Regulatory

Part:BBa_K3783000:Experience

Designed by: Satvik Kethireddy   Group: iGEM21_OhioState   (2021-10-04)
Revision as of 02:34, 21 October 2021 by Satvik k (Talk | contribs) (→‎OhioState Application)


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Applications of BBa_K3783000

OhioState Application

The promoter was cloned into a luciferase reporter and then transformed into a strain of E.coli/i> expressing the fraR repressor. The luminescence curve for pFraB works as expected. There is a significant decrease, almost half, in expression in fraR- strains compared to fraR+ strains. This shows it is effective in controlling expression of expressed proteins. The fraR repressor was expressed via the lacZ promoter. This is why addition of IPTG results in increased repression.

pFraB Graph
Figure 1. pFraB Luciferase Reporter

User Reviews

UNIQ84a08611adc3a42b-partinfo-00000001-QINU UNIQ84a08611adc3a42b-partinfo-00000002-QINU