ライフサイエンスコーパス: CTAB

1 The formulation containing 10 % CTAB-Mt (P2BO10) showed significant enhancements in wate

2 itrate, CuCl(2), proline, xylitol, NDSB 201, CTAB and K(2)PO(4)) solubilized more than one of the 41

3 lecule in association with approximately 270 CTAB molecules.

4 A from olive, sunflower and palm oils, and a CTAB-based method was selected.

5 Adding an oil, i.e., decane, into a CTAB-EtOH-TEOS ammonia solution leads to thin-film forma

6 ction method from pollen in honey based on a CTAB buffer-based DNA extraction using the Maxwell 16 in

7 ured silica filled with the templating agent CTAB and is shown to yield accurate images of the core-s

8 nce of soybean DNA, were not achieved in all CTAB extracts of DNA, while commercial kit gave satisfac

9 Also, CTAB micelles induced a marked increase in the helicity

10 rtrazine TZ- cetryltrimethyl ammoniumbromide CTAB as a chemical modifier TZ-CTA.

11 l conformation in the presence of Zn(2+) and CTAB micelles, and has allowed the stability of this rar

12 s work, vesicles composed of cholesterol and CTAB (1/1 mol %) or cholesterol and DOPC (2/8 mol %) and

13 Two types of cationic AuNPs, cysteamine and CTAB capped, were compared to achieve maximum assay perf

14 micelles, clear cross peaks between HPTS and CTAB in the 2D NMR spectra show that HPTS embeds in the

15 ini kit (Qiagen), Furtado (2014) method, and CTAB-LiCl method.

16 lages vary depending on metal precursors and CTAB concentration.

17 the aqueous phase of Tween 20-stabilized and CTAB-stabilized emulsions, respectively.

18 ization revealed strong interactions between CTAB and PFAS, which spontaneously formed positively cha

19 Moreover, substantial amounts of both CTAB and Tween distributed into the KTP-rich phase from

20 lized with cetyl trimethyl ammonium bromide (CTAB) led to formation of gold aggregates and a red to b

21 nd without cetyl trimethyl ammonium bromide (CTAB), a surfactant, and meso-tetrakis(pentafluorophenyl

22 leaved with cethyltrimethylammonium bromide (CTAB) at regular intervals, thus giving rise to a lamell

23 g different substances: cetrimonium bromide (CTAB) cationic surfactant, isopropyl alcohol premixed wi

24 ion (CMC) of cetyltrimethylammonium bromide (CTAB) and the distribution of lipid hydroperoxides and a

25 aining 25 mM cetyltrimethylammonium bromide (CTAB) at pH 9.50 was used as a background electrolyte.

26 presence of cetyltrimethylammonium bromide (CTAB) into a 125muL volume of 1-butyl-3-methylimidazoliu

27 coating with cetyltrimethylammonium bromide (CTAB) is shown to provide reproducible electroosmotic fl

28 od, in which cetyltrimethylammonium bromide (CTAB) is used to extract nucleic acids from plant tissue

29 , a modified Cetyltrimethylammonium Bromide (CTAB) Method, Alkaline Method, Urea Method, Salt Method,

30 tabilized by cetyltrimethylammonium bromide (CTAB) micelles and Zn(2+).

31 lf-assembled cetyltrimethylammonium bromide (CTAB) molecules are used to control interfaces in a core

32 ocedure, the cetyltrimethylammonium bromide (CTAB) procedure, and the Reacti-Bind procedure.

33 presence of cetyltrimethylammonium bromide (CTAB) surfactant.

34 c surfactant cetyltrimethylammonium bromide (CTAB) under UV irradiation to enhance e(aq)(-) utilizati

35 Cetyltrimethylammonium bromide (CTAB) was employed as ion-pairing agent to enhance the h

36 surfactant (cetyltrimethylammonium bromide (CTAB)) was used in each case and micelle formation was c

37 addition of cetyltrimethylammonium bromide (CTAB), a surfactant, induced oscillatory behavior and si

38 of cationic, cetyltrimethylammonium bromide (CTAB), and anionic, sodium dodecyl sulfate (SDS), surfac

39 lfate (SDS), cetyltrimethylammonium bromide (CTAB), and polyoxyethylene sorbitan monooleate (Tween 80

40 tal halides, cetyltrimethylammonium bromide (CTAB), and thiourea (Tu).

41 e absence of cetyltrimethylammonium bromide (CTAB), NiMP-11 is aggregated.

42 surfactant, cetyltrimethylammonium bromide (CTAB), on the LC surface.

