To compare the clonogenic potential of primary BMSCs derived from BgnFmod KO and WT mice, bone marrow was flushed from femora and tibiae of 9-week old mice, plated in 25 cm2 flasks (106 cell/flask) with growth medium and left to grow untouched for 10d. Cells were then fixed with 100% methanol and following washes with PBS were stained with saturated methyl violet (Gibco) for 30 min. The number of colonies was obtained using light microscopy. Only colonies with more than 30 cells were counted.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.