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This will determine the ideal concentration what amounts of Syk-TEVp for the best signal/noise ratio as well as characterize our circuit for use in other circuitsfor each placement of TCS-Gal4VP16 cause excessive constitutive production of reporter so we don't need to test those for the active test.  This will also characterize our circuits off behavior so we can compare it to its on behavior later to get the on/off ratio.  There is a test of no Gal4VP16 which will tell us how much constitutive eYFP our promoter produces.

BCR (CD79A+B (with and without TCS-Gal4VP16), IgM heavy, IgM light), Lyn, Syk-TEVp, tre-mKate(dox reporter circuit), UAS-eYFP(reporter circuit), hef1a:eBFP(transfection marker), (whatever is needed to make dox work).  We will be testing all combinations of CD79(A/B)-(stop/TCS-Gal4Vp16).

Dox, Beta Amyloid

All combinations of plasmids being tested will be prepared and put into dox ladders

First row is control for basal reporter expression.

The Expression We should identify what level of Syk-TEVp causes constitutive expression of the reporter should be much higher in Beta Amyloid than in the previous Beta amyloid- testand characterize the off behavior of our circuit so we will be able to compare it to the on behavior later. Our data will produce a scatter plot of eYFP (reporter) as a function of mKate (driven by the same promoter as syk).