thank you for your kind response, i am agree with it , but if i have the sequence with me and i can design primer for it and will go for cDNA synthesis through random hexamer and go for amplification as for normal real time PCR. will it not work in this case?
i have this article with me and i trying my best to do it , but i dont think anything looks illogical in above-mentioned approach. but i am worried about secondary structures present in case of miRNA for this amplification purpose. i think peoples doing such thing will be more helpful but unfortunately i am not in contact with any of them.