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1 10(4) were obtained in the SDS micro-CGE and MEKC separation dimensions, respectively, for the invest
2 to provide a complementary method to CZE and MEKC for the separation of specific types of solutes tha
3 y IR and NMR spectroscopies, whereas CZE and MEKC were applied to evaluate their purity and to invest
4 nic chiral polymeric surfactants in MEKC and MEKC-MS.
5  sources of congeneric relationships between MEKC retention and log Po/w.
6 astereomers of some of them, was achieved by MEKC in an acidic BGE (500 mM acetic acid [pH 2.54] and
7 kaline background electrolytes (BGEs) and by MEKC in acidic and alkaline BGEs containing a pseudostat
8 ounds in the training set were determined by MEKC, while the K(mw) of the aliphatic solutes were esti
9 bicide spiked in lake water was separated by MEKC and detected by ultraviolet absorption.
10 ly labeled substrates followed by an on-chip MEKC separation of the reaction products from the substr
11 lar electrokinetic capillary chromatography (MEKC) and the high sensitivity of fluorescence detection
12 lar electrokinetic capillary chromatography (MEKC).
13 s in micellar electrokinetic chromatography (MEKC) can be improved significantly.
14 e of micellar electrokinetic chromatography (MEKC) coupled to inductively coupled plasma-mass spectro
15 , in micellar electrokinetic chromatography (MEKC) is directly related to solute partition coefficien
16  and micellar electrokinetic chromatography (MEKC) is discussed here.
17 sive micellar electrokinetic chromatography (MEKC) method with UV detection was used to determine sev
18 wing micellar electrokinetic chromatography (MEKC) separations in a 19.6-cm-long serpentine channel,
19 r 74 micellar electrokinetic chromatography (MEKC) systems taken from the literature.
20 sing Micellar Electrokinetic Chromatography (MEKC) to estimate the octanol-water partition coefficien
21 e to micellar electrokinetic chromatography (MEKC) to monitor extracellular dopamine concentration in
22 , in micellar electrokinetic chromatography (MEKC) using the simple relationship k = K(mw)phi, where
23  and micellar electrokinetic chromatography (MEKC) were used as the separation modes for the first an
24      Micellar electrokinetic chromatography (MEKC) which separates PB-labeled amino acids by their hy
25 ling micellar electrokinetic chromatography (MEKC) with electrospray mass spectrometry initiates the
26  and micellar electrokinetic chromatography (MEKC) with laser-induced fluorescence detection was expl
27  and micellar electrokinetic chromatography (MEKC), containing sodium dodecyl sulfate, applies the pr
28 s by micellar electrokinetic chromatography (MEKC), two-dimensional correlation analysis resolved all
29 ) in micellar electrokinetic chromatography (MEKC).
30 with micellar electrokinetic chromatography (MEKC).
31 s in micellar electrokinetic chromatography (MEKC).
32 ) to micellar electrokinetic chromatography (MEKC).
33  and micellar electrokinetic chromatography (MEKC).
34 n by micellar electrokinetic chromatography (MEKC).
35 n by micellar electrokinetic chromatography (MEKC).
36  and flavonoids has been developed combining MEKC and DAD detection.
37              In comparison with conventional MEKC, only a small portion of the capillary is filled wi
38 y with laser-induced fluorescence detection (MEKC-LIF) making it possible to detect superoxide found
39 elution peaks unseparable by one-dimensional MEKC, demonstrating the utility of 2D correlation in sep
40 ecyl sulfate to the separation buffer (i.e., MEKC) resulted in peak splitting for all four serogroups
41 lications, and advantages of partial-filling MEKC are similarly addressed.
42 ons between conventional and partial-filling MEKC in terms of separation efficiency and resolution of
43 or of triazine herbicides in partial-filling MEKC.
44 initiates the development of partial-filling MEKC.
45 performing the separation in partial-filling MEKC.
46 te numbers of 230000 and 40000 in the first (MEKC) and second (CE) dimensions, respectively, correspo
47 c chromatography-laser induced fluorescence (MEKC-LIF) method was developed using sodium dodecylbenze
48 e electric field strengths were 200 V/cm for MEKC and 2400 V/cm for CE.
49  by a gated valve onto a separate column for MEKC analysis.
50                 The use of Ag(I) addition in MEKC is also applied to the separation of various other
51 e results using Ag(I) as buffer additives in MEKC are also compared to studies utilizing a mixed coun
52 a priori prediction of retention behavior in MEKC from solute structure.
53 ship for prediction of retention behavior in MEKC is examined.
54  the retention times (thus chromatograms) in MEKC can be predicted from the calculated retention fact
55  coefficient can be accurately determined in MEKC for a given micellar pseudostationary phase.
56          This means that retention factor in MEKC can be predicted for solutes with known micelle-wat
57                      Retention mechanisms in MEKC separations can also be manipulated by the addition
58 he addition of Ag(I) on the elution range in MEKC is also investigated.
59 ying anionic chiral polymeric surfactants in MEKC and MEKC-MS.
60  from the antibody and analyzed by microchip MEKC.
61 corporated a 30-mm SDS micro-CGE and a 10-mm MEKC dimension length.
62 ir of sulfonamides was achieved under normal MEKC conditions.
63                                   The use of MEKC as the separation mode significantly increased the
64                  After careful optimization, MEKC-ICP-MS was used to separate engineered nanoparticle
65                                The optimized MEKC conditions (45 mM CHAPSO, pH 6 at 5 degrees C) effe
66                     With the use of the PNAA-MEKC method, PCR products of 88, 134, 216, and 447 bases
67                                  A sensitive MEKC-mass spectrometry (MS) method is developed for one
68 able and remained fluorescent under standard MEKC conditions for peptide and protein separations.
69                                          The MEKC separation buffer consisted of 30 mM phosphate, 6.5
70 ion with the electrophoresis run time in the MEKC dimension being 10 s.
71                                        Using MEKC to separate the dialysate samples allowed aspartate
72 sal concentrations for these compounds using MEKC were 1.9 +/- 0.2, 4.1 +/- 0.2, 4.6 +/- 0.7, 2.6 +/-
73  conductivity detection were performed using MEKC, in which the carrier electrolyte contained the ani
74                                      Various MEKC background electrolyte (BGE) solutions were prepare

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