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1 as well as N-(2-hydroxyethyl)piperazine-N'-2-ethanesulfonic acid (HEPES) and benzoate are also presen
3 ) in 0.1 M N-(2-hydroxyethyl)piperazine-N'-2-ethanesulfonic acid (HEPES) buffer in the presence of 0.
5 zwitterion, N-2-hydroxyethylpiperazine- N'-2-ethanesulfonic acid (HEPES), facilitates the formation a
6 selenophosphoramide derived from BINAM, and ethanesulfonic acid as a cocatalytic Bronsted acid induc
7 hydroxymethyl)-aminomethane/2-(N-morpholino) ethanesulfonic acid buffer, both COR6.6 and COR15am inva
9 ent of Cl(-) by gluconate or 2-(N-morpholino)ethanesulfonic acid decreased the apparent affinity of G
10 m = 9.37 +/- 0.02; and piperazine-N,N'-bis(2-ethanesulfonic acid) (Pipes) for which log Ka1m = 2.81 +
11 ation in 10 and 100 mM piperazine-N,N'-bis(2-ethanesulfonic acid) (Pipes), 1 mM MgSO4, and 2 mM [ethy
12 istics in vitro: 20 mM piperazine-N,N'-bis(2-ethanesulfonic acid) (PIPES), 100 mM NaCl, 10 mM dithiot
13 formed in N-(2-hydroxyethyl)piperazine-N'-(2-ethanesulfonic acid) buffer with microwave heating and p
14 fied Hepes (N-2-hydroxyethylpiperazine-N'-2- ethanesulfonic acid)-buffered medium (pH(o) 6.8) resulte
15 ene oxide dimer acid (HFPO-DA aka GenX), and ethanesulfonic acid, 2-[1-[difluoro(1,2,2,2-tetrafluoroe
18 ), Hepes (N-[2-hydroxyethyl]piperazine-N'-[2-ethanesulfonic acid]), Bes (N,N-bis[2-hydroxyethyl]-2-am
20 herbicide dimethenamid, and their respective ethanesulfonic (ESA) and oxanillic (OA) acid degradates