Difference between revisions of "Part:BBa R0061:Experience"
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<I>iGEM Tokyo_Tech 2010</I><br> | <I>iGEM Tokyo_Tech 2010</I><br> | ||
Revision as of 21:30, 27 October 2010
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_R0061
User Reviews
UNIQa6d8a0edc3515334-partinfo-00000000-QINU
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iGEM Tokyo_Tech 2010
iGEM Tokyo_Tech 2010
In order to characterize R0061, Plux repression promoter, we constructed K395101 combining R0061 and K121013, which is a promoter-less gfp reporter (rbs-gfp-ter-ter) on pSB6A1 and used a fusion of PlacIq (I14032) to gfp (K121013) as a positive control and used promoterless gfp (K121013) as a negative control.
Overnight cultures of reporter strains grown at 37 °C containing appropriated antibiotics were diluted at least 1:100 and incubated at 37 °C as fresh cultures. After their OD590 reached 0.6, added 3OC6HSL. After 3 hours of induction, fluorescence intensity was measured with flow cytometry.
After 3 hours of induction by 3OC6HSL, the expression of GFP with 3OC6HSL dropped to 1/3 comparing with the expression without 3OC6HSL.
We confirmed that this promoter works correctly.
(→[http://2010.igem.org/Team:Tokyo_Tech/Project/Artificial_Cooperation_System/lux_act_rep more information])
UNIQa6d8a0edc3515334-partinfo-00000002-QINU
iGEM Chiba 2010
we also cheracterized about R0061.