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A proteomic profiling dataset of recombinant Chinese hamster ovary cells showing enhanced cellular growth following miR-378 depletion

机译:重组中国仓鼠卵巢细胞的蛋白质组分析数据集显示miR-378耗竭后细胞生长增强

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摘要

The proteomic data presented in this article provide supporting information to the related research article "Depletion of endogenous miRNA-378-3p increases peak cell density of CHO DP12 cells and is correlated with elevated levels of Ubiquitin Carboxyl-Terminal Hydrolase 14" (Costello et al., in press) [1]. Control and microRNA-378 depleted CHO DP12 cells were profiled using label-free quantitative proteomic profiling. CHO DP12 cells were collected on day 4 and 8 of batch culture, subcellular proteomic enrichment was performed, and subsequent fractions were analyzed by liquid chromatography tandem mass spectrometry (LC-MS/MS). Here we provide the complete proteomic dataset of proteins significantly differentially expressed by greater than 1.25-fold change in abundance between control and miR-378 depleted CHO DP12 cells, and the lists of all identified proteins for each condition.
机译:本文中提供的蛋白质组数据为相关研究文章“内源性miRNA-378-3p的消耗增加了CHO DP12细胞的峰值细胞密度,并与泛素羧基末端水解酶14的水平升高有关”(Costello等, 。,印刷中)[1]。使用无标记的定量蛋白质组学分析对对照和microRNA-378耗尽的CHO DP12细胞进行分析。在分批培养的第4天和第8天收集CHO DP12细胞,进行亚细胞蛋白质组富集,然后通过液相色谱串联质谱(LC-MS / MS)分析后续级分。在这里,我们提供了完整的蛋白质组学蛋白质组数据集,这些蛋白质组通过对照和miR-378耗尽的CHO DP12细胞之间的丰度变化大于1.25倍而明显差异表达,并提供了每种条件下所有已鉴定蛋白的列表。

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