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1  ions and one-dimensional aggregation of the gold colloids.
2 d toluene is used for the preparation of the gold colloids.
3 re coimmobilized with biospecific species on gold colloids.
4 the conventional test strip based on colored gold-colloids.
5 eriments with horseradish peroxidase-labeled gold colloids and immunoelectron microscopy demonstrated
6 cells by systemically targeting tumours with gold colloids and locally applying near-infrared, low-en
7 -biotin in solution is added to biotinylated gold colloids and microwave heated, gold colloids did no
8 onspecific interactions between biotinylated gold colloids and streptavidin were negligible.
9 op assays based on fluorescence quenching by gold colloids, and to obtain directional radiation from
10 ences in measurement error using LoBs versus gold colloid are also described, as well as an assay for
11 differences of the SEIRA spectra obtained on gold colloid are compared to previous work on gold films
12                                              Gold colloids are well known to display strong plasmon a
13  by dynamic light scattering of ELP-modified gold colloids as a function of temperature.
14 ion of bovine serum albumin (BSA) to aqueous gold colloids can be quantified with molecular resolutio
15 otinylated bovine serum albumin-coated 20 nm gold colloids, cross-linked by additions of streptavidin
16 ased on the disassociation of dextran-coated gold colloids, cross-linked with Con A, by glucose.
17 inylated gold colloids and microwave heated, gold colloids did not aggregate, demonstrating that nons
18         Reports of the biogenic formation of gold colloids from gold complexes has also led to an inc
19  quantities of monodisperse thiol-stabilized gold colloids in toluene solution.
20                    The optical properties of gold colloid, including macroscopic ones such as color,
21                       The results for BSA on gold colloid nanoparticles can be modeled in terms of La
22 re reported as a function of accumulation of gold colloid on glass.
23                               Using the PCTP-gold colloid on magnetic microparticles the limit of det
24 ltiple extractions can be done with the PCTP-gold colloid on magnetic microparticles to further lower
25                                     The PCTP-gold colloid on magnetic microparticles was then used to
26                                  Immobilized gold colloid particles coated with a C-18 alkylsilane la
27  reacted with either streptavidin-conjugated gold colloid particles or fluorescently labeled neutravi
28 r 1-s microwave heating) of the biotinylated gold colloids reaches up to 10.5 m/s, which gives rise t
29                                          The gold colloid substrates are stable and exhibit reproduci
30 The detection antibodies are conjugated with gold colloids that are labeled with different Raman repo
31 of gold nanoparticles, (2) immobilization of gold colloids through the MIP's thiol groups, and (3) tr
32                  The abilities of LoBs and a gold colloid to detect cyanide are compared, and in both
33           Since Faraday's pioneering work on gold colloids, tremendous scientific research on plasmon
34                                 Biotinylated gold colloids were aggregated in solution with the addit
35 , a much more useful and simpler property of gold colloids, which has been ill explored with regard t

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