Hello everyone:

I am looking forward to analyze the differential composition of exosomal miRNA for a follow-up study. I would like to know which is the best approach for the normalization of the data obtained in the RT-qPCR:

- Should I add an spike-in control (cel-miR-39) during the extraction of the miRNA?

- Is it better to screen for stable exosomal miRNA in all my samples?

Thanks 

Jorge

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