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As select ECM components are known to regulate specific stem-cell functions, a robust characterization of cell-derived ECM proteomic composition is critical to better comprehend the role of the ECM in directing cellular processes.

Here, we characterized and compared the protein composition of ECM produced in vitro bkology bone marrow-derived MSC, adipose-derived MSC and neonatal fibroblasts dating matrix biology names from different donors, employing quantitative proteomic methods.

Each cell-derived ECM displayed a specific and unique matrisome signature, yet they all shared a common set of proteins. Check this out evaluated the biological response of cells cultured on the dating matrix biology names matrices and compared them to cells on standard TCPS.

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