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This was confirmed by zeta potential analysis of the Au NP solution with a mean Z-pot of −24.5 ± 3.1 mV, suggesting a stable gold colloid solution.
A surface charge potential analysis of the L1 motif reveals a linear basic patch on one face of the motif (Figure 2C).
Surface potential analysis of the entire (HhH 2 domain of SsoRadA protein revealed a 92° arched basic patch along the border of the second HhH motif (Figure 3D).
Surface potential analysis of the theoretical structure showed that these lysine residues form a cluster of positive charges interspersed with the hydrophobic residues (Fig 3A C).
Dynamic light scattering and zeta potential analysis of the nanoparticle reveals a size diameter of 88±2 nm and zeta potential of −54.5 mV.
Surface electrostatic potential analysis of the interaction interface showed that the majority of interactions between Fab 1F4 and E protein on DENV are likely to be between polar residues forming hydrogen bonds or salt bridges (Fig 5A and B).
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The streaming current was measured for a zeta-potential analysis of the flat-sheet membranes.
The homogeneity and stability of the treatment were assessed by a repeated zeta-potential analysis of the same and different membrane samples.
An example of this is the potential analysis of photosynthetic pathways between different samples (e.g., samples from upper and deeper levels of the ocean).
Test results of the zeta potential analysis of samples are provided in Table 3.
The UPLC-QTOFMS based metabolomics approach has great potential for analysis of the alterations of secondary metabolites of Angelica sinensis during growth.
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