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Effect of ETR-3 over-expression on endogenous CFTR exon 9 splicing. HeLa cells were transfected with the ETR-3 vector or the empty vector. After RNA extraction, RT–PCR was performed using a forward primer located in CFTR exon 8 and a reverse primer in CFTR exon 10. A control RT–PCR experiment was performed to assay the Caspase-2 exon 9 splicing event.
