Difference between revisions of "Part:BBa K3783001:Experience"

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===Applications of BBa_K3783001===
 
===Applications of BBa_K3783001===
  
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The promoter was cloned into a luciferase reporter plasmid and then transformed into a fraR expressing strain of <i>E.coli</i>. The repressor protein has been expressed under the lacZ promoter thus addition of IPTG results in increased amounts of repressor. The luminescence curve of the fusion promoter follows mostly as expected. There is a significant, almost threefold, repression of production of target proteins in the fraR+ strains. However, due to the presence of the pR, the proteins are produced at a massive scale, in the millions of light units.
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=OhioState Application=
 
=OhioState Application=
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<p> The promoter was cloned into a luciferase reporter plasmid and then transformed into a fraR expressing strain of <i>E.coli</i>. The repressor protein has been expressed under the lacZ promoter thus addition of IPTG results in increased amounts of repressor. The luminescence curve of the fusion promoter follows mostly as expected. There is a significant, almost threefold, repression of production of target proteins in the fraR+ strains. However, due to the presence of the pR, the proteins are produced at a massive scale, in the millions of light units.
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Revision as of 02:50, 21 October 2021


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_K3783001

OhioState Application

pR-pFraB Graph
Figure 1. pR-pFraB Luciferase Reporter

User Reviews

UNIQ8ca3814749608cef-partinfo-00000001-QINU UNIQ8ca3814749608cef-partinfo-00000002-QINU