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1 sion electron microscopy, flow cytometry and dynamic light scattering.
2 asured by analytical ultracentrifugation and dynamic light scattering.
3 otein was assessed by circular dichroism and dynamic light scattering.
4 (CaCl2) electrolytes and using time-resolved dynamic light scattering.
5 toward diffusion coefficients determined by dynamic light scattering.
6 between a buffer and a model wine system by dynamic light scattering.
7 low-coherence interferometry and heterodyne dynamic light scattering.
8 ed techniques such as electron microscopy or dynamic light scattering.
9 with the core of NBD1, a model supported by dynamic light scattering.
10 s, cryogenic electron microscopy imaging and dynamic light scattering.
11 AFM, and 2), prevention of aggregation using dynamic light scattering.
12 ture-dependent sigmoidal kinetic curves, and dynamic light scattering.
13 X-ray scattering, X-ray crystallography, and dynamic light scattering.
14 l properties of NPs were characterized using dynamic light scattering.
15 er/diacetin/triacetin, were investigated via dynamic light scattering.
16 systematically studied through time-resolved dynamic light scattering.
17 a mean diameter of 150-200 nm as measured by dynamic light scattering.
18 itates, as measured here by turbidimetry and dynamic light scattering.
19 I) and caused expansion of FN as assessed by dynamic light scattering.
20 ich had a larger vesicle size as measured by dynamic light scattering.
21 tron paramagnetic resonance spectroscopy and dynamic light scattering.
22 7 and pH 2 by fluorescence spectroscopy and dynamic light scattering.
23 ed with transmission electron microscopy and dynamic light scattering.
24 ron and atomic force microscopies as well as dynamic light scattering.
25 , NMR, high resolution mass spectrometry and dynamic light scattering.
26 er time in acidic milieu, as investigated by dynamic light scattering.
27 raditional test-tube swelling experiment and Dynamic Light Scattering.
28 ed by intrinsic fluorescence measurement and dynamic light scattering, above the critical micellar co
29 l nanosystems were characterized by means of dynamic light scattering, AFM and cryoSEM, revealing sph
35 s were: phase behavior, droplet dimension by dynamic light scattering, analytical curve, and robustne
36 matography with multiangle light scattering, dynamic light scattering, analytical ultracentrifugation
37 al lattice by size exclusion chromatography, dynamic light scattering, analytical ultracentrifugation
39 sing macromolecular hydrodynamic techniques (dynamic light scattering and analytical ultracentrifugat
40 tion of nanosized aggregates was detected by dynamic light scattering and atomic force microscopy.
42 sing isothermal titration calorimetry (ITC), dynamic light scattering and cryogenic transmission elec
44 ure on casein micelle size, as determined by dynamic light scattering and differential centrifugation
45 -like particles (lentiVLPs) by western blot, dynamic light scattering and electron microscopy reveale
47 face charge (-30 to -41 mV), as confirmed by dynamic light scattering and electrophoretic mobility da
48 nalytical ultracentrifugation, reinforced by dynamic light scattering and environmental scanning elec
50 gation propensity of these compounds through dynamic light scattering and fractional solubility analy
51 ated by UV-visible spectroscopy, Viscometry, Dynamic light scattering and FT-IR spectroscopy techniqu
53 ere studied using fluorescence spectroscopy, dynamic light scattering and molecular dynamic simulatio
54 ture of the association pathway, assessed by dynamic light scattering and molecular dynamics simulati
55 lved, different NMR techniques combined with dynamic light scattering and molecular modeling contribu
60 de binding to CCR3 were analyzed by means of dynamic light scattering and nuclear magnetic resonance.
61 ing a novel approach involving time-resolved dynamic light scattering and parallel experiments design
62 ectroscopy, Circular Dichroism spectroscopy, Dynamic Light Scattering and Polyacrylamide Gel Electrop
63 dditionally, particle size distributions via dynamic light scattering and PTIR image analysis were fo
64 lver nanoparticles (AgNPs), a combination of dynamic light scattering and quartz crystal microgravime
65 UV-visible and Raman spectra, combined with dynamic light scattering and reactivity measurements.
66 via, UV-Vis spectroscopy, FTIR spectroscopy, dynamic light scattering and scanning electron microscop
69 DLs (NP-HDLs) were characterized in vitro by dynamic light scattering and size exclusion chromatograp
74 sensitized LPD (LPDS) were characterized by dynamic light scattering and transmission electron micro
75 ared at up to 17.5% w/w solids, as judged by dynamic light scattering and transmission electron micro
77 the silver nanoparticles were tracked using dynamic light scattering and transmission electron micro
78 ies of pure hybrids in water were studied by dynamic light scattering and transmission electron micro
79 es of aggregation properties of probes using dynamic light scattering and transmission electron micro
80 6 nm and a spherical shape, as determined by dynamic light scattering and transmission electron micro
82 re selected as optimum formulations based on dynamic light scattering and ultraviolet-visible spectro
84 oaded nanoparticles were characterized using dynamic light scattering and were found to have a diamet
85 ic and anionic model lipid assemblies, while dynamic light scattering and zeta potential measurements
86 on calorimetry (ITC), turbidity measurement, dynamic light scattering and zeta-potential analyses.
