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1 in the presence of ionic detergents (SDS and cetyltrimethylammonium bromide).
2 ons, both of which arise from the surfactant cetyltrimethylammonium bromide.
3 ymerization in the presence of a surfactant, cetyltrimethylammonium bromide.
4 ecanoic acid and cetylpyridinium chloride or cetyltrimethylammonium bromide.
6 by sequentially coating with the surfactant cetyltrimethylammonium bromide and fluorous 1H,1H,2H,2H-
8 ve template system, comprising a surfactant (cetyltrimethylammonium bromide) and a chelating agent (c
9 ns were conducted with a catalytic amount of cetyltrimethylammonium bromide as phase-transfer agent a
12 the critical micelle concentration (CMC) of cetyltrimethylammonium bromide (CTAB) and the distributi
13 d a borate-phosphate buffer containing 25 mM cetyltrimethylammonium bromide (CTAB) at pH 9.50 was use
14 obic ternary complexes formed in presence of cetyltrimethylammonium bromide (CTAB) into a 125muL volu
15 sis in combination with dynamic coating with cetyltrimethylammonium bromide (CTAB) is shown to provid
16 ation of the DNA extraction method, in which cetyltrimethylammonium bromide (CTAB) is used to extract
17 hods, including Tris-EDTA Method, a modified Cetyltrimethylammonium Bromide (CTAB) Method, Alkaline M
18 a pi-helical conformation when stabilized by cetyltrimethylammonium bromide (CTAB) micelles and Zn(2+
19 To illustrate this concept, self-assembled cetyltrimethylammonium bromide (CTAB) molecules are used
20 procedures are the Surmodics procedure, the cetyltrimethylammonium bromide (CTAB) procedure, and the
22 talytic system using the cationic surfactant cetyltrimethylammonium bromide (CTAB) under UV irradiati
24 le a direct comparison, the same surfactant (cetyltrimethylammonium bromide (CTAB)) was used in each
25 precursor solution; however, the addition of cetyltrimethylammonium bromide (CTAB), a surfactant, ind
26 as exposed to aqueous solutions of cationic, cetyltrimethylammonium bromide (CTAB), and anionic, sodi
27 e surfactants, sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (CTAB), and polyoxyethyle
28 ries are achieved using their metal halides, cetyltrimethylammonium bromide (CTAB), and thiourea (Tu)
29 ueous solutions of NiMP-11 in the absence of cetyltrimethylammonium bromide (CTAB), NiMP-11 is aggreg
30 aptamers adsorbed via a cationic surfactant, cetyltrimethylammonium bromide (CTAB), on the LC surface
31 controlled using micelles of the surfactants cetyltrimethylammonium bromide (CTAB), or hexadecylamine
32 When the heme is encapsulated in micelles of cetyltrimethylammonium bromide (CTAB), photolysis of FeP
36 (SPCE) (ERGO/SPCE) coupled with ion-pairing (cetyltrimethylammonium bromide, CTAB) for the determinat
37 osuccinate (NaAOT) or the positively charged cetyltrimethylammonium bromide (CTABr), are analyzed wit
38 thylammonium bromide or SDS-acetic acid-urea-cetyltrimethylammonium bromide gels after exposure of ce
40 etic acid-urea-Triton X-100-acetic acid-urea-cetyltrimethylammonium bromide or SDS-acetic acid-urea-c
41 rile mixture and 1% concentrations of either cetyltrimethylammonium bromide or several polyoxyethylen
42 protocols: the in-house methods of CTAB-PVP (cetyltrimethylammonium bromide-polyvinylpyrrolidone), Wi
44 Detection was mediated by using synthesized cetyltrimethylammonium bromide-stabilized gold nanoparti
46 This new method involves the exchange of cetyltrimethylammonium bromide surfactants for an interm
47 structure-directing agent is the surfactant cetyltrimethylammonium bromide, the structure is 2-D hex
48 an be accomplished using a segment of dilute cetyltrimethylammonium bromide, which serves to temporar