Difference between revisions of "Part:BBa K346016"
Line 3: | Line 3: | ||
This part was designed to characterize PmerT. When this plasmid was transformed to the bacteria expressing its correspondent activator MerR, the strain would be induced by Hg(II) to express GFP. The relationship between GFP intensity and the Hg(II)'s concentration helped us learn the character of PmerT. | This part was designed to characterize PmerT. When this plasmid was transformed to the bacteria expressing its correspondent activator MerR, the strain would be induced by Hg(II) to express GFP. The relationship between GFP intensity and the Hg(II)'s concentration helped us learn the character of PmerT. | ||
+ | |||
+ | [[Image:merT-E0840.jpg]] | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 15:38, 27 October 2010
PmerT(wt)(BBa_K346002)+lacZ(full length)(BBa_I732017)
This part was designed to characterize PmerT. When this plasmid was transformed to the bacteria expressing its correspondent activator MerR, the strain would be induced by Hg(II) to express GFP. The relationship between GFP intensity and the Hg(II)'s concentration helped us learn the character of PmerT.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]