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Analysis of fibroblast growth factor receptor (Fgfr) expression in the mouse kidney. Aliquots (10 μg) of total RNA from mouse kidneys at E15.5 were resolved in parallel on an agarose gel, transferred to a nylon membrane and individually hybridized with radiolabeled probes for Fgfr1, Fgfr2, Fgfr3 and Fgfr4 as indicated. The migration positions of the ribosomal RNAs are indicated in the margin. As a loading control, the ethidium bromide stained 28S ribosomal RNA is shown.
