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1 highly specific biological recognition (BSW biochip).
2 ty purification; (iii) biotin-mediated ChIP (bioChIP).
3 ept to produce the flow-through microfluidic biochip.
4 rate the usefulness and potential of the DNA biochip.
5 iguration was miniaturized and fitted onto a biochip.
6 was also improved using this newly designed biochip.
7 validate the results obtained by the new DNA-biochip.
8 tive antibodies to construct a GNR multiplex biochip.
9 positive (SK-BR-3) cells on the Test Cancer BioChip.
10 as AMS, MALDI-MS or protein microarray-type biochips.
11 s, and the development of protein arrays and biochips.
12 and precise voltage signal between different biochips.
13 photocorroding GaAs/AlGaAs quantum well (QW) biochips.
14 ly used methods for quantitative analysis on biochips.
15 es multiplexed biodetection and multi-marker biochips.
16 development of next generation point-of-care biochips.
17 iffused methods for quantitative analysis on biochips.
18 ts and for the design of cell-free synthetic biochips.
19 mmobilized on the surface of the GaAs/AlGaAs biochips.
20 poration into high-throughput biosensors and biochips.
21 high sensitivity obtained by the OLED based biochip (0.37ng/mul) and the short time required for the
22 we assembled dense DNA polymer brushes on a biochip along a density gradient and directly measured t
23 ly sensitive surface plasmon resonance (SPR) biochip and a simple portable imaging setup for label-fr
25 g potential for future applications, such as biochip and in situ imaging, which require reusability,
29 icrotechnology, cell culture in microfluidic biochips, and metabolic profiling opens the development
30 ng technologies including mass spectrometry, biochips, and single molecule analysis are included in t
31 g technologies (including mass spectrometry, biochips, and single-molecule analysis) will also be exa
33 r and cellular interactions occurring on the biochip are monitored by surface plasmon resonance (SPR)
34 n the design and fabrication of microfluidic biochips are protein binding on the channel surface and
36 This approach is anticipated to be a useful biochip array amenable to low-cost point-of-care devices
38 molecular machine, including fabrication of biochip arrays, and experimental studies of its ability
42 terized a miniaturized, highly-sensitive DNA biochip based on a deep-blue organic light-emitting diod
43 we designed and characterized a miniaturized biochip based on a novel deep-blue organic light-emittin
44 can be further transformed onto miniaturized biochips based on the nanosized optical transducer to al
47 rate was further increased on a Hsp60-coated biochip by 60% when a dielectrophoresis force was applie
49 c systems because the price and size of each biochip can be effectively reduced by using fully polyme
50 The biofunctionality of the ZIF-8-protected biochip can be restored by a simple water-rinsing step,
51 onally, some of the techniques, such as cDNA biochip, cannot define the sub-population of tissue from
52 rm known as the digital array, a nanofluidic biochip capable of accurately quantitating genes of inte
58 teria after 12-weeks storage of freeze-dried biochips, demonstrating the biochip potential as a simpl
59 iniature diode laser with the self-contained biochip design allows for a compact system that is readi
60 dinone phosphate) is combined with a compact biochip detection system, which includes a miniature dio
64 trate is an essential prelude to any hybrid "biochip" device, but a second and equally important cond
66 tiae and Chlamydia trachomatis with a single biochip, enabling a quick screening thanks to the presen
69 the developed material in the biosensors and biochips field, DNA probes were electrografted, using di
72 ene expression in localized DNA brushes on a biochip has been shown to depend on gene density and ori
77 lso evaluated in the context of carbohydrate biochips in which surface coating with carbohydrates is
78 e report a polymer/paper hybrid microfluidic biochip integrated with loop-mediated isothermal amplifi
79 developed arsenic-sensitive electrochemical biochip is easy to use and outperforms state-of-the-art
83 ased on indirect immunofluorescence, we used biochip mosaics of frozen brain sections (rat, monkey) a
84 triction model was applied to a miniaturized biochip nanovolume reactor to accurately characterize DN
87 with the paper-free non-hybrid microfluidic biochip over a period of three months, the hybrid microf
90 onucleotide probes on an in situ synthesized biochip platform, we demonstrate that mismatches in the
91 of freeze-dried biochips, demonstrating the biochip potential as a simple minimal maintenance "plug-
96 n removes baseline shifts within and between biochip sensors, allowing accurate and precise voltage s
97 d limitations in cost and reliability of the biochip, specificity of the antibody against Asian in-fi
103 ed portable bioaerosol sampler and miniature biochip system detected 100 B. globigii spores, correspo
105 the micron-sized particle trap integrated in biochip systems using a planar structure to generate an
110 lysis are implemented within sealed flexible biochips, time-consuming processing steps are not requir
112 TGA) was used on the surface of the proposed biochip to form a thiolate-modified sensing surface for
114 which harnesses surface acoustic wave (SAW) biochips, to detect HIV in a finger prick of blood withi
115 an interdigitated array microelectrode based biochip was developed and validated with pure AI H5 viru
117 iod of three months, the hybrid microfluidic biochip was found to have a much longer shelf life.
120 low are achievable with the magnetoresistive biochip, when pre-processing and chemometrics are used.
122 y, we developed a novel plastic microfluidic biochip with an on-chip anesthetic biosensor that was ch
127 onal instruments, the developed microfluidic biochips with on-chip MIP biosensors present the advanta
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