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. 2015 Apr 1;25(2):78–84. doi: 10.1089/nat.2014.0517

FIG. 3.

FIG. 3.

Binding of fluorescent G4T4G4 PNA to 32P-labeled DNA hairpin and nonlabeled C4A4C4 DNA oligonucleotides. Two images of the same gel are shown: (A) 32P autoradiography and (B) fluorescent image. A fixed concentration (0.75 μM) of 32P-labeled DNA hairpin (left lanes on the gel), or nonlabeled C4A4C4 DNA (right lanes on the gel) were incubated with increasing concentrations (values on x-axis in C) of G4T4G4 PNA. Increasing amounts of fluorescently labeled G4T4G4 PNA were bound to the excess of C4A4C4 DNA oligonucleotide (B, right lanes). Fluorescence expressed in arbitrary units (au); PNA amount expressed in picomoles. Linear regression Y=91*X was used to calculate amounts of PNA in bands corresponding to PNA-hairpin complexes 1 and 2 (B, left lanes). Arrows 1 and 2 indicate the two shifted bands. (C) Calibration curve of the fluorescence of the bands in the gel versus amount of G4T4G4 PNA.