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Rinl expression in different tissues and localization at the NMS. (A) RT-PCR was performed from different mouse tissue samples. Actin was used as quality control. (B) qPCR from cDNAs generated from different tissue RNAs was performed. Spleen was set to 1. s.e.m. is shown. (C) Mouse muscle sections were stained with anti-Rinl antibodies and Alexa 594-conjugated α-BGT. Images were taken on a confocal microscope. Scale bar, 20 μm.
