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43, 65, 66 The majority of the substrate (FA) and the end product (acyl-CoA) of the enzymatic reaction do not exist free in the cytosol under physiological conditions, but are rather bound to FABPs 67 or ACBPs.
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Yet, carriers may rather bind to the extensive capillary bed where shear stress is minimal.
In addition, the agonistic anti-Fas CH-11 IgM antibody and anti-TRAIL receptor 2 IgG antibody Apomab recognise this region of the death receptors, whereas anti-DR5 BDF2 and our antibody anti-Fas E09 rather bind to CRD1 and CRD2.
Finally, this study presents the first identification of mercury and methylmercury biothiols in spiked plant extracts; hence, this method is a novel tool to investigate whether mercury and methylmercury indeed form complexes with biothiols such as Cys and GS, or if they rather bind to larger entities such as phytochelatins in plants or proteins in fish and other biota.
Indeed in some cases, it has been shown that a molecule of solvent would rather bind to the vacant site of the cation than [BF20]−; this is a testament to the anion's non-coordinating nature [133, 134, 135].
VM extracts being more of the noncompetitive type inhibitor implies that the bioactive components responsible for such action would rather bind to a region beside the active site which is a major advantage over acarbose which is a competitive inhibitor.
These electrons, though mobile within the metal, are rather tightly bound to it.
The calculated results show that Melamine molecules are rather strongly bound to the surface of both defect and defect free GNRs; it can also be found that Melamine molecules prefer to be adsorbed on Si-doped GNR.
Similarly, Orc2 started to be detected (∼3-fold enrichment) in early G1 and remained rather constantly bound to the origin.
In contrast, STxB is rather homogeneously bound to membranes containing Gb3 with a mono-unsaturated fatty acid (22∶113), which is less densely packed, and is not organized in macroscopic domains, from which perylene is excluded.
Some advantages are the following: (1) The MassCode system employs primers, probes, targets and codes that are all in homogeneous solution during target hybridization steps rather than bound to a surface or interacting with a solid/liquid interface as with suspension arrays and microarrays [30] [33].
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CEO of Professional Science Editing for Scientists @ prosciediting.com