Plasmids and Bacteria
From 2006.igem.org
(Difference between revisions)
Line 21: | Line 21: | ||
* Create RE biobrick (completed) | * Create RE biobrick (completed) | ||
- | *Isolating genomic DNA from Salmonella typhimurium | + | *Isolating genomic DNA from Salmonella typhimurium (completed) |
*Ordered oligos for recombinational enhancer and primers for the hin gene | *Ordered oligos for recombinational enhancer and primers for the hin gene | ||
+ | |||
+ | These sequences will be transformed into RFP and possibly GRP plasmids |
Revision as of 13:12, 7 June 2006
- pSB1A3
- amp resistant
- copy number:100-300
- size:2157 empty
- pSB1AC3
- part-BBAp1000
- copy number:100-3000
- amp and CmR resistant
- contains device that provides CmR
- size:3844 ( with device) 3005 (without device)
- pSB1AK3
- part BBa_|13535
- copy number:100-300
- amp and kan resistance
- contains a device for screening test
- size: 3457 (with device) 3189 (without device)
- Transform bacteria We are using Salmonella typhimurium for the Hin protein as it was the referenced species in all of the literature.
- Create RE biobrick (completed)
- Isolating genomic DNA from Salmonella typhimurium (completed)
- Ordered oligos for recombinational enhancer and primers for the hin gene
These sequences will be transformed into RFP and possibly GRP plasmids