87 ation by monitoring hydrodynamic diameter by dynamic light scattering and zeta-potential under condit
89 sion chromatography, NMR relaxation studies, dynamic light scattering, and circular dichroism experim
90 sion electron and atomic force microscopies, dynamic light scattering, and computations reveal a diam
91 aphy, mass spectrometry, elemental analysis, dynamic light scattering, and electron microscopy techni
92 t projection NMR analyses with fluorescence, dynamic light scattering, and electron microscopy to elu
93 omplexes were characterized by turbidimetry, dynamic light scattering, and electron microscopy, respe
95 performed using both infrared spectroscopic, dynamic light scattering, and impedimetric spectroscopy
96 clusion chromatography and analyzed by STEM, dynamic light scattering, and multi-angle light scatteri
97 d by fluorescence resonance energy transfer, dynamic light scattering, and nanoparticle tracking anal
98 force microscopy, cryo-electron microscopy, dynamic light scattering, and polyacrylamide gel electro
99 ing SDS-PAGE, size-exclusion chromatography, dynamic light scattering, and real-time NMR analysis and
100 ere we used fluorescence titrations methods, dynamic light scattering, and single-molecule atomic for
101 tic properties of concentrated formulations, dynamic light scattering, and size-exclusion chromatogra
102 pproaches (transmission electron microscopy, dynamic light scattering, and spectrophotometry) for exp
103 s is measured by atomic force microscopy and dynamic light scattering, and the polyelectrolyte uptake
104 he size of casein micelles was determined by dynamic light scattering, and the water content and comp
105 s, including analytical ultracentrifugation, dynamic light scattering, and thermal stability assays,
107 petitive UV-vis and fluorescence titrations, dynamic light scattering, and transmission electron micr
108 asured using nanoparticle tracking analysis, dynamic light scattering, and ultraviolet-visible spectr
109 cterized using scanning electron microscopy, dynamic light scattering, and zeta potential analysis.
111 g their agglomeration-results obtained using dynamic light scattering at high particle concentrations
112 inetics were investigated with time-resolved dynamic light scattering at low monovalent salt concentr
113 ncluding polyacrylamide gel electrophoresis, dynamic light scattering, atomic force microscopy, and c
114 NMR spectroscopy, fluorescence spectroscopy, dynamic light scattering, atomic force microscopy, and t
116 s characterized using infrared spectroscopy, dynamic light scattering, atomic force microscopy, trans
118 and limitations, results obtained from batch dynamic light scattering (batch-DLS) and transmission el
119 Aggregation behavior was investigated using dynamic light scattering by monitoring the evolution of
121 techniques and complementary measurements of dynamic light scattering, CD, and soluble protein deplet
122 -ray diffraction, electron microscopy, FTIR, dynamic light scattering, cell viabilility assay, and an
124 naturing polyacrylamide gel electrophoresis, dynamic light scattering, confocal microscopy and atomis
125 alyzed by a combination of methods including dynamic light scattering, confocal microscopy, cryogenic
126 , NMR relaxation and diffusion measurements, dynamic light scattering, controlled proteolysis, gel el
129 uorescence recovery after photobleaching and dynamic light scattering data indicate that the liposome
131 stimator of particle size polydispersity for dynamic light scattering data, which quantifies the rela
134 e area of the shorter wavelength line and of dynamic light scattering-derived aggregate sizes show th
135 ICPMS to four established sizing techniques: dynamic light scattering, differential centrifugal sedim
136 ed on cryo-electron microscopy (cryo-EM) and dynamic light scattering (DLS) alpha-Syn lipoprotein par
137 EM), centrifugal liquid sedimentation (CLS), dynamic light scattering (DLS) and by measuring the Z-po
138 of the nanoemulsion droplets was measured by dynamic light scattering (DLS) and confirmed by transmis
139 o transmission electron microscopy (TEM) and dynamic light scattering (DLS) and confirmed the existen
140 f PEG vesicles (~1 nm size) was confirmed by dynamic light scattering (DLS) and confocal laser micros
142 onalized NPs to E2 in buffered water, we use dynamic light scattering (DLS) and resistive pulse sensi
144 MIP receptors were then characterised using dynamic light scattering (DLS) and transmission electron
145 -vis absorption, FT-IR, mercury-poison test, dynamic light scattering (DLS) and transmission electron
148 scopy (FTIR), Atomic Force Microscopy (AFM), Dynamic Light Scattering (DLS) and Ultraviolet-Visible (
149 nting, photopolymerized and characterized by dynamic light scattering (DLS) and UV/Vis spectroscopy.
