ライフサイエンスコーパス: sodium cholate

1 ation with Bio-Beads SM-2 in the presence of sodium cholate.

2 etastable HDL and LDL to mixed micelles with sodium cholate.

3 ent requires an equal molar concentration of sodium cholate.

4 cO will not reassociate upon the addition of sodium cholate.

5 anesulfonic acid, and a low concentration of sodium cholate.

6 solubilized equally from E2M11 membranes by sodium cholate.

7 analogs, cholesteryl hemisuccinate (CHS) and sodium cholate.

8 les and to the unconventional aggregation of sodium cholate.

9 e DDT in the presence of solubilizing factor sodium cholate.

10 ion capacities for cholesterol (19.27 mg/g), sodium cholate (8.47 mg/g), and glucose.

11 glucoside, dodecyl maltoside, Tween 20, and sodium cholate allow varying degrees of Bax hetero- and

12 f total human plasma lipoproteins (TLP) with sodium cholate and its subsequent removal, has been used

13 Sodium cholate and taurocholate induced cytosolic Ca(2+)

14 erential centrifugation and solubilized with sodium cholate and urea.

15 n X-114, polydocanol, dodecyl maltoside, and sodium cholate, and no exposure of this epitope was obse

16 ng two different detergents, RapiGest SP and sodium cholate, and two different trypsins, sequencing g

17 spersed in 20 mM phospholipid requires 50 mM sodium cholate, concentrations that are commonly used to

18 isolated through partial solubilization with sodium cholate detergent, and the partially purified rec

19 reconstituted HDL particles prepared by the sodium cholate dialysis method, has shown that mutants (

20 nicating single-walled carbon nanotubes with sodium cholate, followed by surfactant exchange to form

21 taining 15% fat, 1.25% cholesterol, and 0.5% sodium cholate for 12 weeks, and atherosclerotic lesions

22 the beta(1)AR receptor was observed by DEER, sodium cholate induces specific beta(1)AR dimerization (

23 Sodium cholate is critical because it does not interfere

24 on in the anionic sodium dodecyl sulfate and sodium cholate micelle systems.

25 In the absence of surfactant (sodium cholate, NaC), multilayer graphene had higher ads

26 and 1.25% cholesterol supplemented with 0.5% sodium cholate) or given methotrexate intraperitoneally.

27 ation of spin-labeled beta(1)AR with CHS and sodium cholate reveal the following: CHS binds specifica

28 tructure of sodium dodecyl sulfate (SDS) and sodium cholate (SC) in aqueous solutions with and withou

29 SWCNTs as the internal either turn-off (with sodium cholate (SC)) or reference (with carboxymethylcel

30 Conversely, dimerization of CcO induced by sodium cholate significantly increases its kinetic stabi

31 Other detergents, e.g., Tween 20, sodium cholate, sodium deoxycholate, CHAPS, or CHAPSO, a

32 rizes upon the addition of bile salts, e.g., sodium cholate, sodium deoxycholate, or CHAPS.

33 n of SWCNTs coated with various surfactants (sodium cholate, sodium dodecyl sulfate, and cetyl trimet

34 In Triton X-100 and sodium cholate solutions, the aggregated, unfolded, and

35 In this study, we describe the use of a sodium cholate suspension-dialysis method to adsorb the

36 s, as well as those determined for benchmark sodium cholate suspensions of (6,5) SWNTs, are similar;

37 While no direct binding of sodium cholate to the beta(1)AR receptor was observed by