| Types | DnaRegion
|
| Roles | promoter
Regulatory
|
| Sequences | BBa_M50023_sequence (Version 1)
|
Description
The vector will be expressed in an E. coli host. We've included the BCA1(FW) cut site and BCA1 (Rev) site on either side of our UV (360 nm) sensitive promoter. We want to use this promoter to drive the expression of GFP in the plasmid EColi_Promoter_Cassette.
Notes
We wanted to use a promoter that is compatible with E. Coli. In addition, we have flanked the promoter with BSA1 sequences that will allow the BSA enzyme to cut the promoter into another plasmic.
Source
We are using the same promoter as the iGEM Columbian Team 2007.
