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Every maximal split torus of G is generically maximal split.
Let S ′ be a generically maximal split torus of G.
Since S is maximal split in G it is maximal split in the radical of Z G ( S ).
Since S is generically maximal split, S R p is a maximal split torus of G R p. Similarly for S R p ′. Now by [41, XXVI prop.
Since S is the maximal split torus of T then S K is the maximal split torus of T K = rad ( H K ) by Lemma 5.4.
As before, S ′ is also a maximal split torus of G.
Similar(11)
The spectrum for 14-SASL is dominated by an immobile component with a maximal hyperfine splitting of 64.6 G, compared to a smaller immobile component for 14-PCSL with a maximal splitting of 60.7 G.
The maximal splitting observed for 14-SASL bound to KcsA is comparable to that for 14-SASL bound to BSA, and because fatty acids bind to serum albumin in a number of deep pockets within the structure, this implies a buried site for binding of 14-SASL on KcsA.
Furthermore, if the same total amount of split-GFP constructs relative to intact Q73 GFP is expressed, then the maximal possible split-GFP fluorescence signal is only 50% of intact GFP.
The EPR spectrum for 14-SASL bound to KcsA shows a maximal hyperfine splitting greater than that observed for the spin-labeled phosphatidylcholine 14-PCSL in the presence of KcsA.
The Anaalac was assessed from the maximal PCr splitting in the contracting muscle: (3) An a alac = PCr · (1 − e − t / τ ) M, where Anaalac is the anaerobic alactic contribution, t is the exercise time, τ is time constant of the PCr splitting at the onset of exhausting exercise (23.4 s [ 30]), M is the body mass, and PCr is the phosphocreatine concentration at rest.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com