User:Cwoods
From 2006.igem.org
This is stuff I looked at and thought I should look at again, and stuff I wanted to look at while I was looking at other stuff so I didn't look at it yet, and stuff that maybe will help me learn more stuff, and stuff that maybe you should look at, and stuff that is interesting, cuz I don't put stuff here that is not interesting. Very helpful, I recommend making a stuff list if you have not already:
- Relate [http://partsregistry.org/Part:BBa_I15010 this] to [http://www.nature.com/nature/journal/v438/n7067/fig_tab/nature04405_F1.html this]
- Part [http://partsregistry.org/Part:BBa_M30109 M30109] (reason for different promoters?)
- Explore chromophore formation
- [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=books&doptcmdl=GenBookHL&term=promoter+AND+mboc4%5Bbook%5D+AND+372903%5Buid%5D&rid=mboc4.section.1269#1274 Genetic Switch Reference]
- [http://openwetware.org/wiki/BioBricks_construction_tutorial Biobrick construction]
- red light application
- strengthening promoters
- good reference?
- http://www.pnas.org/cgi/content/abstract/98/19/10566
- http://www.bgsu.edu/departments/chem/midden/pep/
- [http://www.bgsu.edu/departments/chem/midden/pep/transformed/photo001.html Pretty!]... aka What I looked at while I should have been doing other things.
- [http://mips.stanford.edu/public/abstracts/hastings.pdf bioluminescence.. more]
Note: The maximum light emission of a bacterial cell is about 104 q sec-1, meaning that to be seen, the cell density must be high, namely about 109 to 1010 cells ml-1.
- [http://partsregistry.org/Part:BBa_E0032 BBa_E0032] YFP (w/some mutation which could be unmutated back... i guess. Cuz I dont think we would want fast protein degradation and emission. Can be found in the wells of the 2006 plates. Could it be so easy? hmm... probably not. But I dont see any information to the contrary.)
