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1 different pHs and ionic strengths (I) using quartz crystal microbalance.
2 imple model supported lipid bilayers using a quartz crystal microbalance.
3 NOM-coated silica surface was studied using quartz crystal microbalance.
4 ders of magnitude over a high-end commercial quartz crystal microbalance.
5 ked rigid monolayer on the gold surface of a quartz crystal microbalance.
6 olecules per impact event as determined by a quartz crystal microbalance.
7 ed with the gravimetric data obtained with a quartz crystal microbalance.
8 e thio-phosphorylated proteins quantified by quartz crystal microbalance.
9 columns containing glass collectors and on a quartz crystal microbalance.
10 orce-based biosensing technique based on the quartz crystal microbalance.
11 by MALDI-MS, surface plasmon resonance, and quartz crystal microbalances.
15 as characterized by electrochemical methods, quartz crystal microbalance and atomic force microscopy.
16 20 nm, was verified using an electrochemical quartz crystal microbalance and by atomic force microsco
19 e of LPS binding measurements via orthogonal quartz crystal microbalance and electrochemical readouts
20 upon air drying, as demonstrated by combined quartz crystal microbalance and ellipsometry measurement
21 The assembly of this system was followed by quartz crystal microbalance and grazing-incidence small-
22 (ethylene terephthalate), were studied using quartz crystal microbalance and sum frequency generation
23 d by time-resolved dynamic light scattering, quartz crystal microbalance, and atomic force microscopy
24 measured for the first time using a modified quartz crystal microbalance, and it is shown that ionic
25 e film and its swelling were measured with a quartz crystal microbalance, and the effects of fouling
26 fied gold surfaces has been studied with the quartz crystal microbalance, and the results suggest tha
27 ctDNA) were conducted with a flow-cell based quartz-crystal microbalance, and a binding constant of 2
28 motor protein (heavy meromyosin, HMM) using quartz crystal microbalance; and motor bioactivity with
29 ond that achievable with the lower-frequency quartz crystal microbalance approach, to measure smaller
30 developed for detection of insulin by using quartz crystal microbalances as transducers, in combinat
31 ation relies on laborious methods that use a quartz crystal microbalance, atomic force microscope, mi
33 l monolayers, validated by the techniques of quartz crystal microbalance, atomic force microscopy, an
34 hocholine (DPPC) phospholipid mixtures using quartz crystal microbalance-based nanoviscosity measurem
35 his report, we describe the development of a quartz crystal microbalance biosensor for detection of f
36 aces (on-rate/off-rate) was assessed using a quartz crystal microbalance biosensor revealing an incre
37 ls, both in solution and on the surface of a quartz crystal microbalance biosensor, reveal that the b
39 zymes to lignin surfaces, measured using the quartz crystal microbalance, correlates to the hydrophob
44 stance, as verified by simultaneous LSPR and quartz crystal microbalance-dissipation (QCM-D) measurem
46 ment approach that integrates a conventional quartz crystal microbalance-dissipation (QCM-D) setup wi
47 ee biosensing approach based on simultaneous quartz crystal microbalance-dissipation and ellipsometry
50 afted carboxyl groups (1-10%) was done using quartz crystal microbalance, electrochemical impedance s
52 including X-ray photoelectron spectroscopy, quartz crystal microbalance, ellipsometry, contact angle
54 de as well as on gold-coated electrochemical quartz crystal microbalance (EQCM) electrode by electrop
58 MHz quartz resonators of the electrochemical quartz crystal microbalance (EQCM) without affecting the
59 lication of five techniques: electrochemical quartz crystal microbalance (EQCM), square wave voltamme
61 yme film thickness, and the mass uptake from quartz crystal microbalance experiments, correlate with
63 ation, isothermal titration calorimetry, and quartz crystal microbalance) for interpreting the nature
66 chitecture is shown to outperform commercial quartz-crystal microbalances in terms of sensitivity.
