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1 concentrated, resulting in a high effective molarity.
2 folds exhibiting notable values of effective molarity.
3 ressed in the large differences in effective molarity.
4 correlated well with the reduction of buffer molarity.
5 ding the helix, are allowed to vary with TFE molarity.
6 The inputs to SPT are the solvent radii and molarities.
7 stigating various parameters, such as buffer molarity (0.1-1 M), temperature (25 degrees C-90 degrees
8 ither 0.1% trifluoroacetic acid (TFA) or low-molarity (100, 50, 20, and 5 mM) ethylenediaminetetraace
9 strate guests, leading to a larger effective molarity (amplification), and an increase in the rate ac
11 l relationship interconverting the scales of molarity and molality without requiring the density of t
12 e, tetrabutylammonium bromide concentration, molarity, and solvent polarity on the resolution rate, p
13 structure is required to maximize effective molarities between reactants, possibly by compacting int
15 A, we determine the dependence of the solute molarity (C3) on that of BSA (C2) at fixed temperature (
16 inear dependence of ln <w> and DeltaH on TFE molarity can be used to extrapolate the results from 25%
17 ly, we found that IdU and CldU, when used at molarities comparable to those that label the maximal nu
19 ection in a dose-dependent manner and at low molarity despite absence of sequence similarity to filov
21 tions allowed determination of the effective molarities (EM) for the intramolecular interactions.
22 pectively), reveals that while the effective molarities (EM)s are almost identical (EM(2m)) 26 M; EM(
24 this mechanism, with an estimated effective molarity (EM) of the general base of >15 M, consistent w
25 ally bound states to determine the effective molarities for the intramolecular interactions by compar
34 cular association constant and the effective molarity KEM > 1, there is a linear increase in the free
36 treatment requires hours of exposure to low-molarity, low-temperature bisulfite ('LowMT') and, somet
37 ain association, represented by an effective molarity (M(eff)), is maximal for a linker extended by o
38 eports dissociation constants and "effective molarities" (M(eff)) for the intramolecular binding of a
42 ) groups) gave quantitative estimates of the molarities of interfacial bromide (Br(m)) and water (H(2
43 on-Crick base pairing controls the effective molarities of substrates tethered to DNA strands; bond-f
44 or of the antibody complex with an effective molarity of 76.7 M, revealing a significant catalytic be
46 t higher oil and surfactant contents, higher molarity of CaCl2 and lower alginate concentrations.
47 sts in 3.5-fold molar excess relative to the molarity of ExbD in E. coli suggests the possibility of
48 n of the recovered oil bodies depends on the molarity of medium used; the use of a sodium bicarbonate
51 n seed and mass of media during grinding and molarity of the medium used on oil body integrity, purit
53 Here we addressed this problem using low-molarity solutions of ethylenediaminetetraacetic acid (E
58 under alkaline conditions, with an effective molarity up to 2900 M for the imidazolyl group, ruling o
59 ty was maximized close to physiological salt molarities while processivity was midrange at physiologi
60 ble over a range of buffer concentration and molarity, with no evidence of temporal degradation over
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