RNA isolation and Northern blot analysis were performed according to the procedure described previously [14]. Twelve micrograms of total RNAs from each sample was loaded in each lane. The probe was a 32P-labeled Glb1l4 cDNA fragment (from 2279 to 2615 bp in cDNA; total of 337 bp). An 18s r-RNA hybridization signal was used as a loading control. Autoradiographs with pronounced differences in expression were analyzed by densitometry.
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