71 addition, using a combination of dissipative quartz crystal microbalance measurements and neutron ref
74 c measurements of electroactive protein with quartz crystal microbalance measurements of total protei
83 and therefore demonstrate the ability of the quartz-crystal microbalance method not only to detect an
84 ew interference-free multichannel monolithic quartz crystal microbalance (MQCM) platform for bio-sens
86 sium zinc oxide (MZO) nanostructure-modified quartz crystal microbalance (MZOnano-QCM) biosensor to d
87 al assays using single molecule analyses and quartz crystal microbalance of the released IgG showed t
88 d by XPS and ellipsometry on dried films and quartz crystal microbalance on wet films, which appear l
92 rophilic (OH) surfaces, investigated using a quartz crystal microbalance (QCM) and grazing angle infr
93 onance (SPR) assays, Impedance-based method, Quartz Crystal Microbalance (QCM) and paper based detect
94 tyrene coated biosensor chip and housed in a quartz crystal microbalance (QCM) apparatus, the kinetic
95 work, we describe a combined microarray and quartz crystal microbalance (QCM) approach for the analy
96 The objective of this study was to develop a quartz crystal microbalance (QCM) aptasensor based on ss
98 nic liquids (ILs) as sensing materials and a quartz crystal microbalance (QCM) as a transducer was de
99 detection experiments were performed using a quartz crystal microbalance (QCM) as the sensing platfor
100 ibodies (scFv) as recognition elements and a quartz crystal microbalance (QCM) as the transducer.
101 ngle laser light scattering (MALLS), and the quartz crystal microbalance (QCM) as tools in investigat
102 ER2 receptor protein in piezoimmunosensor or quartz crystal microbalance (QCM) assays to detect Herce
103 orbent assays (ELISAs) and piezoimmunosensor/quartz crystal microbalance (QCM) assays were used to ch
105 ions on unfixed cancer cell surfaces using a quartz crystal microbalance (QCM) biosensor was develope
108 reptavidin) and a rod-shaped DNA (47bp) to a quartz crystal microbalance (QCM) device in a suspended
109 devices, such as simple frequency monitoring quartz crystal microbalance (QCM) devices, have good cli
110 t in situ on to the surface of a gold-coated quartz crystal microbalance (QCM) electrode as a thin pe
111 itable for some types of research, including quartz crystal microbalance (QCM) experiments involving
112 of protein-carbohydrate interactions using a quartz crystal microbalance (QCM) flow-through system wi
113 use of liquid and air measurements with the quartz crystal microbalance (QCM) for quantitative analy
114 ed surface plasmonic resonance (LSPR) into a quartz crystal microbalance (QCM) for studying biochemic
115 Chemical sensors based on a polymer coated quartz crystal microbalance (QCM) generally present poor
116 athion antibodies to the gold electrode of a Quartz Crystal Microbalance (QCM) giving rise to very hi
117 st-like Burkitt's lymphoma Raji cells on the quartz crystal microbalance (QCM) gold electrode surface
128 Through the use of an elevated-temperature quartz crystal microbalance (QCM) method we call microsc
130 nique wetting behavior, on the response of a quartz crystal microbalance (QCM) resonator operating in
132 perature and viscosity during PCR process on quartz crystal microbalance (QCM) sensor and to increase
134 A) using surface plasmon resonance (SPR) and quartz crystal microbalance (QCM) sensor platforms in hu
135 esent study, a sensitive molecular imprinted quartz crystal microbalance (QCM) sensor was prepared by
137 tivity improvement of conventional (5-20MHz) quartz crystal microbalance (QCM) sensors remains an uns
139 ity, by coupling polymer micropillars with a quartz crystal microbalance (QCM) substrate to form a tw
142 S), differential pulse voltammetry (DPV) and quartz crystal microbalance (QCM) techniques are used fo
145 covalently attached to a planar gold-coated quartz crystal microbalance (QCM) through reaction with
146 can be used to modify the surface of a gold quartz crystal microbalance (QCM) to create a unique pi-
150 oth differential pulse voltammetry (DPV) and quartz crystal microbalance (QCM) to verify the changes
152 tless detection, both by electrochemical and Quartz Crystal Microbalance (QCM) transducers and by usi
153 ve room-temperature ionic liquid (RTIL) with quartz crystal microbalance (QCM) transduction is presen
154 ched to the surface of a gold electrode of a quartz crystal microbalance (QCM) via a covalent thiol-g
155 which meets all these requirements, based on Quartz Crystal Microbalance (QCM) was developed, analyti
159 as developed using a piezoelectric biosensor-quartz crystal microbalance (QCM) with antibody-function
160 by use of biochemical membrane flotation and quartz crystal microbalance (QCM) with dissipation.
