ライフサイエンスコーパス: cetyltrimethylammonium bromide

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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.

5 water-in-oil microemulsion droplets made of cetyltrimethylammonium bromide/1-butanol/isooctane.

6 Both solutions contain cetyltrimethylammonium bromide and sodium salicylate.

7 ve template system, comprising a surfactant (cetyltrimethylammonium bromide) and a chelating agent (c

8 ns were conducted with a catalytic amount of cetyltrimethylammonium bromide as phase-transfer agent a

9 luminum isopropoxide as aluminum source, and cetyltrimethylammonium bromide as template.

10 Using CTAB (cetyltrimethylammonium bromide) as the structure-directi

11 d a borate-phosphate buffer containing 25 mM cetyltrimethylammonium bromide (CTAB) at pH 9.50 was use

12 obic ternary complexes formed in presence of cetyltrimethylammonium bromide (CTAB) into a 125muL volu

13 sis in combination with dynamic coating with cetyltrimethylammonium bromide (CTAB) is shown to provid

14 ation of the DNA extraction method, in which cetyltrimethylammonium bromide (CTAB) is used to extract

15 hods, including Tris-EDTA Method, a modified Cetyltrimethylammonium Bromide (CTAB) Method, Alkaline M

16 a pi-helical conformation when stabilized by cetyltrimethylammonium bromide (CTAB) micelles and Zn(2+

17 To illustrate this concept, self-assembled cetyltrimethylammonium bromide (CTAB) molecules are used

18 procedures are the Surmodics procedure, the cetyltrimethylammonium bromide (CTAB) procedure, and the

19 ating, which was prepared in the presence of cetyltrimethylammonium bromide (CTAB) surfactant.

20 le a direct comparison, the same surfactant (cetyltrimethylammonium bromide (CTAB)) was used in each

21 as exposed to aqueous solutions of cationic, cetyltrimethylammonium bromide (CTAB), and anionic, sodi

22 ries are achieved using their metal halides, cetyltrimethylammonium bromide (CTAB), and thiourea (Tu)

23 ueous solutions of NiMP-11 in the absence of cetyltrimethylammonium bromide (CTAB), NiMP-11 is aggreg

24 controlled using micelles of the surfactants cetyltrimethylammonium bromide (CTAB), or hexadecylamine

25 When the heme is encapsulated in micelles of cetyltrimethylammonium bromide (CTAB), photolysis of FeP

26 es in an aqueous solution in the presence of cetyltrimethylammonium bromide (CTAB).

27 dodecyl sulfate (SDS) or cationic detergent cetyltrimethylammonium bromide (CTAB).

28 For cetyltrimethylammonium bromide (CTAB)/sodium octyl sulfo

29 thylammonium bromide or SDS-acetic acid-urea-cetyltrimethylammonium bromide gels after exposure of ce

30 the combination of hydroxide base, H2O, and cetyltrimethylammonium bromide in toluene solvent.

31 etic acid-urea-Triton X-100-acetic acid-urea-cetyltrimethylammonium bromide or SDS-acetic acid-urea-c

32 rile mixture and 1% concentrations of either cetyltrimethylammonium bromide or several polyoxyethylen

33 protocols: the in-house methods of CTAB-PVP (cetyltrimethylammonium bromide-polyvinylpyrrolidone), Wi

34 ged micelles from sodium dodecyl sulfate and cetyltrimethylammonium bromide, respectively.

35 Addition of a cetyltrimethylammonium bromide surfactant to the separat

36 This new method involves the exchange of cetyltrimethylammonium bromide surfactants for an interm

37 structure-directing agent is the surfactant cetyltrimethylammonium bromide, the structure is 2-D hex

38 an be accomplished using a segment of dilute cetyltrimethylammonium bromide, which serves to temporar

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