Difference between revisions of "Part:BBa K238015:Design"
(→Design Notes) |
|||
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K238015 short</partinfo> | <partinfo>BBa_K238015 short</partinfo> | ||
Line 7: | Line 6: | ||
===Design Notes=== | ===Design Notes=== | ||
− | + | This part was actually put in a pBR322 vector. This is a vector which has a low copy number (around 15-20). This is needed to make the promoter work properly in E.Coli. The low copy number ensures a good ratio between the promoter and its repressor, which is naturally present in E.Coli. When a high copy number is used, the promoter is abundant which results in a constituitivly active promoter. | |
− | + | ||
− | + | ||
===Source=== | ===Source=== |
Latest revision as of 15:55, 7 October 2009
blue light promoter and GFP
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 757
Design Notes
This part was actually put in a pBR322 vector. This is a vector which has a low copy number (around 15-20). This is needed to make the promoter work properly in E.Coli. The low copy number ensures a good ratio between the promoter and its repressor, which is naturally present in E.Coli. When a high copy number is used, the promoter is abundant which results in a constituitivly active promoter.
Source
the promotor comes from the genome of E.coli MC4100