Fig. 4.
Expression of mOSMRβ mRNA. (A) Northern blot analyses of mOSMRβ mRNA in various cell lines. PolyA+ RNAs were prepared from various cell lines, and 1 μg of each sample was subjected to Northern blot analysis: lane 1, LO cells; lane 2, NIH3T3 cells; lane 3, Ba/F3 cells; lane 4, CCE cells; lane 5, M1 cells. (B) Northern blot analyses of mOSMRβ mRNA in various adult tissues; 1 μg of each sample was subjected to Northern blot analyses: lane 1, brain; lane 2, lung; lane 3, heart; lane 4, liver; lane 5, kidney; lane 6, small intestine; lane 7, muscle; lane 8, thymus; lane 9, spleen; lane 10, LO cells (upper panel). The middle panel shows the long exposure of the upper panel. The lower panel demonstrates equal loading by rehybridization with the GAPDH probe.

Expression of mOSMRβ mRNA. (A) Northern blot analyses of mOSMRβ mRNA in various cell lines. PolyA+ RNAs were prepared from various cell lines, and 1 μg of each sample was subjected to Northern blot analysis: lane 1, LO cells; lane 2, NIH3T3 cells; lane 3, Ba/F3 cells; lane 4, CCE cells; lane 5, M1 cells. (B) Northern blot analyses of mOSMRβ mRNA in various adult tissues; 1 μg of each sample was subjected to Northern blot analyses: lane 1, brain; lane 2, lung; lane 3, heart; lane 4, liver; lane 5, kidney; lane 6, small intestine; lane 7, muscle; lane 8, thymus; lane 9, spleen; lane 10, LO cells (upper panel). The middle panel shows the long exposure of the upper panel. The lower panel demonstrates equal loading by rehybridization with the GAPDH probe.

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