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. 1999 Jul;10(7):2119–2129. doi: 10.1091/mbc.10.7.2119

Figure 3.

Figure 3

Determination of the amount of PCNA in the nuclear extract (GM1310B) used for the in vitro repair assays. Nuclear extract (75 μg) (lane 1) and different amounts of histidine-tagged PCNA protein (lane 2, 25 μg; lane 3, 50 μg; lane 4, 100 μg; lane 5, 200 μg) were electrophoresed on 4–12% SDS-PAGE and transferred to PVDF membrane per manufacturer instructions. PCNA was immunologically detected using an anti-human mouse monoclonal antibody to PCNA. The values for the standards were linear.