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I am trying to study the preferential partitioning of an RNA containing long 3'UTR into stress granules (SG), as compared to an RNA isoform with shorter 3'UTR. A method that I found in Article Isolation of yeast and mammalian stress granule cores

detailed how to concentrate SG cores. Goal is to compare the mRNA levels of my 2 target RNAs (one with long 3'UTR and one with short 3'UTR) in these SG cores, by qPCR. It hasn't been fruitful. Has any one studied RNA composition/quantitation in stress granules using methods other than RNA-sequencing?
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