Fig. 4.
Fig. 4. The effect of IFN-γ on the amount of cPLA2 protein. HL-60 cells were incubated with 2,000 U/mL of IFN-γ for indicated times and homogenized as described in Materials and Methods. Particulate and soluble fractions from HL-60 cells were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), transferred to nitrocellulose, and immunoblotted with rabbit antihuman cPLA2 antibody. A representative Western blot of membrane pellet (upper) and crude cytosol (lower) from HL-60 cells is shown. The cPLA2 protein was shown from left as follows: control cells (lane 1), cells treated with IFN-γ (2,000 U/mL) for 30 minutes (lane 2), 4 hours (lane 3), 12 hours (lane 4), 48 hours (lane 5), and 120 hours (lane 6). The size of the molecular marker is indicated on the left side.

The effect of IFN-γ on the amount of cPLA2 protein. HL-60 cells were incubated with 2,000 U/mL of IFN-γ for indicated times and homogenized as described in Materials and Methods. Particulate and soluble fractions from HL-60 cells were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), transferred to nitrocellulose, and immunoblotted with rabbit antihuman cPLA2 antibody. A representative Western blot of membrane pellet (upper) and crude cytosol (lower) from HL-60 cells is shown. The cPLA2 protein was shown from left as follows: control cells (lane 1), cells treated with IFN-γ (2,000 U/mL) for 30 minutes (lane 2), 4 hours (lane 3), 12 hours (lane 4), 48 hours (lane 5), and 120 hours (lane 6). The size of the molecular marker is indicated on the left side.

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