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SparkMind provides manual patch clamp electrophysiology services using primary cardiomyocytes isolated from rodent heart tissue, supporting detailed investigation of cardiac electrical activity and ion channel function.
This service is positioned to support mechanistic electrophysiology studies where high-resolution, cell-level electrical recordings are required. Primary cardiomyocytes preserve native ion channel composition and intrinsic electrophysiological properties, enabling precise evaluation of how compounds, genetic modifications, or experimental interventions affect cardiac excitability.
Primary cardiomyocytes isolated from rodent hearts provide a well-established experimental system for studying cardiac electrophysiology. These cells maintain native expression of cardiac ion channels and exhibit physiologically relevant action potentials suitable for detailed functional analysis.
The use of primary cardiomyocytes enables direct interrogation of cardiac electrical mechanisms under controlled in vitro conditions, supporting hypothesis-driven research and targeted electrophysiological validation.
Manual patch clamp remains the gold standard for high-fidelity measurement of cardiomyocyte electrical activity. In both voltage-clamp and current-clamp configurations, this technique allows direct recording of ionic currents and action potentials from individual cells.
This approach is particularly suitable for resolving subtle changes in current kinetics, membrane excitability, and action potential morphology that may not be detectable using indirect or higher-throughput methods.
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