161 d evaluation of an acoustic wave sensor, the quartz crystal microbalance (QCM), as a rapid immunosens
162 ic silica (SiO2) was investigated in situ by quartz crystal microbalance (QCM), atomic force microsco
163 in the force spectroscopy mode combined with quartz crystal microbalance (QCM), both applied to quant
164 y (XPS), scanning electron microscope (SEM), quartz crystal microbalance (QCM), contact angle (CA) an
165 (Con A) and glycogen and Con A-mannan using quartz crystal microbalance (QCM), cost and time efficie
167 roscopy, various electrochemical techniques, quartz crystal microbalance (QCM), Fourier transform inf
169 de bonds, on a gold substrate was studied by quartz crystal microbalance (QCM), surface plasmon reson
170 le strategy to conduct such monitoring using quartz crystal microbalance (QCM), thereby relating the
177 y using a label-free acoustic technique, the quartz crystal microbalance (QCM-D), and oligonucleotide
181 thin layers at atmospheric pressure grown on Quartz Crystal Microbalance-QCM electrodes for which the
182 aphite particles (1-2 microm) as coatings on quartz crystal microbalances (QCMs) for detection and mo
186 n, obtained in situ using an electrochemical quartz crystal microbalance, reveals that this unusual o
187 eir transport behavior was characterized via quartz crystal microbalance, sand column, spectrofluorom
189 c intermittent titration and electrochemical quartz crystal microbalance studies indicate the kinetic
190 The sensing architecture was confirmed with quartz crystal microbalance studies, and stir effects co
191 esults from the deposition experiments using quartz crystal microbalance suggested that the attachmen
193 c cell-surface interactions as measured by a quartz crystal microbalance technique are altered when t
194 emi-integral voltammetry, an electrochemical quartz crystal microbalance technique, and coulometry/el
197 xceeds that of surface plasmon resonance and quartz crystal microbalance techniques, and is sensitive
199 sistance upon binding and a microgravimetric quartz crystal microbalance that reflected in situ mass
200 ips among frequency changes on a film-coated quartz crystal microbalance, thickness changes, and dc r
201 bodies are tethered on the gold surface of a quartz crystal microbalance through the photonics immobi
202 o each tetrapeptide and deposited onto 20MHz quartz crystal microbalances to construct the gas sensor
203 MALDI-TOF mass spectrometry, and the use of quartz crystal microbalances to measure weight changes o
204 gold nanoparticles and deposited onto 20 MHz quartz crystal microbalances to realize gas sensors.
205 nsducers, interdigitated microelectrodes and quartz crystal microbalance, to determine the correlatio
207 (AFM) and the NS1 detection was followed by quartz crystal microbalance with (QCM-D) and without ene
208 r that detects estrogenic substances using a quartz crystal microbalance with a genetically engineere
211 e characterize the formation of OM-SBs using quartz crystal microbalance with dissipation (QCM-D) and
212 onto a gold surface for characterization by quartz crystal microbalance with dissipation (QCM-D) and
214 plementary atomic force microscopy (AFM) and quartz crystal microbalance with dissipation (QCM-D) mea
215 kinetic surface plasmon resonance (SPR) and quartz crystal microbalance with dissipation (QCM-D) mea
216 tibodies recognition and reversibility using quartz crystal microbalance with dissipation (QCM-D) mea
217 ed at illustrating the potentialities of the quartz crystal microbalance with dissipation (QCM-D) tec
219 ica, iron oxide, and alumina were applied in quartz crystal microbalance with dissipation (QCM-D) to
220 ion of an RO cross-flow membrane lab unit, a quartz crystal microbalance with dissipation (QCM-D), an
221 O2, Fe3O4 and gold was characterized using a quartz crystal microbalance with dissipation (QCM-d).
222 d non-specific binding were measured using a quartz crystal microbalance with dissipation (QCM-D).
