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Merck

Efficient Differentiation of TBX18

Stem cells and development (2016-12-09)
Jianmin Zhao, Henghua Cao, Luyang Tian, Weibang Huo, Kui Zhai, Pei Wang, Guangju Ji, Yue Ma
摘要

The epicardium promotes neovascularization and cardiomyocyte regeneration by generating vascular smooth muscle cells (SMCs) and producing regenerative factors after adult heart infarction. It is therefore a potential cell resource for repair of the injured heart. However, the epicardium also participates in fibrosis and scarring of the injured heart, complicating its use in regenerative medicine. In this study, we report coexpression of TBX18 and WT1 in the majority of epicardial cells during mouse embryonic epicardial development. Furthermore, we describe a convenient chemically defined, immunogen-free, small molecule-based method for generating TBX18

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Sigma-Aldrich
Triton X-100, for molecular biology
Sigma-Aldrich
IWR-1, ≥98% (HPLC)
Sigma-Aldrich
Triton X-100, laboratory grade
Sigma-Aldrich
IgG1 同种型对照 来源于鼠骨髓瘤, clone MOPC 21, purified immunoglobulin, buffered aqueous solution
Sigma-Aldrich
抗- 钙蛋白单克隆抗体 小鼠抗, clone hCP, ascites fluid