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Fig. 7 | Biomaterials Research

Fig. 7

From: A novel and cost-effective method for high-throughput 3D culturing and rhythmic assessment of hiPSC-derived cardiomyocytes using retroreflective Janus microparticles

Fig. 7

Quantification of of hiPSC 2D and 3D cardiomyocytes. (a) mRNA expression through real-time PCR analyses using primers for CM development markers (MYL7/TNNT2), gap junction/sarcomeric markers (CX43/DES), and the ion channel markers (CACNA1C/KCNJ3/SCN5A). Relative expression levels were normalized to those of GAPDH; (n = 3, *p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, and ****p ≤ 0.0001); (b) 2D and 3D culture of hiPSC-CMs assessed by flow cytometric analysis; (c) Western blot experiments demonstrating the difference of the above markers in 2D vs. 3D cultures of hiPSC-CMs

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