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1 s according to their pI values without using ampholytes.
2 rom ITP experiments with fluorescent carrier ampholytes.
3 l generated by impurities present within the ampholytes.
4 ct the human absolute bioavailability of the ampholytes.
5 tion limits were 310 +/- 30 zmol with pH 4-8 ampholytes.
6 icroclimate pH effects in the case of acidic ampholytes.
7 al generated by impurities within commercial ampholytes.
8 conditions, without the addition of carrier ampholytes.
9 ocusing (cIEF) using a set of amino acids as ampholytes.
10 ) in the detection of nonfluorescing carrier ampholytes.
11 ctric points (pI) without the use of carrier ampholytes.
12 er ITP and displace subsets of these carrier ampholytes.
13 tions including high levels of contaminating ampholytes and complex fractionation and isolation proce
14 f the chamber, we used free solution carrier ampholytes and immobilized acrylamido buffers in the PA
15 label a mixture of low-concentration carrier ampholytes and introduce it into an isotachophoresis (IT
17 eins in a straight channel using broad-range ampholytes and then refocusing segments of the first cha
18 d on the charge to mass without resorting to ampholytes and/or isoelectric focusing, using a single-
20 nstrated with little or no interference from ampholyte, and CIEF-RPLC-MS data are used to construct a
21 itive interference with the aminoglycosides, ampholytes, and phenothiazines and negative interference
23 e by 2 cm long in 3-10 min using broad-range ampholytes at electric field strengths ranging from 25 t
24 ed-silica capillary in a solution of carrier ampholytes at physiological pH and osmolarity, where the
28 rated using bovine serum albumin in a single ampholyte buffer as well as in multiple-component buffer
30 increases essentially in presence of carrier ampholyte (CA) components, which makes problematic a rel
31 showed that the ITP displacement of carrier ampholytes can be used for detection of unlabeled (nonfl
32 assays to interference from aminoglycosides, ampholytes, detergents, phenothiazines, reducing agents,
33 rves relating effective mobility and carrier ampholyte displacement at two different leading electrol
34 rge number (on the order of 1000) of carrier ampholytes enables detection of a wide range of analytes
35 an overcome these problems but is limited by ampholyte interference and signal quenching in ESI-MS.
36 shown to be separated using a linear carrier ampholyte (linear pH gradient between two electrodes) of
38 ocusing performed with photobleached pH 3-10 ampholytes produced concentration detection limits of 27
42 the addition of a small pI range (4-6.5) of ampholytes to improve resolution and stability of the co
43 m charge arising from covalent attachment of ampholytes to the benzophenone-functionalized gel matrix
45 an accurate measure of the amount of carrier ampholytes which are focused between the leading electro
46 o 10 microL/min and does not require carrier ampholytes, which can create molecular backgrounds for s
47 h the exception of two compounds, all of the ampholytes with bioavailability <50% were predominantly
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