Fig. 1
From: The genotypic and phenotypic impact of hypoxia microenvironment on glioblastoma cell lines
Expression of miRNAs in GBMs by qRT-PCR. The GBM cell lines were cultured under normoxic (21% O2) conditions. qRT-PCR was run using the SYBR green platform. The relative fold change difference was calculated using 2-ΔΔCT method where RNU6 was used as the normalizer. The data was analysed using 1-way ANOVA with Dunnett’s as a post-test and drawn using Graph pad prism. Each value represents the mean ± SD of three independent runs and * indicates p < 0.05; compared to the astrocyte’s cells