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1 -12 nmol of protein to prepare each affinity microcolumn.
2 ried microcolumn compared to the square DRIE microcolumn.
3 zone electrophoresis (GEITP-CZE) in a single microcolumn.
4 ried microcolumn compared to the square DRIE microcolumn.
5 tion of the analyte on an 8-hydroxyquinoline microcolumn.
6 s of neurons across all layers of a cortical microcolumn.
7 droxyquinolinol immobilized on CPG packed in microcolumns.
8 is the vertical arrangement of neurons into microcolumns, a fundamental computational unit of the co
10 nt gradient delivery module, a reverse phase microcolumn and an electrospray ionization ion trap mass
11 odeling of kinetic responses of the affinity microcolumn and are consistent with those obtained by fl
12 tion of IL phase were achieved with a packed microcolumn and As(III) was determined in eluent solutio
13 ated using breakthrough curves from a packed microcolumn and flame atomic absorption spectrophotometr
15 en the sample and an anti-BSA immunoaffinity microcolumn and provided a signal within 5-25 s after sa
21 DI-MS experiments with a nitrogen laser, the microcolumn arrays obtained in water environment readily
24 19 different targets simultaneously using a microcolumn-based device, MEDUSA (Microplate-based Enric
27 LA printing was used to produce 360 mum I.D. microcolumn chips with excellent structural properties.
28 were obtained on the coated partially buried microcolumn compared to 0.66 mm and 6.73, respectively,
29 orm phase deposition in the partially buried microcolumn compared to the square DRIE microcolumn.
30 r elution of n-C(12) on the partially buried microcolumn compared to the square DRIE microcolumn.
31 entrated in-line before the detector using a microcolumn containing 10 mg of imprinted BENZ or DEB.
32 n was extracted in approximately 100 ms by a microcolumn containing a small layer of anti-phenytoin a
37 ng to the bending-induced failure of slender microcolumns created between sets of secondary cracks em
38 uid chromatography-MS/MS setup, the protease microcolumn enabled reproducible protein digestion and p
39 ized the selection process performance using microcolumns filled with green fluorescent protein (GFP)
40 nt of a new temperature-controlled renewable microcolumn flow cell for solid-phase nucleic acid hybri
41 zyme and enable it to be packed into a model microcolumn for application as a biosensor or as a biore
42 as an immobilized binding agent in affinity microcolumns for the analysis of free drug fractions.
43 ates how to prepare microfabricated columns (microcolumns) for organophosphonate and organosulfur com
44 pared muMNPCs are exploited as sorbents in a microcolumn format in a sequential injection analysis (S
47 ther oxidative and methylated metabolites by microcolumn high-performance liquid chromatography with
48 nt mix was separated on the partially buried microcolumn in 3.8 s with the maximum peak width at half
51 from condensed-matter physics, we quantified microcolumns in area 46 of seven young and seven aged rh
52 ally significant decrease in the strength of microcolumns, indicating microcolumnar disorganization.
54 henyl boronate affinity preconcentration and microcolumn liquid chromatography, followed by mass spec
56 e better performance of the partially buried microcolumn may be attributed to either the rounded chan
57 e deactivation lowers adsorption activity in microcolumns more than silazane and silane treatments.
61 ation of lead and strontium by sorption on a microcolumn packed with Sr-resin using an inductively co
63 ent of the solid bed of particles inside the microcolumn, preventing their aggregation, increasing th
64 inetic and equilibrium data obtained for the microcolumns, quantitative analysis can be done prior to
66 interface permitted the on-line coupling of microcolumn separation techniques with MALDI MS, as demo
67 xtracted in 180 ms by a 2.1-mm-i.d. sandwich microcolumn that contained a 1.1-mm layer of an anti-war
68 ase solid-phase extraction (Oasis PRIME-HLB) microcolumn that is captured into the channels of an LOV
69 apture of free phenytoin by immunoextraction microcolumns, the behavior of NIR fluorescent labels in
70 e stacked on a C18 reversed-phase extraction microcolumn, thus enriching and cleaning up the analytes
71 ly lost from samples desalted by ZipTip(C18) microcolumns, thus diminishing the quality of the finger
72 sign between parallel and serially-connected microcolumns to enable the use of just 2 aliquots of sta
73 This report used high-performance affinity microcolumns to examine the changes in binding by sulfon
74 ied microcolumns, which had a unique rounded microcolumn wall profile similar to that of a flattened
79 ure-programmed silica- or graphite-sputtered microcolumns were investigated: a separation of light al
81 umn and two-dimensional systems based on HSA microcolumns were utilized to measure the free fraction
82 cm long, 100 microm x 100 microm square DRIE microcolumn, which had a similar hydraulic diameter.
83 om wide, and 65 microm deep partially buried microcolumns, which had a unique rounded microcolumn wal
85 s were generated with a 3 m long OV-5-coated microcolumn with a 0.25 microm phase thickness using hel
87 for VOC capture and injection; a wall-coated microcolumn with thin-metal heaters and temperature sens
89 amples desalted by ZipTip(C18) reverse-phase microcolumns with on-plate washing of peptides deposited