ライフサイエンスコーパス: octyl glucoside

1 alpha(i-2) also resist extraction with 0.1 m octyl glucoside.

2 and extraction of the washed membranes with octyl glucoside.

3 ods is activation with detergents, such as n-octyl glucoside.

4 v Victory) root PM in an active form with 1% octyl-glucoside.

5 EYPC/cholate = 1.2 in 0.15 M NaCl, and EYPC/octyl glucoside = 0.13 in 0.15 M NaCl all form highly ov

6 One of them is 0.5% n-octyl glucoside/0.5% trifluoroacetic acid.

7 The addition of mannose 6-phosphate or octyl glucoside, a nonionic detergent containing a sugar

8 polipoprotein A-II and its complex with beta-octyl glucoside, a widely used lipid surrogate.

9 Octyl glucoside accelerated the dissociation rate by 3-5

10 At pH 8.5 in the presence of octyl glucoside and Ca2+ both forms exhibited a broad co

11 oluble in solutions containing the detergent octyl glucoside and formed high molecular mass oligomers

12 omal lysoplasmalogenase was solubilized with octyl glucoside and purified 500-fold to near homogeneit

13 nd both nonionic and ionic amphiphilic CPEs (octyl glucoside and sodium lauryl sulfate, respectively)

14 Their segregation between octyl glucoside and the detergent and aqueous phases of

15 detergents, n-octyl beta-D-glucopyranoside (octyl glucoside) and Triton X-100R-PC (Triton).

16 UCP1 was folded in octyl glucoside, as indicated by its high helical conten

17 to micelles composed of the detergents beta-octyl-glucoside (BOG) and SDS.

18 at obtained by using lytic concentrations of octyl glucoside but more sensitive to inhibition by cell

19 maleimide, the samples were solubilized with octyl glucoside/cholate and the subunit a was purified v

20 bserved a significantly lower Delta(1-43)A-I/octyl-glucoside complex partial specific volume than tha

21 e tested a range of detergents as follows: n-octyl glucoside, dodecyl maltoside, Triton X-100, Tween

22 , other detergents such as polydocanol, W-1, octyl glucoside, dodecyl maltoside, Tween 20, and sodium

23 inhibited by Nonidet P-40, Triton X-100, or octyl glucoside, even at concentrations up to 0.3%.

24 Here, octyl glucoside extraction of cells was used to identify

25 AO B was performed using protein prepared by octyl glucoside extraction.

26 -disc" model for bile salt-EYPC micelles and octyl glucoside-EYPC micelles principally because the nu

27 bacillus subsp. M3 were extracted with 1.25% octyl glucoside in the presence of 0.4% Escherichia coli

28 During BAX activation with n-octyl glucoside, it has been shown that BAX forms high m

29 In either octyl glucoside/lipid or dodecylmaltoside/lipid micelles

30 d-free receptor, solubilized in thermostable octyl glucoside micelles, exhibited a cooperative transi

31 sed in Escherichia coli and refolded in beta-octyl glucoside micelles.

32 ic changes, observed in the presence of beta-octyl glucoside, might provide clues to the structural b

33 concentration (1,2-dioleoyl-sn-glycerol) in octyl glucoside mixed micelles when the surface substrat

34 A single beta-octyl glucoside molecule outlines a possible receptor bi

35 ains (DIGs)/ caveolae, were solubilized by n-octyl glucoside (NOG, 1%) at 4 degrees C, and contained

36 Triton X-100, Triton X-114, NP-40, Brij-35, octyl glucoside, octyl thioglucoside, and lauryl maltosi

37 sulfhydryl-specific spin label, purified in octyl glucoside (OG), and reconstituted into palmitoylol

38 ubilized in sodium dodecyl sulfate (SDS) and octyl glucoside (OG), respectively.

39 aced with nondissociating detergents such as octyl glucoside or cholic acid.

40 hange when dodecyl maltoside was replaced by octyl glucoside or octyl glucoside-phospholipid-mixed mi

41 old increases barbed end nucleation sites in octyl glucoside-permeabilized platelets by 3-fold, enabl

42 maltoside was replaced by octyl glucoside or octyl glucoside-phospholipid-mixed micelles.

43 In Triton and octyl glucoside, plots of specific activity versus molec

44 Bacillus subtilis QST713, and the detergent octyl glucoside, respectively, with the detergent C12EO8

45 Typical detergents such as C(12)EO(8), octyl glucoside, SDS, and lauryl maltoside initiate memb

46 analyses showed that the oligomeric state of octyl glucoside-solubilized GlpF varies: low ionic stren

47 GLUT1 forms a multimeric complex in octyl glucoside that dissociates upon addition of reduct

48 Isolated from human blood platelets in octyl glucoside, the alphaIIbbeta3 complex behaved as an

49 dized glutathione and the nonionic detergent octyl glucoside, the G protein regained considerable nat

50 toskeletal proteins, though its retention in octyl-glucoside-treated platelets and ultrastructural ob

51 of this epitope was observed in W-1, Chaps, octyl glucoside, Tween 20, and Brij 35.

52 retinae by immunoaffinity chromatography in octyl glucoside was reconstituted into liposomes prepare

53 differential effects of detergents (CHAPS vs octyl glucoside), we have shown that this direct interac

54 ivatives) and the glycoacyl chain detergent, octyl glucoside, with egg yolk phosphatidylcholine (EYPC