Using small physical guiding templates, we demonstrated flexible control of aperiodic block copolymer DSA patterns with precise position and outstanding overlay accuracy.
In this paper, by grinding and pyrolyzing solid mixtures of an amino acid, an iron salt, and a mesoporous silica template, we demonstrate a solvent-free assembly approach to directly anchor both Fe3C nanoclucters and FeNx sites into nitrogen-doped ordered mesoporous graphitic carbon materials.
Using poliovirus polymerase and self-priming hairpin RNA substrates with 6- to 26-nt-long templating regions, we demonstrate that the assay can be used to determine Vmax rates for elongation and apparent Km values for nucleotide triphosphate (NTP) use.
Using a new DTI-based, density-weighted CST template approach, we demonstrated recently that CST injury measured in acute stroke patients with moderately-severe to severe motor impairment of the upper limb strongly predicts motor outcome of the limb at 6 months.
Further, we demonstrate template-stripped multilayer structures that have potential applications for photovoltaics and solar absorbers.
Starting from a framework of Co-based zeolitic imidazolate (ZIF-67) nanocubes, we demonstrate a template-engaged formation of double-shelled hollow structures with CoS-nanoparticle-assembled nanoboxes surrounded by outer CoS-nanosheet-constructed shells (denoted as CoS-NP/CoS-NS DSNBs).
In addition to the previously demonstrated applications of sequence alignment, fold identification, template selection, and homology modeling, we demonstrate herein, application of the described PCAIN-based structure prediction methodology to derive biological insight into potential structure-function relationships of proteins with hitherto unresolved structure.
As an example, we demonstrate roller template stripping of metallic nanoholes, nanodisks, wires, and pyramids onto the cylindrical surface of a glass rod lens.
In this study, we demonstrate that linear templates with short homology arms (∼30 60 bp) support robust integration of both small and large (gene size) edits in C. elegans.
We demonstrate that neither template backbone nor the architecture of the active site is perturbed by the oxoG anti)C and oxoGA pairs.
