I have extracted high integrity RNA and freeze-dried them for easier transport. What would be a proper method or protocol for reconstitution of the RNA. Is adding RNAse Free Water and vortexing enough?
Reconstitution with RNAse-free water and flipping should be absolutely fine, presuming that the RNA was previously solved in appropriate buffer (EDTA, pH 6-7).
Reconstitution with RNAse-free water and flipping should be absolutely fine, presuming that the RNA was previously solved in appropriate buffer (EDTA, pH 6-7).