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The N-terminus of both peptides was found to be in the solvent layer in both the DPPC/PG and PC/PG membranes.
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The effect of both peptides is found to be greater than the total activity calculated for the effect of each peptide, separately (Todorov 2009).
Although both peptides were found to be bactericidal against a variety of clinical isolates with different antibiotic resistance profiles, hep-20 was active at lower concentrations than hep-25, in most of the cases.
Both peptides were found in cell extracts from two different persons and none of the found modifications was previously known.
Both peptides are found in amyloid plaques that, according to the amyloid cascade hypothesis [2], [4], eventually lead to the neurodegeneration.
Both peptides were found to be active against P388 leukemia, S180 ascites and spontaneous ovarian tumor of mice upon intra-peritoneal injection of peptides, but with the all-D peptide showing significantly higher in vitro activity than the all-L peptide (Baker et al., 1993).
Peptide cyclization of the hexameric peptides was found to be highly effective for both serum stability and antimicrobial activity.
The immune response generated against these chimeric peptides was found to be specific to the respective B-cell epitopes.
The purity of the peptides was found to be > 95%.
No correlation between intestinal permeability and GI peptides was found.
A total of 85.7% of all quantified peptides was found in these fractions.
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CEO of Professional Science Editing for Scientists @ prosciediting.com