Published: 25 September, 2017 | Volume 1 - Issue 1 | Pages: 075-091
Figure 1:
1S: Immunofluorescence analysis of the differentiation marker, myosin heavy chain, MyHC, in C2C12 cell line cultured in GM or DM. C2C12 cells were plated on glass slides for immunofluorescence and cultured for additional 120 hours in DM. After treatment, the cells were fixed, permeabilized and incubated with an antibody against the differentiation marker, myosin heavy chain, MyHC. Nuclei were stained with the chromomycin dye. The slides were analyzed by confocal fluorescence microscopy and significant images were acquired and displayed.
Read Full Article HTML DOI: 10.29328/journal.hjbm.1001007 Cite this Article Read Full Article PDF
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