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1 four to five orders of magnitude below their critical micelle concentration.
2 ecyl sulfate is not due to a decrease in the critical micelle concentration.
3 onium) head groups, both below and above the critical micelle concentration.
4 ation of elongated rod-like micelles above a critical micelle concentration.
5 ven at concentrations far in excess of their critical micelle concentration.
6 rly, the detergent must be present above its critical micelle concentration.
7 se short chain phosphatidylcholine below the critical micelle concentration.
8 vesicles, with a maximum rate reached at the critical micelle concentration.
9 ar aggregates are apparently formed near the critical micelle concentration.
10 se linearly with SDS concentration above the critical micelle concentration.
11 partition ratios, salting out constants, and critical micelle concentrations.
12 remarkably high Krafft temperatures, and low critical micelle concentrations.
13 nd several other detergents well below their critical micelle concentrations.
14 lpha-synuclein-dependent depression of their critical micelle concentrations.
15 a profound, taudependent depression of their critical micelle concentrations.
16 resence of surfactants, especially above the critical micelle concentration (a feature of regular det
17 E-PEG), which forms 12-nm micelles above the critical micelle concentration, accumulates heavily insi
18 ts are thoroughly characterized to determine critical micelle concentration, aggregation number, pola
19 Ls are thoroughly characterized to determine critical micelle concentration, aggregation number, pola
20 d, at detergent concentrations exceeding the critical micelle concentration, although these matrix co
21 nis are water soluble and form micelles with critical micelle concentrations an order of magnitude lo
22 to its periphery all had an influence on the critical micelle concentration and the micelle size.
24 ntrations were significantly below published critical micelle concentrations and constituted <0.1% of
25 s can significantly influence the surfactant critical micelle concentrations and the surface excess v
26 1-40) or Nalpha-OA-Abeta, as shown by lower "critical micelle concentrations" and higher monolayer co
27 onionic lipid mimicking detergent, above its critical micelle concentration ( approximately 0.7% at 2
28 acking calorimetric data, measurement of the critical micelle concentration at a single temperature s
29 The detergent interaction starts below the critical micelle concentration at a well-defined mixed h
30 tes does not show an anomalous change at the critical micelle concentration because the enzyme is pre
31 rsection is used to dilute the SDS below its critical micelle concentration before the detection poin
32 0 or Triton X-100) are increased up to their critical micelle concentrations, beyond which activity d
33 chain phosphatidylcholines, far below their critical micelle concentration, by phospholipase A2 (PLA
35 (DAF), polysorbate concentrations above the critical micelle concentration can be quantified by the
36 se of Fos-Choline-12 concentration above the critical micelle concentration causes a transition to a
37 reveal an unusually gradual decrease in log critical micelle concentration (CMC) as the chain length
38 LPG strongly induces fibrillation around its critical micelle concentration (cmc) by promoting format
39 tions were all well described below the C6PS critical micelle concentration (CMC) by this activation
40 pH 4.0 (nonionic), all diastereomers have a critical micelle concentration (CMC) in the micromolar r
42 (O/W) emulsions at concentrations above its critical micelle concentration (cmc) of 0.6 mm, but also
43 trate greater colloidal stability with a low critical micelle concentration (CMC) of 80.3 nM, larger
44 tability of O/W emulsions by influencing the critical micelle concentration (CMC) of cetyltrimethylam
46 ped curve with its maximum activity near the critical micelle concentration (CMC) of nonionic deterge
48 reduction stoichiometry increases up to the critical micelle concentration (CMC) of SDS, where it re
49 AH porewater concentration occurred when the critical micelle concentration (CMC) of the IL was excee
52 emperature (T(k) < 5 degrees C) and a higher critical micelle concentration (CMC) than its nonionic c
53 c strength, and temperature conditions, with critical micelle concentration (CMC) values in the low m
54 at concentrations below their corresponding critical micelle concentration (cmc) values were determi
55 ity, and an inflection point designating the critical micelle concentration (CMC) was clearly visible
59 pse when the TX100 concentration reached the critical micelle concentration (CMC), in the range of 0.
60 rogen-bonding surfactant C12E6, close to the critical micelle concentration (CMC), induces a drastic
61 dium dodecyl sulfonate (SDS) were lower than critical micelle concentration (CMC), lipid oxidation pr
63 nts, at concentrations much greater than the critical micelle concentration (CMC), the fluorescence a
65 s; when its concentration is found below the critical micelle concentration (CMC), the matrix modifie
66 Milspec AFFF, which was above the mixture's critical micelle concentration (CMC), was at application
67 e bulk lysoPC concentration is less than its critical micelle concentration (CMC), we observe a compr
68 t transfer enhancement is optimized near the critical micelle concentration (CMC), which is an equili
75 inimum thermal conductivity occurring at the critical micelle concentration (CMC): the thermal conduc
76 MS) using conventional surfactant [above the critical micelle concentration (cmc)] is very challengin
80 , median effective concentrations (EC50) and critical micelle concentrations (CMC) were determined.
82 ine (N-NBD-MPE), at concentrations below its critical micelle concentration (CMCN-NBD-MPE = 4 microM)
83 e compounds leads to aggregation above their critical micelle concentrations (CMCs), which may be imp
86 entrations orders of magnitude below the SDS critical micelle concentration demonstrated that SWNTs r
87 urface, a betaine side chain and an ultralow critical micelle concentration, enabling drug penetratio
88 The peptide thioesters, above or below their critical micelle concentrations, enter cells mainly via
89 both quercetin and pyrene reported a higher critical micelle concentration for bile salts than for S
90 ergents, at concentrations up to twice their critical micelle concentrations, from the nonionic class
91 e micelles, and experimentally determine the critical micelle concentration in solutions of hIAPP fra
94 ed to aqueous-phase concentrations below the critical micelle concentration in the soil-slurry system
95 nto micelles at low concentrations and their critical micelle concentrations in phosphate buffered sa
96 h amphiphiles of opposite charge above their critical micelle concentration is the propensity for agg
98 m alkyl sulfates at concentrations above the critical micelle concentration leads to a non-Nernstian
99 und with large countercurrent mobility, zero critical micelle concentration, low aggregation number,
102 amperes of current and about 0.015 times the critical micelle concentration of an ionic surfactant.
103 rface to form a 20 A thick film and showed a critical micelle concentration of approximately 120 nM.
105 nt column, or by rapid dilution to below the critical micelle concentration of detergent followed by
106 NMR of uniformly-(15)N-labeled EqtII at the critical micelle concentration of dodecylphosphocholine,
107 ompanied by MAG/DOPC had lower values of the critical micelle concentration of hydroperoxides and lar
108 ne-NaC ratio in aqueous solution rather than critical micelle concentration of NaC, and the good disp
112 tions almost an order of magnitude below its critical micelle concentration, suggest a mechanism of i
113 BCPs* in toluene solution is higher than the critical micelle concentration, suggesting a twisting an
114 ation in the subphase reaches or exceeds its critical micelle concentration, the surface tension, gam
115 esence of surface-active compounds below the critical micelle concentration; this is a newly observed
117 ition ability with enhanced sensitivity, low critical micelle concentration values, and dual-drug del
118 Lecithin at a level (500 ppm) lower than its critical micelle concentration was able to protect the l
119 ions and a drastic shift in the surfactants' critical micelle concentration, which we show can be use