I am isolating total RNA from the roots of the eggplant plant for RNA-seq analysis. However, the density of the 18S band is higher than that of the 28S band. Has anyone encountered such a problem? Attached is the  figure of my RNA in 1% agarose gel (TAE buffer) stained with Redsafe. Could you comment on the quality and integrity of these RNA please? Thanks.

Similar questions and discussions