Difference between revisions of "Part:BBa K2810002:Experience"
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− | [[File: | + | [[File:BBa_K2810002_OR_BBa_P10101_AND_K2810009_results.png|700px|thumb|center|Figure 2) |
The quantification report of the 35S promoter when linked to mCherry. This shows the raw photon output of leaf tissue in the table below it too, suggesting that the 35S CaMV promoter has expression 1000x that of the background level, and between 10-100x that of RTBV.]] | The quantification report of the 35S promoter when linked to mCherry. This shows the raw photon output of leaf tissue in the table below it too, suggesting that the 35S CaMV promoter has expression 1000x that of the background level, and between 10-100x that of RTBV.]] | ||
Revision as of 10:14, 5 October 2018
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Applications of BBa_K2810002
The Cardiff iGEM team of 2018 characterised this promoter using the GUS and mCherry reporter genes. We compared the expression of this promoter to that of the 35S CaMV promoter using the same reporter genes. These can be seen below. We found that using mCherry as a reporter gene, we could quantify the expression of the reporter, and found that the RTBV promoter increased expression levels to 10-100x that of background levels. This is still less than 35S CaMV promoter by a factor of 10-100.
We also performed an assay using eGFP to quantify this promoter. We used the RTBV promoter as it is supposed to have higher expression in vascular tissue, which Figure 3 shows. However, the raw quantification report did not show that it had significantly higher expression than control leaves, even though the values were higher.
User Reviews
UNIQ1121de271b7c38f9-partinfo-00000000-QINU UNIQ1121de271b7c38f9-partinfo-00000001-QINU