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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
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
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
17 inylated gold colloids and microwave heated, gold colloids did not aggregate, demonstrating that nons
24 ltiple extractions can be done with the PCTP-gold colloid on magnetic microparticles to further lower
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
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
35 , a much more useful and simpler property of gold colloids, which has been ill explored with regard t
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