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<p align="center"><strong><img src="https://static.igem.org/mediawiki/2012/d/de/Tabla1..JPG" width="527" height="197" /></strong></p> | <p align="center"><strong><img src="https://static.igem.org/mediawiki/2012/d/de/Tabla1..JPG" width="527" height="197" /></strong></p> | ||
| - | <p>The following shows the | + | <p>The constructions that were made, were confirmed by double digestions. The following image shows the digestions that correspond to the insert weight. |
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<p align="center"><img src="https://static.igem.org/mediawiki/2012/4/4f/Figura1.JPG" width="270" height="250" /></p> | <p align="center"><img src="https://static.igem.org/mediawiki/2012/4/4f/Figura1.JPG" width="270" height="250" /></p> | ||
Latest revision as of 04:08, 27 September 2012
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 RESULT The characteristics of said biopartsare described in the following table:
The constructions that were made, were confirmed by double digestions. The following image shows the digestions that correspond to the insert weight.
Fig 2: fluorescence of the different promoters when the bacteria were exposed to UV light.
Fig 3: GFP expression vs. Time, we can appreciate that the J23107 promoter is the strongest of the selected, our reference promoter was J23101
Fig 4: Polymerases per second, we can appreciate that the J23107 promoter is the strongest of the selected, our reference promoter was J23101 . With the previous results of the characterization of the promoters there is concluded that the promoter J23107, is the strongest because it produces more PoPs”
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