Hi,
I have been culturing bovine digest satellite cells recently. In my very latest study, i seeded it at 2.65 million cell in T75 with dmem/f12+20% fbs and 1% antian and 10ng/mL fgf and tried proliferate the cell.
However, myotubes that were long and thin formed from satellite cells at 30% confluency, which should not have occurred.
Does anyone know what may be the cause for this to happen?