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1 ount (moles) vs. its concentration in water (molarity).
2 folds exhibiting notable values of effective molarity.
3  concentrated, resulting in a high effective molarity.
4 ressed in the large differences in effective molarity.
5 correlated well with the reduction of buffer molarity.
6 ding the helix, are allowed to vary with TFE molarity.
7 lly modified histone peptides mixed in equal molarity.
8 cid, ammonia, and ammonia salts with varying molarity.
9  The inputs to SPT are the solvent radii and molarities.
10 stigating various parameters, such as buffer molarity (0.1-1 M), temperature (25 degrees C-90 degrees
11 ither 0.1% trifluoroacetic acid (TFA) or low-molarity (100, 50, 20, and 5 mM) ethylenediaminetetraace
12 strate guests, leading to a larger effective molarity (amplification), and an increase in the rate ac
13           The relationship between effective molarity and intervening nucleic acid secondary structur
14 l relationship interconverting the scales of molarity and molality without requiring the density of t
15 e, tetrabutylammonium bromide concentration, molarity, and solvent polarity on the resolution rate, p
16  structure is required to maximize effective molarities between reactants, possibly by compacting int
17                          Reduction of buffer molarity by dilution also resulted in exposure of the fu
18 A, we determine the dependence of the solute molarity (C3) on that of BSA (C2) at fixed temperature (
19 inear dependence of ln <w> and DeltaH on TFE molarity can be used to extrapolate the results from 25%
20 ly, we found that IdU and CldU, when used at molarities comparable to those that label the maximal nu
21                   Recently, we developed low-molarity conductive media to mitigate this positive feed
22 ection in a dose-dependent manner and at low molarity despite absence of sequence similarity to filov
23        DMCs were used to determine effective molarities (EM) for the formation of intramolecular phen
24 tions allowed determination of the effective molarities (EM) for the intramolecular interactions.
25 pectively), reveals that while the effective molarities (EM)s are almost identical (EM(2m)) 26 M; EM(
26                                    Effective molarity (EM) is a key parameter that determines the eff
27  this mechanism, with an estimated effective molarity (EM) of the general base of >15 M, consistent w
28 the two reactants, resulting in an effective molarity (EM) of ~40 M.
29 ate cooperativities attained, with effective molarity (EM) values reaching record values over 10(3) M
30 ally bound states to determine the effective molarities for the intramolecular interactions by compar
31                                    Effective molarities for the subsequent unimolecular N-alkylation
32             Surprisingly, the mean effective molarity for binding the flexible alpha-cyclodextrin-bas
33          The monolayer provides an effective molarity for the reaction of approximately 500 M as comp
34                           An alternate, high-molarity, high-temperature ('HighMT') protocol has been
35  decreasing variation in mobility with pH as molarity increases.
36 ed to the later value, dehydratase effective molarity is 11 M.
37  of ca. 10(38) M(-1), and the mean effective molarity is ca. 830 M.
38                                The effective molarity is calculated to be 230 M by comparison of k(u)
39                         A higher electrolyte molarity is found to enhance the capacity utilization dr
40      Our analysis reveals that the effective molarity is the critical parameter in optimizing the bro
41 cular association constant and the effective molarity KEM > 1, there is a linear increase in the free
42 ide in the presence of cysteine at the micro-molarity level.
43  treatment requires hours of exposure to low-molarity, low-temperature bisulfite ('LowMT') and, somet
44 ain association, represented by an effective molarity (M(eff)), is maximal for a linker extended by o
45 eports dissociation constants and "effective molarities" (M(eff)) for the intramolecular binding of a
46                      In principle, effective molarity measurements, in which exogenous acids/bases re
47 uimolar mixtures, and two-component variable molarity mixtures.
48 ose responses to either N-moles, W-volume, N-molarity (N/W), or their synergistic interaction (NxW).
49              We obtained consensus effective molarities of approximately 5 x 10(4) M for KSI from Com
50 ) groups) gave quantitative estimates of the molarities of interfacial bromide (Br(m)) and water (H(2
51 on-Crick base pairing controls the effective molarities of substrates tethered to DNA strands; bond-f
52  base-pairing interaction, and the effective molarities of the intramolecular interactions in the dup
53 or of the antibody complex with an effective molarity of 76.7 M, revealing a significant catalytic be
54 pecimens for the variable parameters such as molarity of alkaline solution, Flyash/GGBS ratio and par
55       We developed an approach to obtain the molarity of any structurally enriched semiconducting sin
56 t higher oil and surfactant contents, higher molarity of CaCl2 and lower alginate concentrations.
57 sts in 3.5-fold molar excess relative to the molarity of ExbD in E. coli suggests the possibility of
58 n of the recovered oil bodies depends on the molarity of medium used; the use of a sodium bicarbonate
59                                         Also Molarity of NaOH are tested from 8 to 14 M and both the
60 lease rate were identified, including pH and molarity of quench buffer.
61 cal reactions through increases in effective molarity of reactants.
62 culated based on particle size, density, and molarity of the analyte within solution.
63 n seed and mass of media during grinding and molarity of the medium used on oil body integrity, purit
64 ced proximity (SIP) amounted to an effective molarity of ~10-30 muM for the binding partners.
65                               The "effective molarity" of the cationic side chain of Arg-235 at the w
66     Here we addressed this problem using low-molarity solutions of ethylenediaminetetraacetic acid (E
67                     Thus, the high effective molarities suggest a large catalytic contribution associ
68  the effects of current density, electrolyte molarity, temperature, and oxygen purity on the performa
69 no effect on artifact MMHg for each leachate molarity tested.
70  filling available RPF with sugar to achieve molarities that balance reasonable tensions over starch
71  positioning effects and determine effective molarities that estimate catalytic contributions.
72 s dispersed in solutions with different salt molarity that the diffusion of nanoparticles increases w
73 cyc-CxC*AyA) dimers, thus enabling effective molarities to be estimated for the various systems.
74 under alkaline conditions, with an effective molarity up to 2900 M for the imidazolyl group, ruling o
75  anthocyanins (using the optimal tannic acid molarity) were spray-dried with either maltodextrin alon
76 ty was maximized close to physiological salt molarities while processivity was midrange at physiologi
77 e presence of only 1% Pb(2+) (versus K(+) by molarity), while the permeability of Pb(2+) is independe
78 ble over a range of buffer concentration and molarity, with no evidence of temporal degradation over
79  strategy relies on adjusting the co-solvent molarity without the need to adjust the back-pressure re