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Comparative analysis of mitosis-specific antibodies for bulk purification of mitotic populations by fluorescence-activated cell sorting

机译:荧光激活细胞分选用于有丝分裂种群大量纯化的有丝分裂特异性抗体的比较分析

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Mitosis entails complex chromatin changes that have garnered increasing interest from biologists who study genome structure and regulation fields that are being advanced by high-throughput sequencing (Seq) technologies. The application of these technologies to study the mitotic genome requires large numbers of highly pure mitotic cells, with minimal contamination from interphase cells, to ensure accurate measurement of phenomena specific to mitosis. Here, we optimized a fluorescence-activated cell sorting (FACS)-based method for isolating formaldehyde-fixed mitotic cells-at virtually 100% mitotic purity and in quantities sufficient for high-throughput genomic studies. We compared several commercially available antibodies that react with mitosis-specific epitopes over a range of concentrations and cell numbers, finding antibody MPM2 to be the most robust and cost-effective.
机译:有丝分裂需要复杂的染色质变化,生物学家对高通量测序(Seq)技术正在推动的基因组结构和调控领域的研究越来越感兴趣。这些技术在研究有丝分裂基因组中的应用需要大量高纯度的有丝分裂细胞,而间期细胞的污染极小,以确保准确测量特定于有丝分裂的现象。在这里,我们优化了一种基于荧光激活细胞分选(FACS)的方法,用于分离甲醛固定的有丝分裂细胞-几乎100%的有丝分裂纯度和足以进行高通量基因组研究的数量。我们比较了几种可在一定范围的浓度和细胞数下与有丝分裂特异性表位反应的市售抗体,发现抗体MPM2是最稳定和最具成本效益的。

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