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• W2291636574 abstract "Freshly isolated myocytes lose their viability and functionality very early, from single hours to single days. So their viability is usually tested before the experiments or monitored continuously in periodic time intervals. But simple observations using viability kits (e. g. LIVE / DEAD Cell Imaging Kit, Life Technologies) for this purpose are not sufficient because of Calcein photobleaching and furthermore repeated testing is not possible. In this paper we tested advanced methods based on Calcium degradation and fluorescence lifetime measurement or cardiomyocyte shape properties calculations." @default.
• W2291636574 created "2016-06-24" @default.
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• W2291636574 date "2015-09-01" @default.
• W2291636574 modified "2023-09-27" @default.
• W2291636574 title "Method for adult cardiomyocyte long-term viability monitoring using confocal microscopy techniques" @default.
• W2291636574 cites W1587343486 @default.
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• W2291636574 doi "https://doi.org/10.1109/cic.2015.7411072" @default.
• W2291636574 hasPublicationYear "2015" @default.
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