The Thermo Scientific Pierce Primary Cardiomyocyte Isolation Kit provides isolation and culturing reagents for the optimal yield and viability of primary cardiomyocytes from neonatal heart from mouse and rat.
The Primary Cardiomyocyte Isolation Kit has been designed to obtain high viability and purity of primary cardiomyocytes using validated reagents and an optimized procedure for enzymatic digestion and culturing. The kit contains two tissue-specific dissociation enzymes, media formulated for primary cell culture, and a cardiomyocyte cell culture growth supplement that promotes the isolation, enrichment and growth of functional cardiomyocytes. The validated protocol ensures optimal isolation and significantly reduces the processing time of isolation when compared to other methods. Addition of the cardiomyocyte growth supplement to culture cells further enriches for cardiomycytes, and cultures have been maintained for up to 7 days using the kit components.
Highlights:
Optimized - procedure and reagents optimized for viability, yield, purity, and ease-of-use
Time-saving - isolation protocol requires less than 2 hours compared to up to 21 hours by other methods
Yield - provides a 1.5- to 4-fold increase in yield compared to do-it-yourself methods and other commercial kits
Viability - provides higher viability than do-it-yourself methods and other commercial kits
Functional - cultured cardiomyocytes express the appropriate biochemical markers with validated beating activity
Includes:
Complete kit includes Cardiomyocyte Isolation Enzyme 1, Cardiomyocyte Isolation Enzyme 2, Hanks' Balanced Salt Solution (HBSS), DMEM for Primary Cell Isolation, and Cardiomyocyte Growth Supplement
Applications:
Cardiomyocyte cell differentiation
Immunohistochemistry (IHC)
Functional and biochemical assays
Biologically relevant system for preclinical drug discovery and predictive disease modeling
Product Details: Current methods for dissociation of cardiac cells from heart tissue require repeated (5 to 8 incubations) or lengthy (>16 hours) enzyme digestion, resulting in reduced yield and viability of isolated cells. The Pierce Primary Cardiomyocyte Isolation Kit provides fully optimized reagents and a protocol that prevents overdigestion for the isolation and culture of cardiomyocytes. The complete process from handling primary tissues to seeding cells in culture vessels can be completed within 2 hours. Because it uses optimized tissue-specific dissociation enzymes, this kit isolates cardiomyocytes with greater yield and cell viability than cells isolated by existing methods. The isolated primary cardiomyocytes express cardiomyocyte protein markers and exhibit contractile function, thereby providing a model system for studies of contraction, ischaemia, hypoxia and the toxicity of various compounds. References: 1. Louch, W.E., (2011) Methods in cardiomyocyte isolation, culture, and Gene Transfer. J Mol Cell Cardiol. 51(3):288-98. 2. Chlopcikova, S., et al. (2001) Neonatal rat cardiomyocytes – a model for the study of morphological, biochemical and electrophysiological characteristics of the heart. Biomed. Papers 145(2):49-55. 3. Gorelik, J., et al. (2004) Comparison of arrhytmogenic effects of tauro- and glycoconjugates of cholic acid in an in vitro study of rat cardiomyocytes. Int. J. Obstet. Gynaecol., 111:867-70.