151 , for a successful coating, was optimised by dynamic light scattering (DLS) and zeta potential measur
152 EM), transmission electron microscopy (TEM), dynamic light scattering (DLS) and zeta potential, respe
156 namics (DMD) simulations and high-throughput dynamic light scattering (DLS) experiments to study the
157 y X-ray photoelectron spectroscopy (XPS) and dynamic light scattering (DLS) experiments, which could
158 , centrifugal liquid sedimentation (CLS) and dynamic light scattering (DLS) have been used to give co
163 Transmission electron microscopy (TEM) and dynamic light scattering (DLS) measurements revealed bim
165 n was confirmed by (1)H NMR spectroscopy and dynamic light scattering (DLS) measurements, and its pho
168 scattering (MALS) detector with an embedded dynamic light scattering (DLS) module was introduced to
169 TEM) quantified particle size of 86.0 nm and dynamic light scattering (DLS) quantified hydrodynamic d
172 py (FTIR), Atomic Force Microscopy (AFM) and Dynamic Light Scattering (DLS) techniques are used to co
173 d by small-angle x-ray scattering (SAXS) and dynamic light scattering (DLS) techniques in the case of
174 ier-transform infrared spectroscopy (FT-IR), dynamic light scattering (DLS) techniques were used to s
177 onfirmed, after DEAE column purification, by dynamic light scattering (DLS) where the hydrodynamic ra
178 eal-time monitors, such as UV absorbance and dynamic light scattering (DLS), and an array of post-sep
179 opy, transmission electron microscopy (TEM), dynamic light scattering (DLS), and cyclic voltammetry (
180 sing transmission electron microscopy (TEM), dynamic light scattering (DLS), and electrophoretic mobi
181 d by X-ray photoelectron spectroscopy (XPS), dynamic light scattering (DLS), and infrared spectroscop
182 by using scanning electron microscopy (SEM), dynamic light scattering (DLS), and nanoparticle trackin
183 y using small-angle X-ray scattering (SAXS), dynamic light scattering (DLS), and NMR relaxation analy
184 charge detection mass spectrometry (CD-MS), dynamic light scattering (DLS), and transmission electro
185 reading the absorbance intensity transition, dynamic light scattering (DLS), and transmission electro
186 Fluorescence correlation spectroscopy (FCS), dynamic light scattering (DLS), and transmission electro
187 ster resonance energy transfer (FRET), SAXS, dynamic light scattering (DLS), and two-focus fluorescen
188 tography (SEC), microflow imaging (MFI), and dynamic light scattering (DLS), and water NMR (wNMR) tow
189 of techniques such as single-crystal X-ray, dynamic light scattering (DLS), electron paramagnetic re
190 anomaterials were characterized by XRD, FTIR dynamic light scattering (DLS), FESEM, HRTEM, and EDX sp
191 d by transmission electron microscopy (TEM), dynamic light scattering (DLS), Fourier-transform Infrar
192 the two via conventional techniques such as dynamic light scattering (DLS), nanoparticle tracking an
193 (FTIR), Scanning Electron Microscopy (SEM), Dynamic Light Scattering (DLS), Nuclear Magnetic Resonan
196 n SSW solutions was also characterized using dynamic light scattering (DLS), zeta potential, and quan
197 ic strength (IS) and type with time-resolved dynamic light scattering (DLS), zeta potential, and real
198 ogy of the TRH-PSA NPs were determined using dynamic light scattering (DLS), zeta-potential, and Scan
205 cterize their mechanical properties, whereas dynamic light scattering (DLS)and transmission electron
207 alized GNPs were analyzed by Zeta potential, dynamic light scattering, electron microscopy, and other
208 noprecipitation methods and characterised by dynamic light scattering, electron microscopy, encapsula
209 to shed light in the NEP sizing space (e.g. dynamic light scattering, electron microscopy, field flo
210 odification of CNTs by amine groups, whereas dynamic light scattering established the presence of pos
212 tion of isothermal titration calorimetry and dynamic light scattering experiments showed zinc binding
213 circular dichroism/infrared spectroscopy and dynamic light scattering experiments to highlight the du
217 ed monolayers (SAMs) and characterized using dynamic light scattering, extinction spectroscopy, zeta
218 onstrated by analytical ultracentrifugation, dynamic light scattering, fluorescence correlation spect
219 ination of transmission electron microscopy, dynamic light scattering, fluorescence correlation spect
220 f-assembled vesicles are characterized using dynamic light scattering, fluorescence microscopy, and N
223 in which correlated atomic force microscopy, dynamic light scattering, high performance liquid chroma
224 ration, transmission electron microscopy and dynamic light scattering identified nonfibrillar ~20-nm
