I started using "RNA storage solution (1mM sodium citrate) from THermoFisher to dissolve RNA pellets and store in -20 or -80.

However, there is no amplification in the Q-PCR. it is frustrating and I am not sure if the solution affects the RNA, and if no do I have to change the RNA input?

I use 2 mcg RNA to make cDNA with high capacity superscriptII RT-kit (20 ul). but no luck so far in q-PCR?

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