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Beilstein J. Nanotechnol. 2016, 7, 697–707, doi:10.3762/bjnano.7.62
Scheme 1: Schematic representation of creation of nanostructures from DNA–TPA hybrid self-assembly. The numbe...
Scheme 2: Synthesis of 2,6,14-triptycenetripropiolic acid.
Figure 1: 20% denaturing PAGE analysis of DNA (S1)–TPA conjugates showing a decrease in gel mobility of the c...
Figure 2: Native PAGE image (12%) of self-assembly of dicojugate DNA–TPA units with 2 μM total ssDNA concentr...
Figure 3: Native PAGE-gel image (8%) of self-assembled triconjugated DNA–TPA units with 2 μM total ssDNA conc...
Figure 4: AFM images of the self-assembly of DNA–TPA tri-conjugates. A and B in the presence of Zn PpIX and C...
Figure 5: Modeling studies involving S1–TPA and S2–TPA triconjugates showing a single tetrameric unit with sq...
Figure 6: The first-order-derivative melting curves of nanofibers (S1 DNA–TPA/S2 DNA–TPA triconjugate Zn PpIX...
Figure 7: CD spectra showing the chirality and conformation of nanofiber (S1 DNA–TPA/S2 DNA–TPA triconjugate ...
Figure 8: UV–vis absorption spectra and steady-state fluorescent spectra of rhodamine 123 quantifying the pho...
Beilstein J. Nanotechnol. 2015, 6, 1432–1438, doi:10.3762/bjnano.6.148
Scheme 1: Synthesis of ssDNA–melamine conjugates by a phosphoramidation reaction.
Figure 1: 30% denaturing PAGE analysis of the reaction mixture of ssDNA and melamine.
Figure 2: First-order derivatives of UV absorbance melting profiles at 260 nm for a control (R1–R2) and DNA–m...
Figure 3: 10% non-denaturing PAGE showing the difference in gel mobility of R1–R2 and the corresponding DNA–m...
Figure 4: (A) Linear assembly of di-branched conjugates (R1)2–melamine and (R2)2–melamine. (B) Network assemb...