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1 hyl phosphate (DEP), and a product analogue, cacodylate.
2 t higher ionic strength than in 10 mM sodium cacodylate.
3 ion: Tris, bis-Tris propane, Tes, Hepes, and cacodylate.
4 lar structure is observed in the presence of cacodylate.
5 HIV-1) crystallized in the absence of sodium cacodylate.
6 ly(dA).poly(dT) and (dA)20.(dT)20 in a 50 mM cacodylate, 0.1 M NaCl, pH 7 buffer by using the time-co
10 in is predominantly unfolded in 10 mM sodium cacodylate at neutral pH based on circular dichroism and
14 hase vanishes upon increasing [Na(+)] in the cacodylate buffer, and the kinetics switch completely fr
18 obility of a double-stranded DNA oligomer in cacodylate-buffered solutions containing various concent
19 e structure of the protein in the absence of cacodylate exhibits significant deviations from the prev
20 tes of the thioredoxin relay mechanism and a cacodylate molecule mimicking the substrate interactions
21 2+), Mn(2+)or Mg(2+)and 2-mercaptoethanol in cacodylate or HEPES buffer, pH 7.2, exhibits the ability
22 Crystal structures of LpxC complexed with cacodylate or palmitate demonstrate that both Glu78 and
23 We also demonstrate that in the absence of cacodylate this protein will bind to Mg2+, and could pro
24 buted to the modification of C65 and C130 by cacodylate, which was an essential component of the orig
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