ライフサイエンスコーパス: Tween 20

1 ta-lactoglobulin) or a non-ionic surfactant (Tween 20).

2 le to colour fading than those stabilized by Tween 20.

3 eased when the enzyme assays contained 0.02% Tween 20.

4 molecular-weight oligomers are stabilized by Tween 20.

5 formulations containing sucrose, salts, and Tween 20.

6 the growth of 8830R2::Cm in the presence of Tween 20.

7 n X-100 (RTX-100), octylglucopyranoside, and Tween 20.

8 led these strains to grow in the presence of Tween 20.

9 nt of black currants with 0.02mM MJ in 0.05% Tween-20.

10 wells; unbound AFP was then washed away with Tween-20.

11 ly, when the assay buffer contains traces of Tween 20 (0.0001%), darbufelone appears inactive with PG

12 sence of low concentrations of the detergent Tween 20 (0.05-0.1%, v/v) in the wash buffer as well as

13 dentified an optimized formulation of 1% w/v Tween-20, 0.8 ug/uL bovine serum albumin, 1 M betaine in

14 glucoside, dodecyl maltoside, Triton X-100, Tween 20, 3-[(3-cholamidopropyl)dimethylammonio]-1-propa

15 For steric emulsifiers, Tween 20, 40, 60 and 80 were used to produce nanodispers

16 factant-to-oil ratio (SOR), surfactant type (Tween 20, 40, 60, 80 and 85), and stirring conditions on

17 d to study the influence of surfactant type (Tween 20, 60 and 80) and oil type (Vitamin E, vitamin D(

18 a major impact of non-ionic surfactant type (Tween 20, 60 or 80) on the formation and properties of t

19 in their ability to grow in the presence of Tween 20, a detergent that inhibits a kinase which can s

20 ied starch and whey protein isolate, but not Tween 20, affected the cell viability/proliferation more

21 1 hour) and chemical inactivation with 0.5% Tween-20 against a high titer of Ebola virus (species Za

22 The Tween 20 allowed lower detection limits to be obtained f

23 formulations with aqueous solutions of 0.03% Tween 20 altered the time of dissolution for all cases.

24 m the Schirmer strip in 0.5 M NaCl with 0.5% Tween 20 and analyzed using multiplex assay kits to exam

25 pted by exposure to mild neutral detergents (Tween 20 and CHAPS) at concentrations from 0.25 to 2.0%.

26 mines the potential of two buffer additives (Tween 20 and DTT) to improve the solubility of proteins

27 elicited as 30 mg of cholesterol, 150 mg of Tween 20 and feeding time of 1 min at a stirring rate of

28 formation is inhibited by concentrations of Tween 20 and several other detergents well below their c

29 promising ratio between the two surfactants, Tween 20 and Span 60, in terms of entrapment efficiency

30 nanoemulsions emulsified by modified starch, Tween 20 and whey protein isolate, respectively, were pr

31 Three types of emulsifiers, lecithin, Tween-20 and sodium dodecyl sulphate (SDS) were tested.

32 a, Polyethylene glycol sorbitan monolaurate (Tween 20) and Cetylpyridinium chloride (CPC) in Tris/HCl

33 e buffer (pH 8.8 containing 1% BSA and 0.05% Tween 20) and pipetted onto the sample-cum-conjugate pad

34 was observed in W-1, Chaps, octyl glucoside, Tween 20, and Brij 35.

35 tion was inhibited by the nonionic detergent Tween 20, and several lipids did not enhance enzymatic a

36 ol, W-1, octyl glucoside, dodecyl maltoside, Tween 20, and sodium cholate allow varying degrees of Ba

37 on of nonionic surfactants (Triton X-100 and Tween 20) arrays from the second series exhibit signific

38 m) were formed using a non-ionic surfactant (Tween 20) as emulsifier and long chain triglycerides (LC

39 hed three times, then solubilized with 0.04% Tween 20 at a detergent/protein (w/w) ratio of 0.1.

