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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
9                                          The microcolumn allows one to preconcentrate up to 100 mL of
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
14                       We describe a reusable microcolumn and process for the efficient discovery of n
15 en the sample and an anti-BSA immunoaffinity microcolumn and provided a signal within 5-25 s after sa
16  (CPG) with a bonded phase that is used with microcolumns and a flow injection analysis system.
17 n the spatial distribution of the neurons in microcolumns and/or neuronal loss.
18                                The described microcolumns are applicable to high-pressure analytical
19                          Silica-based lectin microcolumns are described in this study together with t
20                        Laser-induced silicon microcolumn arrays (LISMA) were developed as matrix-free
21 DI-MS experiments with a nitrogen laser, the microcolumn arrays obtained in water environment readily
22                               In turn, these microcolumn arrays were used as matrix-free soft laser d
23  19 different targets simultaneously using a microcolumn-based device, MEDUSA (Microplate-based Enric
24                   It was concluded that TiO2 microcolumns can be used to enrich aged OP-modified BChE
25              Active sites in a silicon-Pyrex microcolumn cause peak tailing and unwanted adsorption.
26 were obtained on the coated partially buried microcolumn compared to 0.66 mm and 6.73, respectively,
27 orm phase deposition in the partially buried microcolumn compared to the square DRIE microcolumn.
28 r elution of n-C(12) on the partially buried microcolumn compared to the square DRIE microcolumn.
29 entrated in-line before the detector using a microcolumn containing 10 mg of imprinted BENZ or DEB.
30 n was extracted in approximately 100 ms by a microcolumn containing a small layer of anti-phenytoin a
31                                            A microcolumn containing an Affi-Gel resin derivatized wit
32                         First, we designed a microcolumn containing recombinant Protein L that was im
33               It was found that the affinity microcolumns could be used in either frontal analysis or
34 he linkage of wing cracks or the buckling of microcolumns created between adjacent wing cracks.
35 ng to the bending-induced failure of slender microcolumns created between sets of secondary cracks em
36 ized the selection process performance using microcolumns filled with green fluorescent protein (GFP)
37 nt of a new temperature-controlled renewable microcolumn flow cell for solid-phase nucleic acid hybri
38 zyme and enable it to be packed into a model microcolumn for application as a biosensor or as a biore
39  as an immobilized binding agent in affinity microcolumns for the analysis of free drug fractions.
40 ates how to prepare microfabricated columns (microcolumns) for organophosphonate and organosulfur com
41 pared muMNPCs are exploited as sorbents in a microcolumn format in a sequential injection analysis (S
42                                          The microcolumns had good stability and allowed data to be o
43                  Anatomical changes to these microcolumns have been correlated with neurological dise
44 ther oxidative and methylated metabolites by microcolumn high-performance liquid chromatography with
45 nt mix was separated on the partially buried microcolumn in 3.8 s with the maximum peak width at half
46 nd temperature conditions on the square DRIE microcolumn in 4.6 s.
47 d collective and reproducible fabrication of microcolumns in a silicon wafer.
48 from condensed-matter physics, we quantified microcolumns in area 46 of seven young and seven aged rh
49 ally significant decrease in the strength of microcolumns, indicating microcolumnar disorganization.
50 em through the use of an extra CaCO3-PEI MPs microcolumn is achieved.
51 henyl boronate affinity preconcentration and microcolumn liquid chromatography, followed by mass spec
52                       With the use of packed microcolumns (<0.5 mm i.d.), essentially instantaneous h
53 e better performance of the partially buried microcolumn may be attributed to either the rounded chan
54 e deactivation lowers adsorption activity in microcolumns more than silazane and silane treatments.
55          A flow injection (FI) system with a microcolumn of anion exchanger has been used to effect r
56                                              Microcolumns of hydrophobic beads packed against the pol
57                                              Microcolumns of staphylococcal protein A linked to Sepha
58 ation of lead and strontium by sorption on a microcolumn packed with Sr-resin using an inductively co
59 er mammals organize themselves into vertical microcolumns perpendicular to the pial surface.
60 ent of the solid bed of particles inside the microcolumn, preventing their aggregation, increasing th
61 inetic and equilibrium data obtained for the microcolumns, quantitative analysis can be done prior to
62  design, assessment, and utility of affinity microcolumn sensors.
63  interface permitted the on-line coupling of microcolumn separation techniques with MALDI MS, as demo
64 xtracted in 180 ms by a 2.1-mm-i.d. sandwich microcolumn that contained a 1.1-mm layer of an anti-war
65 apture of free phenytoin by immunoextraction microcolumns, the behavior of NIR fluorescent labels in
66 e stacked on a C18 reversed-phase extraction microcolumn, thus enriching and cleaning up the analytes
67 ly lost from samples desalted by ZipTip(C18) microcolumns, thus diminishing the quality of the finger
68 sign between parallel and serially-connected microcolumns to enable the use of just 2 aliquots of sta
69   This report used high-performance affinity microcolumns to examine the changes in binding by sulfon
70 ied microcolumns, which had a unique rounded microcolumn wall profile similar to that of a flattened
71                         The partially buried microcolumn was found to perform closer to the theoretic
72               A similarly designed Protein G microcolumn was utilized to first perform an online depl
73                         Versatility of these microcolumns was demonstrated with a high-temperature C1
74  of the rhesus monkey brain, the strength of microcolumns was shown to decrease with age.
75 ure-programmed silica- or graphite-sputtered microcolumns were investigated: a separation of light al
76          Following initial tests, the lectin microcolumns were utilized for enrichment of glycoprotei
77 umn and two-dimensional systems based on HSA microcolumns were utilized to measure the free fraction
78 cm long, 100 microm x 100 microm square DRIE microcolumn, which had a similar hydraulic diameter.
79 om wide, and 65 microm deep partially buried microcolumns, which had a unique rounded microcolumn wal
80 ed reduction in total neuronal density or in microcolumn width, length, or periodicity.
81 s were generated with a 3 m long OV-5-coated microcolumn with a 0.25 microm phase thickness using hel
82 .73, respectively, on the coated square DRIE microcolumn with a similar retention factor.
83                       The combination of our microcolumns with a multiplex approach and high-throughp
84 amples desalted by ZipTip(C18) reverse-phase microcolumns with on-plate washing of peptides deposited
85 ctivation procedures appropriate for silicon microcolumns with Pyrex tops.

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