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This will determine what amounts of Syk-TEVp for 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. |
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BCR (CD79A+B (with and without TCS-Gal4VP16), IgM heavy, IgM light), Lyn, Syk-TEVp, tre-mKaremKate(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
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All combinations of plasmids being tested will be prepared and put into dox ladders
First row is control for basal reporter expression.
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