RNA-immunoprecipitation sequencing (RIP-seq) was performed to identify the transcripts under the regulation of DEAD-box helicase 3 X-linked (DDX3X). The BPH1-derived Cancer Progression (BCaP) cell lines were used for RIP-seq. Input and RIP RNA from the androgen receptor low/negative castration-resistant prostate cancer (ARL/- CRPC) BCaPMT10 and non-tumorigenic BCaPNT1 cells were extracted using the RNease Mini Kit. Libraries were prepared using the KAPA RNA HyperPrep Kit and sequenced on an Illumina HiSeq 2500 platform.
山东省济南市章丘区文博路2号
齐鲁师范学院 genelibs生信实验室
山东省济南市高新区舜华路750号
大学科技园北区F座4单元2楼
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