2011 [http://2011.igem.org/Team:Hong_Kong-CUHK]==
link: [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?

References