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Assessing mitochondrial potential, calcium, and redox state in isolated mammalian cells using confocal microscopy.

Davidson, SM; Yellon, D; Duchen, MR; (2007) Assessing mitochondrial potential, calcium, and redox state in isolated mammalian cells using confocal microscopy. Methods Mol Biol , 372 421 - 430. 10.1007/978-1-59745-365-3_30.

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Abstract

Mitochondria play a vital role in the regulation of intracellular calcium dynamics. Fluorescent dyes can be used to provide a direct measurement of the redox state, mitochondrial membrane potential, and mitochondrial calcium content. The simplicity of this approach lends itself to high-throughput assays and time-resolved analyses; however, care must be taken to avoid artifactual results. We outline general methods using confocal microscopy for analysis of the redox state, mitochondrial membrane potential, and mitochondrial calcium content in adult cardiomyocytes. We demonstrate how these parameters can be analyzed in parallel using the emission spectra "fingerprinting" method even when emission spectra overlap.

Type:Article
Title:Assessing mitochondrial potential, calcium, and redox state in isolated mammalian cells using confocal microscopy.
Location:United States
DOI:10.1007/978-1-59745-365-3_30
Language:English
Keywords:Animals, Calcium, Cell Separation, Fluorescence, Membrane Potential, Mitochondrial, Microscopy, Confocal, Myocytes, Cardiac, Oxidation-Reduction, Rats, Rhodamines
UCL classification:UCL > School of Life and Medical Sciences > Faculty of Life Sciences > Biosciences (Division of) > Cell and Developmental Biology
UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Cardiovascular Science

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