Part:BBa_K562000:Experience
This experience page is provided so that any user may enter their experience using this part.
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how you used this part and how it worked out.
Applications of BBa_K562000
User Reviews
UNIQ5b7c871db468a21c-partinfo-00000000-QINU UNIQ5b7c871db468a21c-partinfo-00000001-QINU
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iGEM Dundee 2011 |
This part was seen work in practice. It is a published consitutive promoter, and we have shown it results in eventual protein production for numerous targets. See BBa_K562009 for the most detailed characterisation. |
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iGEM Dundee 2012 |
Although this part was seen work in practice, the Dundee 2012 team found that the rookie Dundee 2011 team had make some mistakes in their cloning. BBa_K562000 was found not to have been cloned to Biobrick [10] standard as the correct prefix and suffix sequences were not used. BBa_K562000 is now replaced by BBa_K895000. |
Results
A gene encoding an engineered mCherry protein was placed downstream of the tat promoter from BBa_K562000 and E. coli was transformed. mCherry fluorescence was observed by confocal microscopy as shown in Figure 1.
- Figure 1: Transcription and translation of mCherry driven by the E. coli tat promoter from BBa_K562000.
UNIQ5b7c871db468a21c-partinfo-0000000A-QINU