Difference between revisions of "Part:BBa P10101:Experience"

Revision as of 08:52, 5 October 2018

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Applications of BBa_P10101

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 RTBV 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 it increased fluorescence to 1000x negative control levels, and between 10-100x that of RTBV levels.

[1) The GUS staining with the upper row of leaves is 35S, and is much stronger than the lower leaves which are using the RTBV promoter instead.]

File:Https://static.igem.org/mediawiki/2018/1/19/T--Cardiff Wales--mCherryPromoterAssayQuantified.png

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.

User Reviews

UNIQ802d3d5901699833-partinfo-00000000-QINU UNIQ802d3d5901699833-partinfo-00000001-QINU

@@ Line 10: / Line 10: @@
-https://static.igem.org/mediawiki/parts/3/34/35S%2BRTBV_GUS_NosT_results.png
-[[File:https://static.igem.org/mediawiki/parts/3/34/35S%2BRTBV_GUS_NosT_results.png|700px|thumb|left|Figure 1) The GUS staining with the upper row of leaves is 35S, and is much stronger than the lower leaves which are using the RTBV promoter instead.]]
+[[https://static.igem.org/mediawiki/parts/3/34/35S%2BRTBV_GUS_NosT_results.png|700px|thumb|left|Figure 1) The GUS staining with the upper row of leaves is 35S, and is much stronger than the lower leaves which are using the RTBV promoter instead.]]