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1                                              FCCS analysis using EGFP and mCherry-tagged protein pair
2 orescence cross-correlation spectroscopy (3C-FCCS) has been shown to track assemblies of three spectr
3                Here, we clearly show that 3C-FCCS is capable of distinguishing beads barcoded with qu
4                                     Although FCCS could resolve this through cross-correlation, it su
5           The described lysate-based FCS and FCCS analysis may not only complement current biochemica
6  and cross-correlation spectroscopy (FCS and FCCS) are appealing technologies to study these macromol
7                              The CE/two-beam FCCS experiment described here is part of a family of te
8 nd unbound ssDNA were determined by two-beam FCCS within 2-6% precision, even for samples that contai
9 apurinic/apyrimidinic site, was monitored by FCCS using a double-stranded DNA substrate dual labeled
10           We use this information to correct FCCS measurements of the interaction of Cdc42, a small R
11                                           DC-FCCS offers the sensitivity and all other advantages of
12 tation of preformed dimers using SW-FCCS, DC-FCCS, quasi PIE-FCCS, and imaging FCCS.
13 al changes in the fluorescence intensity, DC-FCCS serves as a preferred means of measuring solution p
14                   We also show the use of DC-FCCS for monitoring competitive displacement of the labe
15 th a mAbs and demonstrated the utility of DC-FCCS in studies of antibody sandwiches, trimolecular for
16 orescence cross-correlation spectroscopy (DC-FCCS) was applied to study the binding interactions of m
17 plitude ratios of ~0.5 or less for different FCCS schemes.
18 ength FCCS and pulsed interleaved excitation FCCS to measure various tandem FPs constituted of differ
19 report the successful implementation of FCS, FCCS, and PCH in live yeast cells using fluorescent prot
20 ed fluorescence fluctuation techniques (FCS, FCCS, and PCH) required fractions between 7 and 11%.
21 id) of the enzyme using this cross-talk-free FCCS platform.
22 W-FCCS, DC-FCCS, quasi PIE-FCCS, and imaging FCCS.
23                   In addition, using imaging FCCS, we find that dimers have a tendency to be found at
24  Here, we combine several recent advances in FCCS apparatus and analysis to demonstrate it as an impo
25                                    Moreover, FCCS employing minute amounts of cells closely corrobora
26                              We also use MPE-FCCS to detect drug-protein interactions in the intracel
27 factors governing conformational behavior of FCCS containing systems.
28 on or cross-correlation spectroscopy (FCS or FCCS), a single molecule technique, has the ability to p
29                                          PIE-FCCS is a two-color fluorescence microscopy method that
30 esolved fluorescence spectroscopy called PIE-FCCS to resolve EGFR and EphA2 interactions in live cell
31 med dimers using SW-FCCS, DC-FCCS, quasi PIE-FCCS, and imaging FCCS.
32 rescence cross-correlation spectroscopy (PIE-FCCS) and fluorescence lifetime analysis.
33 rescence cross-correlation spectroscopy (PIE-FCCS).
34 rescence cross-correlation spectroscopy (PIE-FCCS).
35                                     With PIE-FCCS, we show that inactive PlexinA4 is dimerized in the
36 fluorescence cross-correlation spectroscopy (FCCS) and fluorescence recovery after photobleaching (FR
37 fluorescence cross-correlation spectroscopy (FCCS) and micro fabricated devices toward highly sensiti
38 fluorescence cross-correlation spectroscopy (FCCS) confirmed lateral mobility and the formation of sp
39 Fluorescence cross-correlation spectroscopy (FCCS) has been proposed and developed as a protein detec
40 Fluorescence cross-correlation spectroscopy (FCCS) is used to determine interactions and dissociation
41 fluorescence cross-correlation spectroscopy (FCCS) of live HEK cells transfected with 2 spectrally di
42 fluorescence cross-correlation spectroscopy (FCCS) to measure coreceptor/Lck codiffusion in situ.
43 fluorescence cross-correlation spectroscopy (FCCS) to structurally and quantitatively characterize NA
44 fluorescence cross-correlation spectroscopy (FCCS) was used to resolve the bound and unbound fraction
45 fluorescence cross-correlation spectroscopy (FCCS), and photon counting histograms (PCH) are fluctuat
46 fluorescence cross-correlation spectroscopy (FCCS), which provides a readout modality for the study o
47                         Here, we extend SPIM-FCCS by alternating laser excitation, which reduces fals
48 escence cross-correlation spectroscopy (SPIM-FCCS) and molecular dynamics modeling confirmed that c-F
49 he quantitation of preformed dimers using SW-FCCS, DC-FCCS, quasi PIE-FCCS, and imaging FCCS.
50 ng protocols and careful optimization of the FCCS instrumentation are essential to achieve the highes
51 on of alternating laser excitation (ALEX) to FCCS along with a method to exclude signals from occasio
52 nto the intracellular domain of CD4, we used FCCS to also show that stoichiometric coupling to Lck re
53 pecific association of dengue antibody using FCCS.
54                     We use single wavelength FCCS and pulsed interleaved excitation FCCS to measure v
55 t using microfluidic devices integrated with FCCS, both of which can be achieved practically, we shou