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Sensing

PCR of the effector Backbones and the effector insert MMP2 and MMP9 without GFP
I did a 50ul PCR reaction of the Backbone and insert of the effector constructs. I again used a program where the first ten cylces are 10C° bellow the norma annealing temperature. The Gel electrophoresis showed that there was some sort of contamination, proably in the Primer Mixes. So I did the primer mixes again.

Nanoparticles

End of the ELISA-like assay: it worked!