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. Author manuscript; available in PMC: 2010 Feb 1.
Published in final edited form as: Free Radic Biol Med. 2008 Oct 18;46(3):352–359. doi: 10.1016/j.freeradbiomed.2008.09.038

FIGURE 2.

FIGURE 2

(A) PCR of treated and untreated with Fpg DNA fragments isolated from monomer, dimer, and trimer nucleosomal repeates and multi-nucleosomal zone with primers specific for the HRE of the VEGF promoter and 28S rRNA. (B) Pooled data for +/−Fpg PCR band intensity ratio. N = 6–8, *Different from normoxic controls at p<0.05.