ライフサイエンスコーパス: critical micelle concentration

1 onium) head groups, both below and above the critical micelle concentration.

2 ecyl sulfate is not due to a decrease in the critical micelle concentration.

3 ation of elongated rod-like micelles above a critical micelle concentration.

4 ven at concentrations far in excess of their critical micelle concentration.

5 rly, the detergent must be present above its critical micelle concentration.

6 se short chain phosphatidylcholine below the critical micelle concentration.

7 vesicles, with a maximum rate reached at the critical micelle concentration.

8 ar aggregates are apparently formed near the critical micelle concentration.

9 se linearly with SDS concentration above the critical micelle concentration.

10 partition ratios, salting out constants, and critical micelle concentrations.

11 remarkably high Krafft temperatures, and low critical micelle concentrations.

12 nd several other detergents well below their critical micelle concentrations.

13 lpha-synuclein-dependent depression of their critical micelle concentrations.

14 a profound, taudependent depression of their critical micelle concentrations.

15 resence of surfactants, especially above the critical micelle concentration (a feature of regular det

16 E-PEG), which forms 12-nm micelles above the critical micelle concentration, accumulates heavily insi

17 ts are thoroughly characterized to determine critical micelle concentration, aggregation number, pola

18 Ls are thoroughly characterized to determine critical micelle concentration, aggregation number, pola

19 d, at detergent concentrations exceeding the critical micelle concentration, although these matrix co

20 nis are water soluble and form micelles with critical micelle concentrations an order of magnitude lo

21 to its periphery all had an influence on the critical micelle concentration and the micelle size.

22 The critical micelle concentration and the micellization deg

23 1-40) or Nalpha-OA-Abeta, as shown by lower "critical micelle concentrations" and higher monolayer co

24 onionic lipid mimicking detergent, above its critical micelle concentration ( approximately 0.7% at 2

25 acking calorimetric data, measurement of the critical micelle concentration at a single temperature s

26 The detergent interaction starts below the critical micelle concentration at a well-defined mixed h

27 tes does not show an anomalous change at the critical micelle concentration because the enzyme is pre

28 rsection is used to dilute the SDS below its critical micelle concentration before the detection poin

29 0 or Triton X-100) are increased up to their critical micelle concentrations, beyond which activity d

30 chain phosphatidylcholines, far below their critical micelle concentration, by phospholipase A2 (PLA

31 At concentrations well below its critical micelle concentration, C6PS binding to bovine F

32 (DAF), polysorbate concentrations above the critical micelle concentration can be quantified by the

33 se of Fos-Choline-12 concentration above the critical micelle concentration causes a transition to a

34 reveal an unusually gradual decrease in log critical micelle concentration (CMC) as the chain length

35 tions were all well described below the C6PS critical micelle concentration (CMC) by this activation

36 pH 4.0 (nonionic), all diastereomers have a critical micelle concentration (CMC) in the micromolar r

37 The critical micelle concentration (cmc) of ent-DCA, determi

38 ped curve with its maximum activity near the critical micelle concentration (CMC) of nonionic deterge

39 The critical micelle concentration (CMC) of Reb A was found

40 reduction stoichiometry increases up to the critical micelle concentration (CMC) of SDS, where it re

41 AH porewater concentration occurred when the critical micelle concentration (CMC) of the IL was excee

42 f the liposomes and for determination of the critical micelle concentration (cmc) of the ILs.

43 A method for determining the critical micelle concentration (CMC) of various detergen

44 at concentrations below their corresponding critical micelle concentration (cmc) values were determi

45 ity, and an inflection point designating the critical micelle concentration (CMC) was clearly visible

46 Below the critical micelle concentration (CMC), Bcl-x(L) binds det

47 pse when the TX100 concentration reached the critical micelle concentration (CMC), in the range of 0.

48 nts, at concentrations much greater than the critical micelle concentration (CMC), the fluorescence a

49 Above the critical micelle concentration (cmc), the hydrolysis rat

50 s; when its concentration is found below the critical micelle concentration (CMC), the matrix modifie

51 e bulk lysoPC concentration is less than its critical micelle concentration (CMC), we observe a compr

52 ne (DVB), and a photo-cross-linker above its critical micelle concentration (CMC).

53 solutions when the surfactant was below its critical micelle concentration (CMC).

54 oaches at concentrations below and above the critical micelle concentration (cmc).

55 inimum thermal conductivity occurring at the critical micelle concentration (CMC): the thermal conduc

56 MS) using conventional surfactant [above the critical micelle concentration (cmc)] is very challengin

57 The critical micelle concentrations (cmc) decrease with incr

58 The absolute surface tension curves and critical micelle concentrations (CMC) determined for the

59 Critical micelle concentrations (CMC) of these assemblie

60 , median effective concentrations (EC50) and critical micelle concentrations (CMC) were determined.

61 owed an abrupt break (routinely taken as the critical micelle concentration, CMC) at 2.9 mM.

62 ine (N-NBD-MPE), at concentrations below its critical micelle concentration (CMCN-NBD-MPE = 4 microM)

63 e compounds leads to aggregation above their critical micelle concentrations (CMCs), which may be imp

64 These siderophores have low critical micelle concentrations (CMCs).

65 entrations orders of magnitude below the SDS critical micelle concentration demonstrated that SWNTs r

66 both quercetin and pyrene reported a higher critical micelle concentration for bile salts than for S

67 ergents, at concentrations up to twice their critical micelle concentrations, from the nonionic class

68 e micelles, and experimentally determine the critical micelle concentration in solutions of hIAPP fra

69 MNG-3, which has a critical micelle concentration in the nanomolar regime,

70 These polypeptide micelles display a critical micelle concentration in the range 4-8 microM d

71 ed to aqueous-phase concentrations below the critical micelle concentration in the soil-slurry system

72 nto micelles at low concentrations and their critical micelle concentrations in phosphate buffered sa

73 h amphiphiles of opposite charge above their critical micelle concentration is the propensity for agg

74 e experimental temperature dependence of the critical micelle concentration is then good.

75 m alkyl sulfates at concentrations above the critical micelle concentration leads to a non-Nernstian

76 und with large countercurrent mobility, zero critical micelle concentration, low aggregation number,

77 on of 40 microM, which is much less than the critical micelle concentration of 0.4 mM.

78 All three techniques yield a critical micelle concentration of 3-3.5 micro M peptide.

79 rface to form a 20 A thick film and showed a critical micelle concentration of approximately 120 nM.

80 Complex assembly occurs well below the critical micelle concentration of C6PS, as established i

81 nt column, or by rapid dilution to below the critical micelle concentration of detergent followed by

82 NMR of uniformly-(15)N-labeled EqtII at the critical micelle concentration of dodecylphosphocholine,

83 ne-NaC ratio in aqueous solution rather than critical micelle concentration of NaC, and the good disp

84 re chosen based on CMC/200, where CMC is the critical micelle concentration of the surfactants.

85 Critical micelle concentrations of the enantiomeric bile

86 Lipid critical micelle concentration set the limitation to the

87 tions almost an order of magnitude below its critical micelle concentration, suggest a mechanism of i

88 BCPs* in toluene solution is higher than the critical micelle concentration, suggesting a twisting an

89 esence of surface-active compounds below the critical micelle concentration; this is a newly observed

90 Critical micelle concentration values of 1 nM, measured

91 ition ability with enhanced sensitivity, low critical micelle concentration values, and dual-drug del