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. 1999 Feb 22;144(4):789–801. doi: 10.1083/jcb.144.4.789

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Northern blot hybridization analysis of LYVE-1 receptor mRNA. RNA blots containing 2 μg poly(A)⁺ RNA per lane from each of the tissues shown were hybridized to a ³²P-labeled full-length LYVE-1 DNA probe (top), or glyceraldehyde-3-phosphate dehydrogenase probe (bottom), and washed at high stringency before autoradiography (see Materials and Methods). The migration positions of RNA calibration markers (kilodaltons) are shown to the left of the figure.