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Timothy A. McCaffrey, Chenzhong Fu, Baoheng Du, Sukru Eksinar, K. Craig Kent, Harry Bush, Karl Kreiger, Todd Rosengart, Myron I. Cybulsky, Eric S. Silverman, Tucker Collins
Published in Volume 105, Issue 5
J Clin Invest. 2000; 105(5):653–662 doi:10.1172/JCI8592
Abstract | Full text | PDF
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Figure 2

Analysis of mRNA levels in human lesion by RT-PCR. (a) The mRNA was prepared from the dissected fibrous cap of the lesion (L) or the adjacent tunica media (M) within 5 minutes of surgical excision or after allowing an identical portion to incubate under transfer conditions for 65 minutes. The mRNAs were then analyzed by RT-PCR with primers directed at Egr-1 or RhoA. Two patients (E213, E217) are shown, demonstrating the difference noted in 3 of the 4 patients analyzed. (b) The difference in mRNA levels between media and lesion tissue was semiquantitated by serial dilution of the L mRNA before RT-PCR for Egr-1(upper band) or β-actin (lower band). Nonspecific amplification or contamination were not detected in water (H20) control.