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1 alently immobilized onto a planar waveguide (microscope slide).
2 gle-walled carbon nanotubes deposited onto a microscope slide.
3 rated by using laminated inked patterns on a microscope slide.
4 ed oligonucleotides covalently attached to a microscope slide.
5 of interest are immobilized on a passivated microscope slide.
6 de down between 70 and 450 mum from a second microscope slide.
7 methylsiloxane on an indium-tin oxide coated microscope slide.
8 imately 4 microm of breast tissue on a glass microscope slide.
9 ained from a single drop of blood on a glass microscope slide.
10 osodium urate (MSU) crystals and placed on a microscope slide.
11 rase chain reactions (RT-PCRs) the size of a microscope slide.
12 reversibly bonded to a glass base such as a microscope slide.
13 eter-sized spots onto the surface of a glass microscope slide.
14 s within a thin acrylamide gel attached to a microscope slide.
15 ons on the surface of an avidin-coated glass microscope slide.
16 the final signal detection is performed on a microscope slide.
17 ls that were stuck by their heads to a glass microscope slide.
18 a thin polyacrylamide film poured on a glass microscope slide.
19 d to hold CDs and DVDs, was modified to hold microscope slides.
20 ed with formin FH1FH2 domains immobilized on microscope slides.
21 zed by a base-catalyzed sol-gel method, onto microscope slides.
22 unique cDNA sequences) printed on individual microscope slides.
23 n silicone elastomer sheets placed on top of microscope slides.
24 ast, eight or more at a time, using standard microscope slides.
25 s approach, beads are simply dropcast onto a microscope slide and dried into a monolayer film for dig
27 the electrode array is fabricated on a glass microscope slide and is operated in a simple electrochem
28 lement (waveguide) is created using a simple microscope slide and PDMS microfluidic architecture, all
29 e molecules within a polyacrylamide gel on a microscope slide and performing multiple amplifications
30 of the lesion; the tissue was smeared on one microscope slide and placed in a tube of 4 M guanidine t
32 A 10 mum thick tissue sample was placed on a microscope slide and was mounted tissue-side down betwee
33 te binding and recovery of DNA on flat glass microscope slides and compared their properties with com
35 valently immobilized on the surface of glass microscope slides and mechanically rubbed using a cloth.
36 roducing high hybridization signals on glass microscope slides, and CSO also protects the conductive
40 nm), resin-embedded serial sections on glass microscope slides, array tomography allows for quantitat
41 at surface and can be used in place of glass microscope slides as sample substrates that provide an i
42 pheres from a duplexed assay were mounted on microscope slides as well as inserted into wells etched
43 ensity is sufficiently large that a standard microscope slide can contain multiple replicates of ever
44 When induced to flow across mucus plated on microscope slides, cationic microbubbles demonstrated gr
45 an internal standard layer is deposited onto microscope slides containing either gelatin calibration
46 d on three different support substrates: (i) microscope slide coverslips; (ii) Al foil; and (iii) Cu
52 is abraded with the rough surface of a glass microscope slide having one frosted face; the sample is
55 We discovered that adhesion of flagella to a microscope slide is detrimental, reducing IFT train spee
56 lecule immobilization efficiency on standard microscope slides prepared using a well-characterized si
58 to integrating the two assay dimensions in a microscope slide-sized glass device, we introduce microf
61 xatives, sliced into thin sections placed on microscope slides, stained, and imaged to determine whet
63 s as cell capture agents on a functionalized microscope slide surface to assess their relative bindin
65 y is a simple and robust method of examining microscope slides, the preparation of the slides needed
67 scanning through the whole sample area of a microscope slide to locate every single target object of
68 hesion of bacteria to the borosilicate glass microscope slides used in an immunoarray biosensor forma
69 Silver island films (SIFs) grown on glass microscope slides were used as substrates for MEF DNA ar
70 rinted sol-gels, deposited as films on glass microscope slides, were shown to quantitatively detect D
71 sample or standards prepared across multiple microscope slides, which is indicative of the difficulti
73 nsity of 495,000 beads in the footprint of a microscope slide yielded 100% sensitivity for detecting