40 A tween 20 coating method is developed to inhibit non-spec

41 gents such as Triton X-100, Nonidet P-40 and Tween 20 did not affect the activities, while anionic de

42 mass spectrometric analyses, the presence of Tween-20 did not prevent detection of ricin peptides, an

43 In contrast, formulations containing Tween 20 dissolved faster in the Tween 20 solution when

44 Salt and sucrose formulations without Tween 20 dissolved more slowly in a Tween 20 solution th

45 method based on dichlorodimethylsilane (DDS)-Tween-20 for in vitro single-molecule studies, which, un

46 ed assays performed in buffers that included Tween-20 gave better results than assays performed using

47 rol (0.5% carboxymethyl cellulose and 0.025% Tween 20 in distilled water) or 750 mg silibinin/kg body

48 affect darbufelone in this way, in place of Tween 20 in our PGHS buffers.

49 containing 0.5% methyl cellulose and 0.025% Tween 20 in two different protocols.

50 were prepared from mixtures of olive oil and Tween 20 in water.

51 ates, in emulsions prepared with lecithin or Tween-20, indicating the greater relevance of having thr

52 Tween-20 ligand showed the best binding affinity by hydr

53 ic acid and autoxidation of linoleic acid in Tween 20 micellar medium) and compared with three widely

54 However, Tween 20 micelles did appear to be able to solubilise le

55 E(8), followed by exchange of C(12)E(8) with Tween 20 on a Superose 6 column.

56 sein, whey protein) and surfactants (Citrem, Tween 20) on the in vitro digestion and oxidation of lin

57 thesis could be abolished by the addition of Tween 20 or Triton X-100.

58 ions, from the nonionic class (Triton X-100, Tween 20) or from the zwitterionic class (3-[(3-cholamid

59 Moreover, the influence of Tween 20 over the analytical parameters was studied.

60 r and StartingBlock phosphate buffer saline- Tween-20; (PBS-T20) blocking buffer was utilized to mini

61 e substrate in 50 mM NaOAc, 150 mM KF, 0.05% Tween 20, pH 5.5, with apparent first-order kinetics wit

62 which neutral additives (e.g., Triton X-100, Tween 20, poly(ethylene glycol)) are removed from protei

63 Dilution experiments of cinaciguat/Tween 20-preincubated sGC revealed the irreversible char

64 The emulsion produced with Tween 20 resisted coalescence in the gastric phase and s

65 nd poorly to MTP, but its preincubation with Tween-20 resulted in significantly increased binding to

66 riments with purified sGC in the presence of Tween 20 showed that cinaciguat activates the heme-free

67 Other detergents, e.g., Tween 20, sodium cholate, sodium deoxycholate, CHAPS, or

68 y bound cardiolipin (CL) can be removed from Tween 20 solubilized bovine cytochrome bc(1) (EC 1.10.2.

69 Phospholipid removal from the Tween 20 solubilized enzyme, including the tightly bound

70 without Tween 20 dissolved more slowly in a Tween 20 solution than in water alone.

71 containing Tween 20 dissolved faster in the Tween 20 solution when compared to dissolution in water.

72 ctoglobulin-stabilised nanoemulsions than in Tween 20-stabilised ones.

73 Tween 20 stabilized corn O/W emulsions at pH 7.0 were pr

74 e and lauryl gallate in the aqueous phase of Tween 20-stabilized and CTAB-stabilized emulsions, respe

75 rson correlation coefficients showed that in Tween 20-stabilized emulsions, aqueous lauryl gallate, i

76 d autoxidation within single oil droplets in Tween-20-stabilized oil-in-water emulsion was achieved b

77 Lastly, Tween 20 substantially and selectively increases NTPDase

78 The DDS-Tween-20 surface was simple and inexpensive to prepare a

79 In contrast, for emulsions prepared with Tween-20, the antioxidants seem to follow the polar para

80 a Tris-HCl buffer containing the surfactant Tween 20 to aid in the prevention of surface adhesion of

81 ngth of the desalted serum and also utilized Tween 20 to serve as the passivation agent by surface mo

82 ey protein concentrate hydrolysate (WPCH) or Tween 20 (TW20) were used as the emulsifiers.

83 ution (1.5% carboxymethylcellulose with 0.2% Tween 20) via gastrointestinal gavage.

84 PBS that contains 1 M NaCl and 2% Tween 20 was determined to be the optimal extraction buf

85 PBS that contains 1 M NaCl and 2% Tween 20 was determined to be the optimal extraction buf

86 The detergent polysorbate 20 (Tween 20) was used successfully to facilitate the remova

87 ulsions consisting of water, tricaprylin and Tween 20 were prepared, thermally treated and the format

88 fish oil-in-water emulsions stabilized with Tween 20, where emulsion physical stability was unaffect