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The authors also showed that the above-mentioned Co Ag interaction is suppressed after axial coordination of NO to the cobalt porphyrin and suggested that this effect results from competition between the two axial ligands (NO and the silver surface, considered as a point ligand).
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The frequency of specific interactions was suppressed by adding free BSA.
Interactions were suppressed by methionine (75 µM) [26], [27].
Interactions were suppressed by supplementing SC medium with methionine (Fig. 3C).
Non-specific interactions were suppressed with 5% fetal bovine serum (FBS) in permeabilization buffer (0.2% tween-20, 0.5% Triton X-100 in PBS pH 7.0) for 30 minutes and then samples were incubated with primary antibodies anti-PLN 1D11 and anti-COP I in permeabilization buffer.
Second, our data suggest that longer path length interactions are suppressed at higher spatial frequencies.
These interactions are suppressed by defense-related stimuli and enhanced by prolonged exposure to constant light.
Moreover, intermolecular electron spin spin interactions were suppressed by properly diluting the labeled protein with the wild type (wt) during fibril formation.
A protein-protein interaction network (PIN) was suggested to be a disassortative network, in which interactions between high- and low-degree nodes are favored while hub-hub interactions are suppressed.
When the SA level is intermediate, the interaction between NPR1 and NPR3 is suppressed, leading to the accumulation of NPR1, and activating the SA-dependent defense genes (Caarls et al. 2015).
WRN exonuclease activity is suppressed by interaction with p53 (Brosh et al 2001a) or BLM (von Kobbe et al 2002) and stimulated by interaction with Ku70/80 (Li and Comai 2001) or phosphorylation (Karmakar et al 2002).
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