223 adhesion and deposition using a flow-through quartz crystal microbalance with dissipation (QCM-D).
224 deling of the EPS layers were conducted in a quartz crystal microbalance with dissipation (QCM-D).
225 th silica surfaces were investigated using a quartz crystal microbalance with dissipation monitoring
226 rom silica surfaces was investigated using a quartz crystal microbalance with dissipation monitoring
227 ttering (DLS), zeta potential, and real-time quartz crystal microbalance with dissipation monitoring
228 tal oxide surfaces were investigated using a quartz crystal microbalance with dissipation monitoring
230 ently bound and immobilized onto sensors for quartz crystal microbalance with dissipation monitoring
231 ironmental surfaces was investigated using a quartz crystal microbalance with dissipation monitoring
233 ith model oxide surfaces (Al2O3, SiO2) using quartz crystal microbalance with dissipation monitoring
234 iological membranes was investigated using a quartz crystal microbalance with dissipation monitoring
235 on silica surfaces was investigated using a quartz crystal microbalance with dissipation monitoring
237 using both atomic force microscope (AFM) and quartz crystal microbalance with dissipation monitoring
238 posome immobilization was determined using a quartz crystal microbalance with dissipation monitoring
239 and ionic strength (I) on adsorption using a quartz crystal microbalance with dissipation monitoring
240 HepG2 cells was investigated in situ using a quartz crystal microbalance with dissipation monitoring
241 studied using packed column experiments and quartz crystal microbalance with dissipation monitoring
244 s length and conformation was examined using quartz crystal microbalance with dissipation monitoring
247 inding affinities as determined by ELISA and quartz crystal microbalance with dissipation monitoring
248 s of the vesicle assembly through the use of quartz crystal microbalance with dissipation monitoring
250 in films during enzymatic hydrolysis using a Quartz Crystal Microbalance with Dissipation monitoring
252 vity of hybridization were investigated by a quartz crystal microbalance with dissipation monitoring
253 nsitive to biomolecular interactions, namely quartz crystal microbalance with dissipation monitoring
257 equency generation spectroscopies along with quartz crystal microbalance with dissipation monitoring
258 e present work focuses on the application of quartz crystal microbalance with dissipation monitoring
259 Herein, we demonstrate the capability of the quartz crystal microbalance with dissipation monitoring
261 kinetics of SAv binding are characterized by quartz crystal microbalance with dissipation monitoring,
262 roscopy, surface plasmon resonance (SPR) and quartz crystal microbalance with dissipation monitoring.
263 ion of solution pH and ionic strength, using quartz crystal microbalance with dissipation monitoring.
264 By plotting the frequency shifts versus the quartz crystal microbalance with dissipation overtone nu
266 novel emerging acoustic technology, namely ''Quartz Crystal Microbalance with Dissipation'' (QCM-D) h
269 T we report for the first time that a QCM-D (Quartz Crystal Microbalances with Dissipation) based tec
271 lase activities at the picomolar level using quartz-crystal microbalance with dissipation monitoring
272 on the basis of experiments conducted with a quartz-crystal microbalance with dissipation monitoring.
273 is of nanometer-thin polyester films using a quartz-crystal microbalance with dissipation monitoring.
274 The immunosensor design was evaluated by quartz-crystal microbalance with dissipation, atomic for
275 ls (BAEC) using a ZnO nanostructure-modified quartz crystal microbalance (ZnOnano-QCM) biosensor.
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