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Neonatal cardiomyocytes were isolated from P2 CD-1 ® hearts using the Neonatal Heart Dissociation Kit, mouse and rat, the Neonatal Cardiomyocyte Isolation Kit, mouse, an MS Column, and a MiniMACS ™ Separator. Subsequently, cells were fixed and stained using the Inside Stain Kit (# 130-090-477) and a FITC-conjugated antibody specific for cardiomyocytes (anti-α-actinin). Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Neonatal Cardiomyocyte Isolation Kit, ratFigure 1Neonatal cardiomyocytes were isolated from P2 CD-1 ® hearts using the Neonatal Heart Dissociation Kit, mouse and rat, the Neonatal Cardiomyocyte Isolation Kit, mouse, an MS Column, and a MiniMACS ™ Separator. Subsequently, cells were fixed and stained using the Inside Stain Kit (# 130-090-477) and a FITC-conjugated antibody specific for cardiomyocytes (anti-α-actinin). Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. | Neonatal Cardiomyocyte Isolation Kit, ratFigure 1Neonatal cardiomyocytes were isolated from P2 CD-1 ® hearts using the Neonatal Heart Dissociation Kit, mouse and rat, the Neonatal Cardiomyocyte Isolation Kit, mouse, an MS Column, and a MiniMACS ™ Separator. Subsequently, cells were fixed and stained using the Inside Stain Kit (# 130-090-477) and a FITC-conjugated antibody specific for cardiomyocytes (anti-α-actinin). Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Neonatal cardiomyocytes were isolated from P2 CD-1 ® hearts using the Neonatal Heart Dissociation Kit, mouse and rat, the Neonatal Cardiomyocyte Isolation Kit, mouse, an MS Column, and a MiniMACS ™ Separator. Subsequently, cells were fixed and stained using the Inside Stain Kit (# 130-090-477) and a FITC-conjugated antibody specific for cardiomyocytes (anti-α-actinin). Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Neonatal Cardiomyocyte Isolation Kit, ratFigure 1Neonatal cardiomyocytes were isolated from P2 CD-1 ® hearts using the Neonatal Heart Dissociation Kit, mouse and rat, the Neonatal Cardiomyocyte Isolation Kit, mouse, an MS Column, and a MiniMACS ™ Separator. Subsequently, cells were fixed and stained using the Inside Stain Kit (# 130-090-477) and a FITC-conjugated antibody specific for cardiomyocytes (anti-α-actinin). Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. | Neonatal Cardiomyocyte Isolation Kit, ratFigure 1Neonatal cardiomyocytes were isolated from P2 CD-1 ® hearts using the Neonatal Heart Dissociation Kit, mouse and rat, the Neonatal Cardiomyocyte Isolation Kit, mouse, an MS Column, and a MiniMACS ™ Separator. Subsequently, cells were fixed and stained using the Inside Stain Kit (# 130-090-477) and a FITC-conjugated antibody specific for cardiomyocytes (anti-α-actinin). Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
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