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Statistical significance of the positive binding in comparison to the binding of the corresponding secondary antibody only was verified by ANOVA and is shown by asterisks.
Regarding the specific binding in comparison to others RTKs, the VEGFR-2 R-isomer had a 200-fold higher affinity versus epidermal growth factor receptor (EGFR) compare to only a 10-fold difference for S-isomer versus EGFR.
Our review of ninety-four polinies in total revealed several gaps, especially in relation to binding in comparison to nonbinding policies.
Our review of ninety-four policies across five key dimensions revealed several gaps, especially in relation to binding in comparison to voluntary policies.
Alternatively, the introduction of hydrophobicity could alter the association/dissociation constants for binding in comparison to the electrostatic interaction afforded by DISC1.
Residues R65, K72 and R73 were not observed by NMR to be responding essentially to CS4 binding in comparison to CS6.
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However, 11168-O grown at conditions mimicking mammalian and avian hosts had, in the majority of cases, significantly reduced Man-binding in comparison to 11168-GS grown under the same conditions.
This implies that target 5' XXXGGGXXX 3' binds to the same ZFP with higher binding affinity in comparison to the target 5' XXXGTAXXX 3' which binds with lower affinity to the same protein [ 30].
The cadmium-binding oyster proteins are minimally reactive in a competitive binding radioimmunoassay in comparison to the reactivity of a typical vertebrate metallothionein; the proteins may be metallothioneins, but, if so, they do not exhibit the principal determinants characteristic of vertebrate metallothioneins.
Patterns of pRBC binding to ICAM1 were similar to those seen for CD36, with homozygous α+thalassemia being associated with significantly lower pRBC binding (1891.9; 1320.5–2565.7) in comparison to normal pRBCs (2858.2; 2057.1–3790.8; P = 0.007) (Figs. 1, S3 & Table S1).
These interactions anchor 42 into the active site of CDK9 and may explain its high binding affinity in comparison to other compounds of the same series.
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