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Fig. 5. Schematic of immunocytochemical staining of cultured mouse skeletal muscle. Top panels: location of myosin filaments (A-band), actin filaments (I-band), Z-line, A-band and I-band SR, and T-tubules. The overlay cartoon shows T-tubules and SR in a striated, well-differentiated myotube; this organization of T-tubules leads to the striated appearance of staining for DHPRs (Fig. 3G). In the inset the distribution of IP3Rs is shown in green, prominent in the terminal cisternae of the I-band SR. Such a distribution would give a double-banded cross-striated pattern (Fig. 4). Bottom panel: known immunocytochemical staining patterns of selected proteins. The relationship between IP3R staining (green) and known proteins in red: Ca2+ATPase (Fig. 2), {alpha}-actinin, myosin and {alpha}1 DHPR (Fig. 3). Colocalization of IP3R (green) and the red of Ca2+ATPase, {alpha}-actinin and {alpha}1 DHPR results in yellow.





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