43 surfactants cetyltrimethylammonium bromide (CTAB), or hexadecylamine (HDA).

44 micelles of cetyltrimethylammonium bromide (CTAB), photolysis of FePPIX-CO induces a complicated set

45 ic detergent cetyltrimethylammonium bromide (CTAB).

46 presence of cetyltrimethylammonium bromide (CTAB).

47 For cetyltrimethylammonium bromide (CTAB)/sodium octyl sulfonate catanionic vesicles, K =.7

48 surfactant, cetyl trimethylammonium bromide (CTAB), and the photoresponsive organic derivative, trans

49 surfactant, cetyl trimethylammonium bromide (CTAB), when 5-methyl salicylic acid (5mS) is added at sl

50 ion-pairing (cetyltrimethylammonium bromide, CTAB) for the determination of iodide in table salt has

51 h amine (trimethyloctadecylammonium bromide, CTAB) and carboxyl (stearic acid, SA) functional groups.

52 The adsorption of Cr(VI) by CTAB- and SA-coated nanoparticles increased with decreas

53 charges of aqueous drops containing cationic CTAB, anionic SDS, and neutral C(8)E(3) sliding on diffe

54 in reverse micelles formed with the cationic CTAB surfactant.

55 ate and 0.2 g cetyltrimethylammoniumbromide (CTAB) and a cationic surfactant (drop-wise).

56 ightly packed cetyltrimethylammoniumbromide (CTAB) bilayer.

57 atic interactions between positively charged CTAB and anionic Cr(VI) species.

58 d to the CF-based method in the case of Chol/CTAB vesicles, which can suffer from lipid demixing duri

59 ) reinforced with organically modified clay (CTAB-Mt) at varying concentrations to improve barrier an

60 The effects of pH, buffer concentrations, CTAB concentration, and the operation voltages on the se

61 Comparison with the corresponding CTAB/water/alcohol system (prepared without silica) show

62 ase of sp-cit-Au NPs, sp-CTAB-Au NPs, and cu-CTAB-Au NPs.

63 cube-like CTAB-capped gold nanoparticles (cu-CTAB-Au NPs) as cores.

64 The LOD of the cu-CTAB-Au NPs is therefore approximately 340 times below t

65 same comparison showed that the ERLs with cu-CTAB-Au NPs as cores were close to 200 times more sensit

66 ectron generator whereas the high dielectric CTAB/PVDF (~ 400) is used as dielectric separator cum st

67 ric polymer film has been prepared by doping CTAB in PVDF matrix via solution casting method.

68 bromide polyacrylamide gel electrophoresis (CTAB-PAGE), for subsequent electrophoretic probing with

69 ses with the concentration of 5mS at a fixed CTAB content.

70 an square deviation for kit is 0.208 and for CTAB is 2.127, clearly demonstrated superiority of kit o

71 However, for CTAB and sodium perfluorooctanoate (FC(7)) vesicles, K =

72 nce of E. coli dissociates the aptamers from CTAB and restores the dark signal induced by the surfact

73 persed assemblies containing several hundred CTAB molecules, indicating the coalescence of the micell

74 issolution of faceted platelets with Au(III)/CTAB complex that transforms them into smaller nanodisks

75 In CTAB micellar solutions, where aggregation of NiMP-11 do

76 In CTAB reverse micelles, clear cross peaks between HPTS an

77 a 50% TFE solution (K(d) = 3.1 x 10(-4) M in CTAB and 2.3 x 10(-4) M in TFE).

78 ant and oxidation parameters was not seen in CTAB-stabilized emulsions.

79 nanoparticles (sp-CTAB-Au NPs), or cube-like CTAB-capped gold nanoparticles (cu-CTAB-Au NPs) as cores

80 compared the optimised method with a manual CTAB buffer-based DNA isolation method.

81 ontrast to the original method, the modified CTAB procedure is faster, omits the selective precipitat

82 onium bromide-stabilized gold nanoparticles (CTAB-AuNPs).

83 In this reactor, the addition of CTAB (cetrimonium bromide, a cationic surfactant) caused

84 ing 1 % NaCl with 1 % KCl changed the CMC of CTAB significantly but not with 171 mM KCl (the same mol

85 array fabrication, and the concentration of CTAB has a significant effect on oligo immobilization ef

86 r ligand exchange to achieve displacement of CTAB on nanorods.

