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Enrichment of various exosome-associated lncRNAs with mass spec identified proteins – IP was carried out for the various mass spec identified proteins in triplicate with either (A) cells or (B) exosomes. The resultant elutes were subjected to qRT-PCR and enrichment of each lncRNA with the candidate protein relative to the IgG negative control following input standardization. The averages of triplicate IPs are shown.
