Fig. 4.
Fig. 4. Detection of Sp1 and Sp3 in nuclear extracts from HeLa and PC3 cells by overlay with specific polyclonal antibodies of a Western blot analysis. / Proteins from HeLa and PC3 nuclear extracts were fractionated by sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE) (10% [wt/vol] for 2 hours at 150 V) and transferred to a PVDF membrane. The Western blot analysis was sequentially overlaid with specific polyclonal antibodies against Sp1, Sp3, and HMGB-1, and protein detection was performed by chemoluminescence. Sp1 as well as all 3 isoforms of Sp3 are present in HeLa and PC3 cell nuclear extracts in comparable amounts (Table 1).

Detection of Sp1 and Sp3 in nuclear extracts from HeLa and PC3 cells by overlay with specific polyclonal antibodies of a Western blot analysis.

Proteins from HeLa and PC3 nuclear extracts were fractionated by sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE) (10% [wt/vol] for 2 hours at 150 V) and transferred to a PVDF membrane. The Western blot analysis was sequentially overlaid with specific polyclonal antibodies against Sp1, Sp3, and HMGB-1, and protein detection was performed by chemoluminescence. Sp1 as well as all 3 isoforms of Sp3 are present in HeLa and PC3 cell nuclear extracts in comparable amounts (Table 1).

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