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In this study we used flow cytometry analysis of A-V/PI binding to study apoptosis and necrosis.
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TRITON can now be used to design ligand-binding proteins, to study protein ligand binding mechanisms or simply to dock any ligand to a protein.
Our study highlights the importance of integrating a systematic sequence and structure analysis of HA-glycan molecular interactions and a quantitative binding assay to study the effects of these interactions on the biochemical glycan receptor binding affinity of HA.
FTIR and SEM analysis of the biosorbents were performed to explore the type of functional groups available for metal binding and to study the surface morphology.
In this study, we describe the filter-trap method as an alternative to conventional dye binding assays to study amyloid fibril formation kinetics.
We used surface plasmon resonance (SPR) binding experiments to study the interactions between the LN LEa1 4 fragments of the α5, β1 and γ1 chains (Fig 3).
We developed the generalized tight-binding model to study the magneto-electronic properties of AAB-stacked trilayer graphene.
The mutations in the anti-CD20 variants were previously found not to affect FcRn binding in the soluble receptor-based assays; consequently, we used anti-Her2 variants with different binding affinities to FcRn to study FcRn binding assays.
Docking was performed on colchicine binding site of tubulin to study the binding mode of the designed compounds.
For a quantitative determination of binding affinities, it is important to study the binding to defined bile aggregates.
Molecular docking studies were performed on binding site of pantothenate synthetase protein to study the binding mode of compounds.
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