Expression profiling of wild-type, Prdm4 null and Prdm4-EGFP overexpressing mouse embryonic stem cells using Illumina whole genome V2 arrays. The hypothesis tested was that Prdm4 regulates gene expression consistant with Prdm4 genomic binding identified by ChIP-seq Prdm4 null embryonic stem cells were generated by gene targeting. Prdm4-EGFP overexpressing cells were generated through stable transfection. Total RNA was obtained from six wild-type ES cell clones, four Prdm4 null mutant ES cell clones and six Prdm4-EGFP overexpressing ES cell clones and hybridized to Illumina WG6_V2 arrays
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
电话: 0531-88819269