Fig. 3.
Fig. 3. Immunoblotting analysis of cyclin D1 and D3 protein abundance in total cell extracts of various exponentially proliferating human cells. Upper panel, cyclin D1 detection with the MoAb DCS-6; lower panel, cyclin D3 detected with the MoAb DCS-22. Cell types examined were PHA-stimulated normal lymphocytes (lane 1); WI38 diploid fibroblasts (positive control, lane 2); B-cell lymphoma lines harboring the t(11; 14) translocations JVM-2 (lane 3), K620 (lane 4), NCEB-1 (lane 5), and SP-49 (lane 6); MOLT-4 T-cell leukemia line (lane 7); and B-cell lymphoma lines lacking the t(11; 14) translocations Ramos (lane 8), Daudi (lane 9), and Namalwa (lane 10). Note the reciprocal expression of cyclins D1 and D3 among the lymphoma/leukemia-derived cell lines (lanes 3 to 6 versus lanes 7 to 10). The molecular weight of the markers is given in kilodaltons.

Immunoblotting analysis of cyclin D1 and D3 protein abundance in total cell extracts of various exponentially proliferating human cells. Upper panel, cyclin D1 detection with the MoAb DCS-6; lower panel, cyclin D3 detected with the MoAb DCS-22. Cell types examined were PHA-stimulated normal lymphocytes (lane 1); WI38 diploid fibroblasts (positive control, lane 2); B-cell lymphoma lines harboring the t(11; 14) translocations JVM-2 (lane 3), K620 (lane 4), NCEB-1 (lane 5), and SP-49 (lane 6); MOLT-4 T-cell leukemia line (lane 7); and B-cell lymphoma lines lacking the t(11; 14) translocations Ramos (lane 8), Daudi (lane 9), and Namalwa (lane 10). Note the reciprocal expression of cyclins D1 and D3 among the lymphoma/leukemia-derived cell lines (lanes 3 to 6 versus lanes 7 to 10). The molecular weight of the markers is given in kilodaltons.

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