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. Author manuscript; available in PMC: 2007 Sep 21.
Published in final edited form as: Funct Integr Genomics. 2001 Sep;1(5):323–329. doi: 10.1007/s101420100037

Figure 3.

Figure 3

Semi-quantitative analysis of the expression of some genes coding for proteins detected by proteomics. RNA was extracted from monocytes and monocyte-derived DCs. RNA was reverse transcribed and cDNAs, corresponding to 7 ng, 20 ng and 100 ng (MnSOD, EFTu, ARP2–3 GP96, GBI-2), were amplified with gene specific oligonucleotides. PCR products were analyzed on 2% agarose gels. For each gene, the abundance ratio (DC/monocyte) was calculated by densitometry of the RT-PCR products.