Difference between revisions of "Part:BBa P10101:Experience"
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[[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.]]
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[[File: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.]]
  
  

Revision as of 08:58, 5 October 2018


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

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.



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.




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

UNIQ2e0041207d7307d4-partinfo-00000000-QINU UNIQ2e0041207d7307d4-partinfo-00000001-QINU