Fig. 5.
Fig. 5. Expression of messenger RNAs of murine G-CSF and IL-18Rα and IL-18Rβ in splenic adherent cells following stimulation with IL-18. / Splenic adherent cells (2 × 107 cells) were treated with IL-18 (100 ng/mL) for 6 hours, and messenger RNAs of G-CSF, IL-18Rα, IL-18Rβ, and GAPDH were analyzed by RT-PCR. Messenger RNA of lipopolysaccharide (LPS)-stimulated peritoneal macrophages was used as a positive (P) control. For negative control (N), the above mRNA was subjected to PCR reaction without prior RT reaction.

Expression of messenger RNAs of murine G-CSF and IL-18Rα and IL-18Rβ in splenic adherent cells following stimulation with IL-18.

Splenic adherent cells (2 × 107 cells) were treated with IL-18 (100 ng/mL) for 6 hours, and messenger RNAs of G-CSF, IL-18Rα, IL-18Rβ, and GAPDH were analyzed by RT-PCR. Messenger RNA of lipopolysaccharide (LPS)-stimulated peritoneal macrophages was used as a positive (P) control. For negative control (N), the above mRNA was subjected to PCR reaction without prior RT reaction.

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