87 selected protocols: the in-house methods of CTAB-PVP (cetyltrimethylammonium bromide-polyvinylpyrrol

88 nfiguration of the mixed hemi/ad-micelles of CTAB at Mag-NPs, zeta-potential measurements were perfor

89 Aqueous mixtures of CTAB and OMCA in basic solution self-assemble into long,

90 Luminescence is quenched in the presence of CTAB and enhanced in the presence of SDS, both in a pH-d

91 analysis illustrated the crystalline size of CTAB capped TiO(2), MoS(2)@TiO(2) and L-Cysteine capped

92 The size of CTAB/FC7 bicelles is observed to evolve with the additio

93 The use of CTAB as a short-term (5-8 day) storage buffer, followed

94 The use of CTAB resulted in mesoporous powders, whereas HDA yielded

95 The DNA extraction method based on CTAB-phenol-chloroform was best for walnut.

96 The DNA extraction method based on CTAB-phenol-chloroform was the best for hazelnut.

97 clearly demonstrated superiority of kit over CTAB extraction.

98 electrolyte to the sodium perfluorooctanoate/CTAB vesicles leads to vesicles with two bilayers; the a

99 onstrate pan-analyte immobilization of sized CTAB-laden model proteins (protein G, ovalbumin, bovine

100 spherical CTAB-capped gold nanoparticles (sp-CTAB-Au NPs), or cube-like CTAB-capped gold nanoparticle

101 f human IgG in the case of sp-cit-Au NPs, sp-CTAB-Au NPs, and cu-CTAB-Au NPs.

102 The ERLs fabricated with sp-CTAB-Au NPs as cores proved to be more than 50 times mor

103 old nanoparticles (sp-cit-Au NPs), spherical CTAB-capped gold nanoparticles (sp-CTAB-Au NPs), or cube

104 e suspensions in the presence of submicellar CTAB, which acts as a surface passivator.

105 reaction conditions, the cationic surfactant CTAB and the nonionic one, Tween 80, were taken into con

106 centration (1 mM) of the cationic surfactant CTAB in mixtures of 10 M water in an organic solvent (dD

107 The study shows that the surfactant (CTAB) was almost completely removed by acid extraction.

108 The synthesized CTAB/ZnO NPs demonstrated exceptional properties: they w

109 The CTAB procedure performs well enough to use in array fabr

110 The CTAB-AuNPs were etched with NO(2)(-) to yield Au(3+), wh

111 troscopy and thermogravimetric analysis, the CTAB molecules adsorbed on the surface of a Au nanostruc

112 he Ni/PTFE coating described before, but the CTAB failed to co-deposit the polymer.

113 e Co(3)O(4) nanooxide was synthesized by the CTAB assisted hydrothermal technique and was characteriz

114 rophobic environment that is provided by the CTAB micelle is found to be crucial to the native foldin

115 Protocol reported differs from the CTAB procedure by addition of higher concentration of sa

116 r affinity for Zn(2+) in the presence of the CTAB than in a 50% TFE solution (K(d) = 3.1 x 10(-4) M i

117 Cr(VI) adsorbed more strongly to the CTAB-coated nanoparticles than to the SA-coated material

118 iency than use of unmodified oligos with the CTAB procedure.

119 roposed as a good and greener alternative to CTAB in most cases.

120 ptide also bound Zn(2+) when it was bound to CTAB micelles, with Zn(2+) again inducing a decrease in

121 ape and position of plasmon peaks similar to CTAB-capped GNRs.

122 The structure of cholera toxin (CTAB(5)) bound to its putative ganglioside receptor, gal

123 ore and during the binding of cholera toxin (CTAB(5)) or its B-subunit (CTB(5)).

124 roved in-plane ordering over the full toxin (CTAB(5)) especially at low pH.

125 f GMO seed two extraction methods were used, CTAB and DNeasy Plant Mini Kit.

126 Using CTAB (cetyltrimethylammonium bromide) as the structure-d

127 us activated amides, from aldehydes by using CTAB-(t)BuOOH.

128 d hybrid power cell has been developed using CTAB/PVDF composite film in a sustainable manner.

129 through a facile self-assembly process using CTAB as the main template and TEOS as SiO2 precursor.

130 The UV/CTAB system demonstrated sustained performance across mu

131 Dynamic coating with CTAB can be used to eliminate electroosmosis or to rever

132 The combined use of HPMC with CTAB or Tween resulted in a further decrease in the ther

133 e scattering units in the cholera layer with CTAB(5) shortened after disulfide bond reduction of the

134 use of a surfactant, the catalyst made with CTAB had 50% higher catalytic activity, and that made wi