Regulatory

Part:BBa_J100337:Experience

Designed by: Anthony Eckdahl   Group: Campbell M Lab   (2017-10-19)
Revision as of 13:37, 16 November 2017 by Aneckdahl (Talk | contribs)


Here is the figure for v2 of repClone AM, 2017.

RepCloneAMFigure 1.png

AMrepCloneFigure 2.png

Cell type used was JM109. Data is average red fluorescence of 3 identical samples of each clone. Cells were grown in LB + AMP media. When aTc was present, its concentration was 0.2 micrograms/mL. X1-3 were all believed to be J100337 (our designed promoter) in J100205 (repClone). Each was isolated based on perceived level of red fluorescence (X1 being the most fluorescent and X3 being the least). WT was R0040 (wild type tet promoter). Negative control was J100205 alone. Positive control was J04450 (a sequence known to have a strong promoter, RBS, and RFP). J100328 was also used as a control. Table shows the ratios for each clone of red fluorescence produced in the presence of aTc divided by re fluorescence produced in the absence of aTc


Applications of BBa_J100337

User Reviews

UNIQc205cc0e330016bf-partinfo-00000000-QINU UNIQc205cc0e330016bf-partinfo-00000001-QINU