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Owing to its diversified structures, high affinity, and specificity for binding a wide range of non-nucleic acid targets, aptamer is a useful molecular recognition tool for the design of various biosensors.
After a short, general physico-chemical introduction to CNTs, we introduce different methods for CNT surface modification, facilitating their dispersions in physiological solutions, on the one hand, and binding a wide range of molecules or drug-loaded liposomes, on the other.
Our results demonstrate the high affinity that GO has for binding a wide range of aqueous metals, and the results can be used to estimate with a reasonable degree of certainty the distribution of metals in complex GO-bearing environmental or engineered systems.
Bet v 1 has a Y-shaped, solvent accessible hydrophobic cavity traversing the core of the molecule, capable of binding a wide range of ligands.
In contrast, batch B showed a CD spectrum typical for Bet v 1. Crystallization of several Bet v 1 isofoms revealed that the core of the protein is traversed by Y-shaped, solvent accessible, hydrophobic cavity capable of binding a wide range of ligands [24], [25], [26].
Aptamers are single-stranded oligonucleotides with a size of 15 60 nucleotides selectively binding a wide range of biomolecules, including whole cells.
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Such a function was of interest because the presence of 2Fe-2S ferredoxinsuggesteded that the β-GF domains could potentially provide a scaffold for binding a wider range of small molecules or other prosthetic groups.
Transferrin is capable of binding to a wide range of synergistic anions at its iron binding site, and formation of an iron arsenate transferrin complex is presumably responsible for arsenate transferrin binding.
Whereas CB2 binding did not vary greatly among all of the samples, the CB1 binding showed a wide range of affinities.
Antibodies and recombinant antibody binding domains are potentially useful agents to achieve cell-specific targeting, due to their unparalleled affinity and specificity of binding to a wide range of target cell surface markers.
PAR is the most electronegative biopolymer and this property is essential for its binding with a wide range of proteins.
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