Hello, I wanted to do a reverse transcript for the subsequent realization of a sybr green qPCR. Classically I prepared my samples by mixing them with water, dNTPs, Random primers and the RNA of interest and finally at the time of denaturing them I realized that the thermocycler was out of order. My question is: can the samples be kept at -20 ° C until the thermocycler is operational, or do I have to start again for better RT? Thank you