RNA-seq analysis of control and MCUR1-depleted HSCs - BioProject
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE171094
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We sought to explore the underlying mechanisms by which MCUR1 promotes erythropoiesis. Total RNAs were extracted from cultured human CD34+ HPCs stably expressing sh-MCUR1 or sh-Ctrl under hypoxia (1% O2) following 2 days of EPO stimulation, using TRIZOL Reagent (Invitrogen, CA, USA). RNA sequencing (RNA-seq) was performed using Illumina NovaSeq6000 at Berry Genomics Co. Ltd. (Beijing, China), and a mean of 40 million paired-end reads per sample was obtained. mRNA profiles of NC and sh-MCUR1 CD34+ HPCs
创建时间：
2021-03-30
