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1 GT/-3', producing four base 3'-OH overhangs (sticky ends).
2 DNA template adjacent to the gene, leaving a sticky end.
3 ze on a nucleosome, generating two vacant CD sticky ends.
4 ell-structured branched DNA motifs tailed by sticky ends.
5 ity, was also constructed by the addition of sticky ends.
6 the intermolecular contacts are directed by 'sticky' ends.
7 sembly of cohesive single-stranded segments (sticky ends).5, 6 Methods that exploit the sequence addr
8 and of DNA composed entirely of concatenated sticky ends and that binds to four local neighbours duri
11 ends are flanked by a pair of dyes; when the sticky ends are disrupted, the dyes separate, and the fl
14 ate configurations, for example, homodimers, sticky-ended assemblies, and antiparallel arrangements.
18 bility and cooperativity of a network of DNA sticky-end associations could lead to greater control ov
21 on an edge adjacent to the binding site; the sticky ends can be disrupted if the protein binds with s
23 ination of synthetic stable branched DNA and sticky-ended cohesion has led to the development of stru
24 hnology combines branched DNA junctions with sticky-ended cohesion to create self-assembling macromol
28 e combination of branched DNA molecules and 'sticky' ends creates a powerful molecular assembly kit f
29 work, we demonstrate for the first time that sticky ended dimers are not a prerequisite for alpha-hel
30 f such nanofibers has been the formation of "sticky ended" dimers through careful selection of electr
34 irections of propagation associated with the sticky ends do not share the same plane, but extend to f
35 in charged pairs, and is inspired by similar sticky-ended fibrillation designs applied in DNA and coi
37 ion electron microscopy indicate that these "sticky-ended" fragments self-assemble via intermolecular
39 cifically designed arm lengths and intertile sticky-end interactions can be used to form sophisticate
40 ation with complementary single-stranded DNA sticky ends is increasingly used for guiding the self-as
42 e multiple cloning site via either blunt- or sticky-end ligation not only serves as a highly efficien
44 inside aquafoldamers can be created via the "sticky" end-mediated formation of 1D chiral helical stac
46 ive adsorption properties of the two 12-base sticky ends of the DNA molecules to partially immobilize
50 ary the number of linkers, the length of the sticky ends on the linker, and linker architecture and m
52 Functionalized with DNA with single-stranded sticky ends, patches on different particles can form hig
53 nd the generation of unique, non-palindromic sticky ends permits the formation of seamless junctions
54 the number and the relative position of DNA sticky-ends play a significant role in the stability of
55 r backbone, self-complementary "palindromic" sticky ends readily form intraparticle hairpins and loop
56 DNA target hybridizes this signal probe, the sticky end remains free to hybridize another target lead
59 modifications (1) confirms the importance of sticky-end stacking, (2) confirms the identity of the in
60 the solution an oligonucleotide duplex with 'sticky ends' that are complementary to the two grafted s
61 tural units are programmed by the design of 'sticky ends' that associate according to Watson-Crick co
65 ranched DNA molecules are linked together by sticky ends to produce objects, periodic arrays, and nan
66 , we find that the backbone that tethers the sticky ends to the surface can have a significant impact
68 methylene blue (a redox moiety) label and a "sticky end." When a DNA target hybridizes this signal pr
69 l are the free energies of ligation for each sticky end, which can be estimated by the calculator fro
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