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Whereas EVTs bound with great affinity to all α integrin subunits (Figure 6B), LacZ-expressing JEG-3 cells failed to bind to α1, α4, and αv antibodies (Figure 6B).
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Adsorption and displacement results agreed, indicating relatively high MW SRHA constituents bound with greatest affinity.
The result was (1) to give a daughter, SUMI-based composome (that bore some similarity to the mother composome) and (2) to release both unbound molecules (that were therefore unprotected and degraded) and a second daughter composome in which the molecules bound with greater affinity to one another than to the SUMIs.
However, this relationship does not always hold true; cis-permethrin and fenvalerate interact with both closed and open sodium channels, but they bind with greater affinity to the open state (Forshaw et al. 2000; Cantalamessa 1993).
The association of mouse Db heavy chain with monkey β2M is expected since mouse heavy chains bind with greater affinity to human β2M than to mouse β2M, conferring greater stability to the complex [26].
Unlike 17β-oestradiol, which displays relatively equivalent binding on both ER subtypes, and raloxifene, which binds with greater affinity to ER-α, genistein aglycone binds selectively to ER-β over ER-α, from 7- to 48-fold, depending on the assay system employed (Kuiper et al., 1997, 1998; Barkhem et al., 1998; Hsieh et al., 2006).
The drug binds with great affinity to the bacterial enzyme dihydrofolate reductase (DHFR) [21].
Introduction of the P2Shift mutations increased actin affinity whereas the P3Shift mutant bound with greater cooperativity than wildtype, but slightly reduced affinity (Figure 6A).
Dissociation constants obtained using both techniques revealed that some of the newly isolated chimeras bind 2F5 with greater affinity than previously identified chimeric rhinoviruses.
It has been less effective in transplantation models, but recent data from a nonhuman primate model [ 9] indicate that a mutated abatacept - namely belatacept, which binds CD86 with greater affinity - has promising effects.
Finally, the QSAR models were applied to the design of a peptide to bind with greater affinity than the known binding peptide sequences of the yRSP5-1 WW domain.
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Justyna Jupowicz-Kozak
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