Additional file 9: of Clonal derivation of white and brown adipocyte progenitor cell lines from human pluripotent stem cells

Table S6. A non-targeted relative quantitative liquid chromatographyâ tandem mass spectrometry RP and HILIC)/MS/MS platform was used to capture 624 cell metabolites and 406 metabolites in their respective media at time of harvest. Data is shown for fBAT and NP88 in undifferentiated and differentiated (in serum-free medium containing rosiglitazone, T3, and ITS for 14â days) cells. Data for other progenitor and adult cell lines is also presented in this table. (XLSX 474 kb)

补充表S6。本研究采用非靶向相对定量液相色谱-串联质谱（结合反相RP和亲水相互作用HILIC两种分离模式）/MS/MS平台，在细胞收获节点捕获了624种细胞内代谢物及对应培养基中的406种胞外代谢物。数据涵盖未分化与分化状态下的fBAT及NP88细胞，其中分化诱导采用含罗格列酮（rosiglitazone）、三碘甲状腺原氨酸（T3）及胰岛素-转铁蛋白-硒（ITS）的无血清培养基，诱导时长为14天。本表同时收录了其他祖细胞系与成体细胞系的相关实验数据。（XLSX 474 KB）