226 yses by SEC, blue native PAGE, SDS-PAGE, and dynamic light scattering indicated that the resulting ma
227 ncy generation, atomic force microscopy, and dynamic light scattering, is attributed to increased cha
228 h an affinity in the low nanomolar range and dynamic light scattering measurements confirmed formatio
232 ng-coupled size exclusion chromatography and dynamic light scattering measurements showed that the po
234 in the presence of melittin is observed with dynamic light scattering measurements, and no increase i
235 H NMR spectroscopy, electron microscopy, and dynamic light scattering measurements, we postulated tha
240 ence reports beta-sheet fibril content while dynamic light scattering measures particle size distribu
241 onance spectroscopy, circular dichroism, and dynamic light scattering methods to demonstrate the reco
243 sequent purification and characterization by dynamic light scattering, NMR and toxicity neutralizatio
244 evidenced by size exclusion chromatography, dynamic light scattering, nuclear magnetic resonance ((1
245 n experimental techniques such as static and dynamic light scattering or sedimentation have prolifera
246 of GO were investigated using time-resolved dynamic light scattering over a wide range of aquatic ch
247 ments, transmission electron microscopy, and dynamic light scattering, provide compelling evidence th
248 c matter (NOM) were studied by time-resolved dynamic light scattering, quartz crystal microbalance, a
249 Finally, small-angle X-ray scattering and dynamic light scattering revealed similar binding modes
250 cal microscopy, atomic force microscopy, and dynamic light scattering revealed that such strands form
251 dissociation to activate the precatalyst and dynamic light scattering revealed the presence of nanopa
253 not reveal changes in LF structure; However, dynamic light scattering showed MR increased mean partic
255 lusion chromatography and particle sizing by dynamic light scattering showed that the protein was pur
259 etermined by analytical ultracentrifugation, dynamic light scattering, size exclusion chromatography,
260 a combination of Thioflavin T fluorescence, dynamic light scattering, size exclusion chromatography,
261 means of thioflavin T binding measurements, dynamic light scattering, size-exclusion chromatography,
262 r dichroism spectroscopy in combination with dynamic light scattering, size-exclusion chromatography,
263 say, antibody binding assay, gel filtration, dynamic light scattering, small angle x-ray scattering,
264 d by infrared and fluorescence spectroscopy, dynamic light scattering, small angle x-ray scattering,
265 conditions up to dynamical arrest, combining dynamic light scattering, small-angle x-ray scattering,
266 atography-multiangle laser light scattering, dynamic light scattering, small-angle x-ray scattering,
270 netics of folding and self-association using dynamic light scattering, stopped-flow fluorescence and
273 r combined titration, circular dichroism and dynamic light scattering study indicated that the change
275 A monomer followed by circular dichroism and dynamic light scattering suggest that it unfolds noncoop
276 in zeta potential and INP size, measured by dynamic light scattering, support that the contaminated
278 Transmission Electron Microscopic images and Dynamic Light Scattering technique shows that the algori
280 he aggregation process has been monitored by dynamic light scattering technique, while both enzyme en
284 (e.g., UV-vis absorption, FT-IR, (51)V NMR, dynamic light scattering, tetra-n-heptylammonium nitrate
285 tion and in situ by time-resolved static and dynamic light scattering, thereby precisely capturing th
287 use small-angle and total X-ray scattering, dynamic light scattering, transmission electron microsco
288 ted sol-gel transitions) was monitored using dynamic light scattering, transmission electron microsco
290 By using isothermal titration calorimetry, dynamic light scattering, UV/vis spectroscopy, and cryog
291 ing small-angle X-ray scattering, static and dynamic light scattering, viscometry, molecular dynamics
295 n microscopy, circular dichroism, static and dynamic light scattering, we have studied how RNA can in
296 an fluorescence, novel spectral fitting, and dynamic light scattering were combined to determine late
297 r flux across large pore membranes and using dynamic light scattering, with excellent agreement betwe
298 protein corona was characterized by means of dynamic light scattering, zeta potential, and liquid chr
299 n of pH and calcium addition using rheology, dynamic light scattering, zeta potential, surface tensio
300 ough different physicochemical measurements (dynamic light scattering, zeta-potential, and differenti