Total RNA was extracted from HepG2.2.15 cells with transfection of CPSF1 siRNAs or scramble siRNAs. Libraries were prepared using TruSeq Stranded mRNA kits (Illumina) and subjected to 150 cycle paired
Total RNA was extracted from HepG2.2.15 cells with transfection of CPSF1 siRNAs or scramble siRNAs. Libraries were prepared using TruSeq Stranded mRNA kits (Illumina) and subjected to 150 cycle paired
To further analyze the gene expression profile regulated by entecavir, we employed whole genome microarray expression profiling as a discovery platform to identify the differentially expressed genes.
