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1 nimal when 50% of the glass surface area was silanized.
2 cator with acrylamide on the distal end of a silanized 125 micrograms diameter multimode optical fibe
3 were treated first with a heterobifunctional silanizing agent and reacted subsequently with a vinyl m
4             Passivating the PCR chip using a silanizing agent followed by a polymer treatment resulte
5                        Then the ZnO-NRs were silanized and covalently modified by Protein-A (Glass/Zn
6                 Then, the sensor surface was silanized and directly aminated with (3-aminopropyl) tri
7                     The coated whiskers were silanized and manually blended with resins by spatulatio
8  The most successful strategy utilized amino-silanized controlled pore glass beads, which were couple
9 occal protein A (SPA) was used to modify the silanized fiber surface thus forming a SPA layer, which
10                           Nile red and a new silanized form of nile red that can be covalently attach
11  produced diameters of 1274 +/- 94 microm on silanized glass and 839 +/- 28 microm on PMMA.
12                  It was determined that both silanized glass and PMMA gave working optodes, but the o
13 eters of 895 +/- 26 and 688 +/- 54 microm on silanized glass and PMMA, respectively, and the 0.50-mm
14 - 80 and 1279 +/- 85 microm were obtained on silanized glass and PMMA, respectively, using the polypr
15  covalently bound to the inside surface of a silanized glass capillary column and the antigen-binding
16 re fabricated with methacrylate monomers and silanized glass fillers (CHX or CHX@MSN + glass filler p
17 d by Langmuir-Schafer deposition onto either silanized glass or existing Langmuir-Blodgett supported
18                 We immobilized magainin I on silanized glass slides using biotin-avidin chemistry, as
19 t DNA arrays compared to those fabricated on silanized glass slides.
20                                       Two un-silanized glass surfaces, RCA-cleaned and immersed in Tr
21 l substratum surfaces, i.e., clean glass and silanized glass surfaces, were studied.
22  on the biochemical activity of DNA fixed to silanized glass surfaces.
23 mine-terminated polyamidoamine dendrimer and silanized glass through an amide bond.
24 different insulating surfaces such as glass, silanized glass, or PTFE.
25                                              Silanized glass, poly(methyl methacrylate) (PMMA), polyc
26 e of aqueous solutions on the surface of the silanized glass.
27 igonucleotides in distilled water onto amino-silanized glass.
28 g in solution and deposited onto aminopropyl silanized glass.
29 ups, including plastic microtiter plates and silanized glass.
30 ts was performed in situ using self-adhesive silanized humic derivatives.
31                                Consequently, silanized humic materialas can be seen as both molecular
32 with tip orifice radii of 0.7-20 microm with silanized inner walls filled with a solution of 10 mM va
33 ng anti-TNT and anti-RDX antibodies onto the silanized inner walls using a hetero-bifunctional crossl
34  charged 3-aminopropyl triethoxysilane (APS) silanized mica.
35 ide polymer that is attached covalently to a silanized optical fiber tip surface by photocontrolled p
36                                  Half of the silanized particles received an additional heat treatmen
37 on, surface hydration, silanization solvent, silanizing reagent, catalysis, endcapping, and polymeriz
38 simple passivation of the PCR chamber with a silanizing reagent, reproducible DNA extraction and ampl
39  7-octenyltrimethoxysilane were evaluated as silanizing reagents in combination with poly(vinylprroli
40 ological evaluation of a number of different silanizing reagents, polymeric coatings, and polymer net
41 volved in (AD) biomarker detection onto this silanized surface by fluorescent microscopy.
42 The results demonstrated that the controlled silanized surface provides a novel and viable way to det
43 y formed a dense monolayer on a hydrophobic (silanized) surface.
44             Variation in the affinity of the silanized surfaces for DNA was compensated by precoating
45 the percentage of the glass surface that was silanized; the rate of charge transfer was minimal when
46  glass) and positively charging areas (glass silanized with a cationic siloxane terminated with a qua
47 l ester to interior pore surfaces previously silanized with EtO(Me)(2)Si(CH(2))(3)NH(2).
48  their surfaces, and the nanostructures were silanized with octadecyldimethylmethoxysilane in the gas

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