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Counting chambers

血细胞计数器

Company: VWR
Catalog#: 631-0975
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Single-molecule Analysis of DNA Replication Dynamics in Budding Yeast and Human Cells by DNA Combing
Author:
Date:
2017-06-05
[Abstract]  The DNA combing method allows the analysis of DNA replication at the level of individual DNA molecules stretched along silane-coated glass coverslips. Before DNA extraction, ongoing DNA synthesis is labeled with halogenated analogues of thymidine. Replication tracks are visualized by immunofluorescence using specific antibodies. Unlike biochemical and NGS-based methods, DNA combing provides unique information on cell-to-cell variations in DNA replication profiles, including initiation and elongation. Finally, this assay can be used to monitor the effect of DNA lesions on fork progression, arrest and restart. [摘要]  DNA梳理方法允许在沿着硅烷涂覆的玻璃盖玻片拉伸的单个DNA分子的水平上分析DNA复制。在DNA提取前,进行的DNA合成用胸苷的卤化类似物标记。使用特异性抗体通过免疫荧光可视化复制轨迹。与生物化学和基于NGS的方法不同,DNA梳理提供了DNA复制谱中细胞间细胞变化的独特信息,包括引发和延长。最后,该测定可用于监测DNA损伤对叉进展,停止和重新启动的影响。

背景 在称为复制起点的真核染色体上的数千个位点处启动DNA合成。原始激活遵循由检查点激酶和染色质的表观遗传修饰(Prioleau和MacAlpine,2016)控制的定义良好的复制计时程序。复制叉在正常S阶段经常停顿。叉停止是由多个事件引起的,例如DNA损伤,紧密结合的蛋白质复合物和高表达基因的转录(Tourriere和Pasero 2007; Zeman and Cimprich,2013)。真核生物已经制定了不同的策略来应对这种复制压力,包括修复机制来重新启动捕获的叉子和激活休眠复制起源以抢救终末抓捕的叉。
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Protoplast Preparation and Determination of Cell Death
Author:
Date:
2014-06-20
[Abstract]  The protoplasts assay constitutes a powerful tool that allows an easy uptake of active agents and a precise quantification of cell death induction in different populations. Our study showed that the basal level of cell death in our controls is low and stable throughout the length of our experiments (Danon et al., 2005; Pineau et al., 2013). In addition, the data obtained from the protoplast assay are applicable to intact seedlings, where it is possible to see differences in the intensity of necrotic lesions (Danon et al., 2006) even if those differences are not as easily and clearly quantifiable as with the protoplast assay. [摘要]  原生质体测定构成了一种强有力的工具,其允许活性剂的容易摄取和在不同群体中细胞死亡诱导的精确量化。 我们的研究表明,我们的对照中的细胞死亡的基础水平低并且在整个实验的长度上是稳定的(Danon等人,2005; Pineau等人, 2013)。 此外,从原生质体测定获得的数据适用于完整的幼苗,其中可以看到坏死损伤强度的差异(Danon等人,2006),即使这些差异不是 如同原生质体测定一样容易和清楚地定量。

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