Classically, satellite cells were identified based on a unique anatomical location: beneath the surrounding basal lamina and outside the myofiber plasma membrane. This anatomical location gives satellite cells a “wedged” appearance when viewd by electrictron microscropy. This technique also revealed other morphological characteristics of satellite cells: large nuclear-to-cytoplasmic ratio, few organelles, small nucleus, and condensed interphase chromatin. This morphology is in harmony with the notion that most satellite cells, in healthy unstressed muscles, are mitotically quiescent (in G0 phase) and transcriptionally inactive. In addition to electron microscopy, satellite cells can be identified by phase-contrast microscopy on single myofiber explants. Based on the same principle, the behaviors of satellite cells on single myofiber explants can be recorded by utilizing live cell imaging techniques. The identification of satellite cells by fluorescence microscopy relies on specific biomarkers
Among biomarkers are: .α7-intergin, CD34 and etc. For more biomarkers see Figure 1 in the publication described in the following link: