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1 served by analytical ultracentrifugation and fluorescence correlation spectroscopy.
2 on in black lipid membranes using dual-focus fluorescence correlation spectroscopy.
3 s well as 15-19 nm diameter probing areas in fluorescence correlation spectroscopy.
4 fluorescence microscopy in combination with fluorescence correlation spectroscopy.
5 hods, including single-particle tracking and fluorescence correlation spectroscopy.
6 h an automated spectroscopic system based on fluorescence correlation spectroscopy.
7 cterize complex protein assembly pathways by fluorescence correlation spectroscopy.
8 ding using circular dichroism and two-photon fluorescence correlation spectroscopy.
9 ent with DNA hybridization experiments using fluorescence correlation spectroscopy.
10 h background continues to be problematic for fluorescence correlation spectroscopy.
11 ase Abeta peptide with real-time imaging and fluorescence correlation spectroscopy.
12 ion peptide (pHLIP) in model membranes using fluorescence correlation spectroscopy.
13 per molecule than is achieved with confocal fluorescence correlation spectroscopy.
14 dback tracking microscopy and intramolecular fluorescence correlation spectroscopy.
15 ynamics within living cells using two-photon fluorescence correlation spectroscopy.
16 y or measured by alternative methods such as fluorescence correlation spectroscopy.
17 ependently demonstrated and quantified using fluorescence correlation spectroscopy.
18 fusion coefficient and fitting parameters in fluorescence correlation spectroscopy.
19 of fibroblasts and epithelial cells by using fluorescence correlation spectroscopy.
20 d QDs in aqueous solution is confirmed using fluorescence correlation spectroscopy.
21 adient sedimentation and in HeLa cells using fluorescence correlation spectroscopy.
22 rs, and their mobilities were analyzed using fluorescence correlation spectroscopy.
23 tate at pH 6.3, are reported, as measured by fluorescence correlation spectroscopy.
24 HSF diffusibility, as shown here directly by fluorescence correlation spectroscopy.
25 he nuclear pore of neuroblastoma cells using fluorescence correlation spectroscopy.
26 ion in the volume is important in two-photon fluorescence correlation spectroscopy.
27 ic fluid streaming which was also studied by fluorescence correlation spectroscopy.
28 efty inhibitors in live zebrafish embryos by fluorescence correlation spectroscopy.
29 orescence self-quenching in combination with fluorescence correlation spectroscopy.
30 s using an optical trap, and diffusion using fluorescence correlation spectroscopy.
31 nation of molecular dynamics simulations and fluorescence correlation spectroscopy.
32 Cherry-tagged beta1-integrins measured using fluorescence correlation spectroscopy.
33 llular concentrations can be estimated using fluorescence correlation spectroscopy.
34 evel using both single-particle tracking and fluorescence correlation spectroscopy.
35 techniques, including confocal detection and fluorescence-correlation spectroscopy.
36 tegrated dual-color dual-focus line-scanning fluorescence correlation spectroscopy (2c2f lsFCS) techn
37 ynamic light scattering (DLS), and two-focus fluorescence correlation spectroscopy (2f-FCS) to charac
39 efer methodology, was investigated by z-scan fluorescence correlation spectroscopy across a temperatu
42 n of a synthetic modular genetic system with fluorescence correlation spectroscopy allows us to direc
47 e effect of varying three key parameters for Fluorescence Correlation Spectroscopy analysis, first in
49 n live yeast, we developed a method coupling fluorescence correlation spectroscopy and calibrated ima
50 This dynamic evolution is monitored using fluorescence correlation spectroscopy and compared to a
54 fluorescence recovery after photobleaching, fluorescence correlation spectroscopy and electron micro
55 his stick-and-diffuse model accounts for the fluorescence correlation spectroscopy and fluorescence r
57 bly expressed in CHO cells and studied using fluorescence correlation spectroscopy and fluorescent br
61 echniques, namely cross-correlation scanning fluorescence correlation spectroscopy and number and bri
62 re widely used to analyze mobility data from fluorescence correlation spectroscopy and other experime
64 ntact cells by an established combination of fluorescence correlation spectroscopy and real-time trac
66 sion-based fluorescence techniques including fluorescence correlation spectroscopy and single particl
67 base subunit and alphaVbeta3 integrin using fluorescence correlation spectroscopy and single-particl
70 tracentrifugation, dynamic light scattering, fluorescence correlation spectroscopy, and electron micr
71 fluorescence recovery after photobleaching, fluorescence correlation spectroscopy, and extraction ex
72 s two single-molecule sensitivity technique, fluorescence correlation spectroscopy, and fluorescence-
73 pid developments in fluorescence microscopy, fluorescence correlation spectroscopy, and fluorescent l
75 orster resonance energy transfer, nanosecond fluorescence correlation spectroscopy, and microfluidic
76 tural studies using fluorescence anisotropy, fluorescence correlation spectroscopy, and size exclusio
77 ach that involves quantitative gel analysis, fluorescence correlation spectroscopy, and total interna
78 ity by Forster resonance energy transfer and fluorescence correlation spectroscopy; and segregation i
79 e fluorescence resonance energy transfer and fluorescence correlation spectroscopy are used to obtain
81 s in the plasma membrane of HEK293T cells by fluorescence correlation spectroscopy as well as fluores
82 ed tracer proteins were measured by means of fluorescence correlation spectroscopy at a total protein
83 correlation imaging, a multipoint version of fluorescence correlation spectroscopy, based upon a stat
86 an enhancement of the fluorescence signal in fluorescence correlation spectroscopy by a factor of two
87 influence of the field cage were studied by fluorescence correlation spectroscopy, circumventing pot
88 Using a combination of X-ray scattering, fluorescence correlation spectroscopy, coarse-grained mo
89 of Tau using size exclusion chromatography, fluorescence correlation spectroscopy, cross-linking fol
91 ing the maximum entropy method as adapted to fluorescence correlation spectroscopy data and compared
92 (FRET) and molecular brightness analysis of fluorescence correlation spectroscopy data from live HeL
94 introduce a simple approach for analysis of fluorescence correlation spectroscopy data that can full
97 to VWF, using microscale thermophoresis and fluorescence correlation spectroscopy (dissociation cons
99 ence resonance energy transfer (SP-FRET) and fluorescence correlation spectroscopy (FCS) also reveal
102 vesicles can be studied with solution-based fluorescence correlation spectroscopy (FCS) and can be i
106 scence recovery after photobleaching (FRAP), fluorescence correlation spectroscopy (FCS) and single-m
109 Device characterization is carried out using fluorescence correlation spectroscopy (FCS) and two-phot
110 nce recovery after photobleaching (FRAP) and fluorescence correlation spectroscopy (FCS) are the two
112 about binding to an immobile substrate from fluorescence correlation spectroscopy (FCS) autocorrelat
113 icle, we obtain analytic expressions for the fluorescence correlation spectroscopy (FCS) autocorrelat
120 performed (1)H pulsed-field gradient NMR and fluorescence correlation spectroscopy (FCS) experiments
121 f T4 ligase to dsDNA is also confirmed using fluorescence correlation spectroscopy (FCS) experiments,
125 ), in dissociating the Sp1-DNA complex using fluorescence correlation spectroscopy (FCS) in a microfl
126 ocyanine 540 (MC540), were first analyzed by fluorescence correlation spectroscopy (FCS) in different
127 cal temperature, pH and ionic strength using fluorescence correlation spectroscopy (FCS) in vitro.
136 nce recovery after photobleaching (FRAP) and fluorescence correlation spectroscopy (FCS) measurements
138 d using either fluctuation-based techniques (fluorescence correlation spectroscopy (FCS) or raster-sc
140 nuous fluorescence microphotolysis (CFM) and fluorescence correlation spectroscopy (FCS) permit measu
141 ividual lipids through a confocal volume via fluorescence correlation spectroscopy (FCS) provide a se
147 agonist, ABEA-X-BY630, and the technique of fluorescence correlation spectroscopy (FCS) to investiga
148 escence resonance energy transfer (FRET) and fluorescence correlation spectroscopy (FCS) to monitor t
152 le photon counting (TCSPC) was combined with fluorescence correlation spectroscopy (FCS) to study the
153 er a commercial instrument could be used for fluorescence correlation spectroscopy (FCS) under pulsed
156 serum albumin (BSA) into the nanoslits; and fluorescence correlation spectroscopy (FCS) was further
160 ing (high-speed) atomic force microscopy and fluorescence correlation spectroscopy (FCS) we found out
161 present study, this issue was examined using fluorescence correlation spectroscopy (FCS) with photon
162 plexus epithelial cells were evaluated using fluorescence correlation spectroscopy (FCS) with photon
163 to obtain by ensemble measurements, we used fluorescence correlation spectroscopy (FCS), a method th
164 aster image correlation spectroscopy (RICS), fluorescence correlation spectroscopy (FCS), and atomic
169 nce Recovery After Photobleaching (FRAP) and Fluorescence Correlation Spectroscopy (FCS), obtaining e
171 ce recovery after photobleaching (FRAP), and fluorescence correlation spectroscopy (FCS), to monitor
172 ent adenosine-A3 receptor (A3AR) agonist and fluorescence correlation spectroscopy (FCS), we demonstr
174 thioflavin T (ThT) fluorescence, NMR, EM and fluorescence correlation spectroscopy (FCS), we show tha
176 employed a unique analytical system based on fluorescence correlation spectroscopy (FCS), which measu
187 gh faster time resolution can be achieved by fluorescence-correlation spectroscopy (FCS), where inten
190 ion of Forster Resonance Energy Transfer and Fluorescence Correlation Spectroscopy (FRET-FCS) has a u
191 n of several spectroscopic techniques (e.g., fluorescence correlation spectroscopy, FRET, lifetime qu
195 uorescence anisotropy, light scattering, and fluorescence correlation spectroscopy, have not provided
197 als the number of SecYEG channels counted by fluorescence correlation spectroscopy in a single proteo
198 orescence recovery after photobleaching, and fluorescence correlation spectroscopy in Drosophila mela
199 ter resonance energy transfer and dual-color fluorescence correlation spectroscopy in studies with eG
202 contain inclusions of HTT, and analysis by a fluorescence correlation spectroscopy indicated that kno
206 , throughout the cell cycle demonstrate that fluorescence correlation spectroscopy is a powerful tool
208 n coefficient of Bdp-Chol, as measured using fluorescence correlation spectroscopy, is (7.4 +/- 0.3)
209 ained from rapid on-off kinetics revealed in fluorescence correlation spectroscopy, is 526 micros.
210 tudy using imaging total internal reflection-fluorescence correlation spectroscopy (ITIR-FCS) showed
211 e, independent techniques in parallel (e.g., fluorescence correlation spectroscopy, MALDI-MS, and flu
212 problem by using a combination of live-cell fluorescence correlation spectroscopy, mass spectrometry
213 from steady-state ensemble fluorescence and fluorescence correlation spectroscopy measurements both
215 nal diffusion coefficients are determined by fluorescence correlation spectroscopy measurements for p
222 ents using both ensemble and single-molecule fluorescence correlation spectroscopy measurements.
224 study, we addressed these questions by using fluorescence correlation spectroscopy, molecular dynamic
228 gyration and hydrodynamic radii estimated by fluorescence correlation spectroscopy of the two coexist
229 of individual HIV-1 particles using scanning fluorescence correlation spectroscopy on a super-resolut
230 and recovery with fructose was analyzed with fluorescence correlation spectroscopy on the level of a
231 ectron microscopy, dynamic light scattering, fluorescence correlation spectroscopy, optical spectrosc
232 ways can be distinguished in single-molecule fluorescence correlation spectroscopy or bulk time-resol
233 njected with fluorescent DNAs and studied by fluorescence correlation spectroscopy or photobleaching
236 n supported membranes using a combination of fluorescence correlation spectroscopy, photon counting h
237 e Fluorescence Resonance Energy Transfer and Fluorescence Correlation Spectroscopy provide quantitati
239 +/- 123 nM by microscale thermophoresis and fluorescence correlation spectroscopy, respectively).
241 transfection, was monitored using Two Photon Fluorescence Correlation Spectroscopy, revealing concent
242 per-resolution STED microscopy with scanning fluorescence correlation spectroscopy (scanning STED-FCS
246 n using single plane illumination microscopy-fluorescence correlation spectroscopy (SPIM-FCS), a mult
247 uperresolution STED microscopy combined with fluorescence correlation spectroscopy (STED-FCS) to acce
248 g optical STED nanoscopy in combination with fluorescence correlation spectroscopy (STED-FCS), a tech
250 imultaneously performing tens or hundreds of fluorescence correlation spectroscopy-style measurements
252 In addition, thanks to the multiconfocal fluorescence correlation spectroscopy system, up to five
253 Consistent with this, we found by using fluorescence correlation spectroscopy that a third of di
254 noprecipitation, in vitro cross-linking, and fluorescence correlation spectroscopy that hnRNP E1 bind
257 s at the level of individual molecules using fluorescence correlation spectroscopy, thereby avoiding
258 n, which is not observed at the experimental fluorescence correlation spectroscopy timescales (>100 m
261 er-resolution microscopy in combination with fluorescence correlation spectroscopy to assess the char
262 fluorescence lifetime imaging microscopy and fluorescence correlation spectroscopy to assess the form
264 the overall sizes of large RNAs, we employed fluorescence correlation spectroscopy to examine the hyd
266 asis for this PC-dependent behavior, we used fluorescence correlation spectroscopy to explore enzyme
269 e, we used imaging total internal reflection-fluorescence correlation spectroscopy to investigate EGF
270 ence resonance energy transfer (SM-FRET) and fluorescence correlation spectroscopy to investigate the
271 n order to explain these effects, we applied fluorescence correlation spectroscopy to investigate the
272 y of the Ran-RCC1 complex in living cells by fluorescence correlation spectroscopy to investigate whe
273 le for size-dependent DNA diffusion, we used fluorescence correlation spectroscopy to measure the dif
275 fluorescence lifetime imaging microscopy and fluorescence correlation spectroscopy to study functiona
276 uorescence recovery after photobleaching and fluorescence correlation spectroscopy, to examine the dy
277 t analysis spectroscopy, in combination with fluorescence correlation spectroscopy, to follow the pop
278 tilize a novel technique, ultrafast-scanning fluorescence correlation spectroscopy, to measure the mo
279 we use a single-molecule optical technique--fluorescence correlation spectroscopy--to probe the dena
280 We show that in comparison to traditional fluorescence correlation spectroscopy, tracking provides
281 ics of PLC-beta3 binding to Galphaq FRET and fluorescence correlation spectroscopy, two physically di
282 developed a method of performing near-field fluorescence correlation spectroscopy via an array of pl
285 stem region for the liposome, as measured by fluorescence correlation spectroscopy, was also increase
286 ion magic angle spinning NMR as well as with fluorescence correlation spectroscopy we demonstrate tha
297 roscopy, biochemical interaction studies and fluorescence correlation spectroscopy, we show that in l
300 alphaS bound to planar membranes measured by fluorescence correlation spectroscopy were correlated.
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