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JC-1 Mitochondrial Membrane Po

tential Assay Kit
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  • 10009172-100 tests
  • 2025年07月11日
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    线粒体膜电位(ΔψM)是线粒体功能的重要参数,可作为细胞健康的指示物。JC-1是一种亲脂性阳离子染料,可以选择性进入线粒体,并随着膜电位的增加,反向改变颜色,从绿色变为红色。在具有高线粒体膜电位(ΔψM)的健康细胞中,JC-1自发地形成称为J-聚集体的复合物,显示出强烈的红色荧光。另一方面,在具有低膜电位(ΔψM)的凋亡或不健康细胞中,JC-1保持在单体形式,仅显示绿色荧光。Cayman的JC-1线粒体膜电位检测试剂盒提供所有必要的试剂及完整的操作说明,用于分析全细胞中的线粒体完整性。该检测试剂盒适用于荧光显微镜和荧光酶标仪。对于流式细胞术,推荐使用Cayman的JC-1线粒体膜电位流式细胞术检测试剂盒(Cayman_701560)。Mitochondrial membrane potential, (ΔψM), is an important parameter of mitochondrial function used as an indicator of cell health. JC-1 is a lipophilic, cationic dye that can selectively enter into mitochondria and reversibly change color from green to red as the membrane potential increases. In healthy cells with high mitochondrial (ΔψM), JC-1 spontaneously forms complexes known as J-aggregates with intense red fluorescence. On the other hand, in apoptotic or unhealthy cells with low (ΔψM), JC-1 remains in the monomeric form, which shows only green fluorescence. Cayman's JC-1 Mitochondrial Membrane Potential Assay Kit provides all the necessary reagents, as well as complete instructions, for analysis of mitochondrial integrity in whole cells. The assay is applicable to fluorescence microscopy and fluorescent plate reader. For flow cytometry, Cayman's JC-1 Mitochondrial Membrane Potential Flow Cytometry Assay Kit (Cayman_701560) is recommended.

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    相关实验
    • MitoProbe DiIC1 Mitochondrial Membrane Potential Protocol

      (V13241, prepared according to instructions accompanying that kit). 5)      Incubate the samples at 37°C for 15 minutes. (37°C is important to maintain membrane potential.) 6)      Add 400 μL annexin binding buffer. 7)      Analyze

    • Measurement of Mitochondrial Membrane Potential and Proton Leak

      The major component of mitochondrial electrochemical potential gradient of protons is the mitochondrial membrane potential (ΔΨ ), and hence it is a suitable parameter for assessment of mitochondrial function. Dissipation of the mitochondrial

    • Relation Between Mitochondrial Membrane Potential and ROS Formation

      to harmless H2 O. In this chapter, we describe a relation between mitochondrial membrane potential and the rate of ROS formation. We present different methods applicable for isolated mitochondria or intact cells. We also present experiments demonstrating

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