Hello,
I have got the purified recombinant enzyme and were eluted in 50mM sodium phosphate buffer and stored it in 15% glycerol at -20oC. The substrate for the enzyme is farnesyl pyrophosphate (FPP), which I have obtained from SIGMA and it came as farnesyl pyrophosphate ammonium salt (Methanol:ammonia::7:3). For how long will it be stable if diluted in phosphate buffer and how should I proceed further for analysis?