Fig. 4.
Fig. 4. PMA treatment upregulates the levels of p27Kip1 protein in U937 cells. (A) p27Kip1 Northern blot. Total RNA was isolated from U937 cells treated with PMA for the indicated times and 20 μg/lane was probed with a 32P-labeled p27Kip1 cDNA. The same gel was stained with ethidium bromide and photographed to show equal loading of RNA. (B) PMA upregulates the total cellular levels of p27Kip1 protein. Cell lysates (260 μg total protein) were resolved by SDS-PAGE and subjected to Western blotting with p27Kip1 antibody (1:5,000 dilution). (C) Cyclin E-associated p27Kip1 protein increases during PMA-induced differentiation of U937 cells. PMA-treated cell lysates (1.4 mg total protein) were immunoprecipitated with cyclin E monoclonal antibody agarose conjugate, and the associated proteins were subjected to Western blotting with a p27Kip1 antibody (1:5,000 dilution).

PMA treatment upregulates the levels of p27Kip1 protein in U937 cells. (A) p27Kip1 Northern blot. Total RNA was isolated from U937 cells treated with PMA for the indicated times and 20 μg/lane was probed with a 32P-labeled p27Kip1 cDNA. The same gel was stained with ethidium bromide and photographed to show equal loading of RNA. (B) PMA upregulates the total cellular levels of p27Kip1 protein. Cell lysates (260 μg total protein) were resolved by SDS-PAGE and subjected to Western blotting with p27Kip1 antibody (1:5,000 dilution). (C) Cyclin E-associated p27Kip1 protein increases during PMA-induced differentiation of U937 cells. PMA-treated cell lysates (1.4 mg total protein) were immunoprecipitated with cyclin E monoclonal antibody agarose conjugate, and the associated proteins were subjected to Western blotting with a p27Kip1 antibody (1:5,000 dilution).

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