Fig. 5.
Fig. 5. Western blot analysis of the cell-cycle–associated proteins Rb, p21 CIP1/WAF1, p27KIP1, CDK2, CDK4, cyclin D1, cyclin D2, cyclin D3, cyclin E, and p15INK4. / Total cellular proteins (15 μg/lane) were separated on 12.5% SDS-polyacrylamide gels and transformed to the membrane. For the analysis of Rb, 7.5% gels were used. Protein levels were detected by means of Western blotting with antibodies directed against each protein. pRb indicates hypophosphorylated Rb; ppRb, hyperphosphorylated Rb. Blots were stained with Coomassie brilliant blue to confirm that equal amounts of protein were present in each lane.

Western blot analysis of the cell-cycle–associated proteins Rb, p21 CIP1/WAF1, p27KIP1, CDK2, CDK4, cyclin D1, cyclin D2, cyclin D3, cyclin E, and p15INK4.

Total cellular proteins (15 μg/lane) were separated on 12.5% SDS-polyacrylamide gels and transformed to the membrane. For the analysis of Rb, 7.5% gels were used. Protein levels were detected by means of Western blotting with antibodies directed against each protein. pRb indicates hypophosphorylated Rb; ppRb, hyperphosphorylated Rb. Blots were stained with Coomassie brilliant blue to confirm that equal amounts of protein were present in each lane.

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