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After inactivation of endogenous peroxidase with 3%H2O22, the sections were blocked with goat serum and incubated with primary antibody.
However, an inhibiting ability is partially kept in all the strains under study even after inactivation of hydrogen peroxide by catalase.
In pathophysiological conditions, PS and PE are shuttled to the outer leaflet after inactivation of the aminophospholipid translocase or flippase, and activation of the Ca2+-dependent ATP-independent scramblase.
After inactivation of the natural diheme cofactor of MauG, it was shown that the Co2 +-loaded 6 × His-tag could substitute for the hemes in the H2O2-driven catalysis of tryptophan tryptophylquinone biosynthesis.
PE and PS are externalised to the outer leaflet of the cell membrane after inactivation of aminophospholipid translocase or flippase and activation of scramblase, another Ca2+-dependent ATP-independent enzyme [19, 20]. Figure 1 Phospholipid bilayer composed of hydrophobic non-polar tails and hydrophilic polar heads.
After inactivation of virB, expression of some proteins associated with iron metabolism was changed.
After inactivation of virB, the greatest protein expression change was observed in the outer membrane proteins.
Nevertheless, persistent outward currents were observed at positive potentials after inactivation of the Na+ current (e.g. Figure 2).
Growth kinetics of C. jejuni after inactivation of pyruvate kinase by Tween 20 was performed as described [25].
Particularly relevant to the experiments shown in figure 6, is the identity of the system that determines the rapid exit of ERK after inactivation of MEK activity.
The ability to induce the production of the cytokines IL-1β, IL-6 and TNF-α was also compromised after inactivation of oppD.
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