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Well, as you know, the stem-loop primer has a long chain, increasing the likelihood of undesirable secondary structure formation.
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Is there any difference between process time and temperature of cDNA synthesis using common primers (Oligo dT and Random Hexamer) compared with Stem-Loop primer of miRs?
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I have just 10^6 spores of Rhizopus in a sample. im using so fine glass pearls with Trizol and vortex about 10 min. but i cant see sharp bands of 28s,18s and 5s RNA in the agarose gel...
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