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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 les and to the unconventional aggregation of sodium cholate.
8 e DDT in the presence of solubilizing factor sodium cholate.
9 glucoside, dodecyl maltoside, Tween 20, and sodium cholate allow varying degrees of Bax hetero- and
10 f total human plasma lipoproteins (TLP) with sodium cholate and its subsequent removal, has been used
13 n X-114, polydocanol, dodecyl maltoside, and sodium cholate, and no exposure of this epitope was obse
14 ng two different detergents, RapiGest SP and sodium cholate, and two different trypsins, sequencing g
15 spersed in 20 mM phospholipid requires 50 mM sodium cholate, concentrations that are commonly used to
16 isolated through partial solubilization with sodium cholate detergent, and the partially purified rec
17 reconstituted HDL particles prepared by the sodium cholate dialysis method, has shown that mutants (
18 nicating single-walled carbon nanotubes with sodium cholate, followed by surfactant exchange to form
19 taining 15% fat, 1.25% cholesterol, and 0.5% sodium cholate for 12 weeks, and atherosclerotic lesions
23 and 1.25% cholesterol supplemented with 0.5% sodium cholate) or given methotrexate intraperitoneally.
24 tructure of sodium dodecyl sulfate (SDS) and sodium cholate (SC) in aqueous solutions with and withou
25 Conversely, dimerization of CcO induced by sodium cholate significantly increases its kinetic stabi
28 n of SWCNTs coated with various surfactants (sodium cholate, sodium dodecyl sulfate, and cetyl trimet
31 s, as well as those determined for benchmark sodium cholate suspensions of (6,5) SWNTs, are similar;
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