Fig. 1.
Fig. 1. Virtual Northern blot analysis. / Total RNAs were extracted from cells in the peritoneal lavage fluid. cDNAs were synthesized and polyclonally amplified. Five hundred nanograms of PCR-amplified (nonsubtracted) cDNAs were electrophoresed on agarose gels (1.2%), and Southern blotted onto nylon membranes. These filters were hybridized at 65°C for 3 hours using Rapid-hyb buffer (Amersham Life Science) with [α-32P] dCTP-labeled cDNA probes. Filters were rinsed to a final stringency of 0.25 × SSC and exposed to a Kodak X-Omat or a Biomax film at −70°C with an intensifying screen. Probes used in this study were generated from the cDNA library made by RDA. GAPDH was used as a control of expression. Size markers on the left expressed in kilobase. GenBank accession nos. BE846999, BE8470001, and BE847000 for unknown #1, #2, and #3, respectively.

Virtual Northern blot analysis.

Total RNAs were extracted from cells in the peritoneal lavage fluid. cDNAs were synthesized and polyclonally amplified. Five hundred nanograms of PCR-amplified (nonsubtracted) cDNAs were electrophoresed on agarose gels (1.2%), and Southern blotted onto nylon membranes. These filters were hybridized at 65°C for 3 hours using Rapid-hyb buffer (Amersham Life Science) with [α-32P] dCTP-labeled cDNA probes. Filters were rinsed to a final stringency of 0.25 × SSC and exposed to a Kodak X-Omat or a Biomax film at −70°C with an intensifying screen. Probes used in this study were generated from the cDNA library made by RDA. GAPDH was used as a control of expression. Size markers on the left expressed in kilobase. GenBank accession nos. BE846999, BE8470001, and BE847000 for unknown #1, #2, and #3, respectively.

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