04 August 2015 5 5K Report

I want to establish the high efficient cardiomyocyte differentiation system using mouse embryonic stem cell (mESCs). My colleague told me the hanging drop method (old and classical but famous one). This worked well a little bit but it was not enough efficiency (around 1-5%) to conduct further studies.

 I want to research the stress response of mESC-derived cardiomyocyte. It needs more purity and mass. If you know other better methods, please tell me.

 Now I'm planning to try the two following methods; glucose-depleted lactate-added culture (Shugo Tohyama, 2012) and Noggin treatment (Yuasa S, 2005).

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