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96 well culture plate

Company: Cellstar
Catalog#: 655180
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Measurement of Oxygen Consumption Rate (OCR) and Extracellular Acidification Rate (ECAR) in Culture Cells for Assessment of the Energy Metabolism
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Date:
2018-05-20
[Abstract]  Mammalian cells generate ATP by mitochondrial (oxidative phosphorylation) and non-mitochondrial (glycolysis) metabolism. Cancer cells are known to reprogram their metabolism using different strategies to meet energetic and anabolic needs (Koppenol et al., 2011; Zheng, 2012). Additionally, each cancer tissue has its own individual metabolic features. Mitochondria not only play a key role in energy metabolism but also in cell cycle regulation of cells. Therefore, mitochondria have emerged as a potential target for anticancer therapy since they are structurally and functionally different from their non-cancerous counterparts (D'Souza et al., 2011). We detail a protocol for measurement of oxygen consumption rate (OCR) and extracellular acidification rate (ECAR) measurements ... [摘要]  哺乳动物细胞通过线粒体(氧化磷酸化)和非线粒体(糖酵解)代谢产生ATP。已知癌细胞使用不同的策略重新编程它们的代谢以满足能量和合成代谢需要(Koppenol等人,2011; Zheng,2012)。此外,每个癌症组织都有其自己的个体代谢特征。线粒体不仅在能量代谢中起关键作用,而且在细胞的细胞周期调控中也起关键作用。因此,线粒体作为抗癌治疗的潜在靶标已经出现,因为它们在结构和功能上与其非癌对应物不同(D'Souza等人,2011)。我们详细介绍了利用海马XF24细胞外通量分析仪(图1)测量活细胞中氧耗率(OCR)和细胞外酸化率(ECAR)测量的方案。 Seahorse XF24细胞外通量分析仪持续测量细胞上清液中的氧浓度和质子流量(Wu等人,2007)。这些测量结果在OCR和ECAR值中转换,并能够直接定量线粒体呼吸和糖酵解。有了这个协议,我们试图评估三种不同癌细胞系的基线粒体功能和线粒体应激反应细胞毒性测试先导化合物甲磺卡西林,以研究其作用机制。将细胞铺在XF24细胞培养板中并保持24小时。在分析之前,将培养基替换为无缓冲的DMEM pH7.4,然后使细胞在非代谢通量分析前使用Seahorse XF在非CO 2孵育器中平衡以允许精确测量Milli-pH单位改变。 ...

Infectious Subviral Particle-induced Hemolysis Assay for Mammalian Orthoreovirus
Author:
Date:
2018-01-20
[Abstract]  Mammalian orthoreovirus (reovirus) utilizes pore forming peptides to penetrate host cell membranes. This step is essential for delivering its genome containing core particle during viral entry. This protocol describes an in vitro assay for measuring reovirus-induced pore formation. [摘要]  哺乳动物正面病毒(呼肠孤病毒)外壳在病毒进入之前或过程中经历一系列构象变化。 这些转换对于跨宿主细胞膜递送含基因组的核心是必要的。 该协议描述了用于监测向膜渗透活性形式(即,ISVP *)的转变的体外试验。

【背景】呼肠孤病毒是无包膜的双链RNA病毒,其由两个同心蛋白质壳组成:内衣壳(核心)和外衣壳(Dryden等人,1993; Zhang等人, / ,2005; Dermody et al ,2013)。在附着之后,病毒颗粒被内吞(Borsa et al。,1979; Ehrlich et al。,2004; Maginnis et al。,2006; Maginnis和宿主组织蛋白酶蛋白酶降解σ3外壳蛋白(Chang和Zweerink,1971; Silverstein等人,1972; Borsa等人,et al。 1981; Sturzenbecker等人,1987; Dermody等人,1993; Baer和Dermody,1997; Ebert等人, 2002年)。这个过程产生一个亚稳中间体,称为感染性亚病毒颗粒(ISVP),其中细胞穿透蛋白μ1被暴露(Dryden等人,1993)。 ISVPs是通过用糜蛋白酶处理纯化的病毒体而在体外产生的(Joklik,1972; ...

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