ライフサイエンスコーパス: CTAB

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

2 lecule in association with approximately 270 CTAB molecules.

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

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

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

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

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

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

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

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

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

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

13 lages vary depending on metal precursors and CTAB concentration.

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

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

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

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

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

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

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

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

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

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

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

25 presence of cetyltrimethylammonium bromide (CTAB) surfactant.

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

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

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

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

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

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

32 ic detergent cetyltrimethylammonium bromide (CTAB).

33 presence of cetyltrimethylammonium bromide (CTAB).

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

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

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

37 in reverse micelles formed with the cationic CTAB surfactant.

38 ightly packed cetyltrimethylammoniumbromide (CTAB) bilayer.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 clearly demonstrated superiority of kit over CTAB extraction.

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

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

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

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

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

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

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

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

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

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

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

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

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

82 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

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

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

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

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

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

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

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

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

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

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

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

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