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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
6 nd unbound ssDNA were determined by two-beam FCCS within 2-6% precision, even for samples that contai
7 apurinic/apyrimidinic site, was monitored by FCCS using a double-stranded DNA substrate dual labeled
11 al changes in the fluorescence intensity, DC-FCCS serves as a preferred means of measuring solution p
13 th a mAbs and demonstrated the utility of DC-FCCS in studies of antibody sandwiches, trimolecular for
14 orescence cross-correlation spectroscopy (DC-FCCS) was applied to study the binding interactions of m
16 ength FCCS and pulsed interleaved excitation FCCS to measure various tandem FPs constituted of differ
17 report the successful implementation of FCS, FCCS, and PCH in live yeast cells using fluorescent prot
18 ed fluorescence fluctuation techniques (FCS, FCCS, and PCH) required fractions between 7 and 11%.
22 Here, we combine several recent advances in FCCS apparatus and analysis to demonstrate it as an impo
25 on or cross-correlation spectroscopy (FCS or FCCS), a single molecule technique, has the ability to p
32 fluorescence cross-correlation spectroscopy (FCCS) and fluorescence recovery after photobleaching (FR
33 fluorescence cross-correlation spectroscopy (FCCS) and micro fabricated devices toward highly sensiti
34 fluorescence cross-correlation spectroscopy (FCCS) confirmed lateral mobility and the formation of sp
35 Fluorescence cross-correlation spectroscopy (FCCS) has been proposed and developed as a protein detec
36 Fluorescence cross-correlation spectroscopy (FCCS) is used to determine interactions and dissociation
37 fluorescence cross-correlation spectroscopy (FCCS) was used to resolve the bound and unbound fraction
38 fluorescence cross-correlation spectroscopy (FCCS), and photon counting histograms (PCH) are fluctuat
39 fluorescence cross-correlation spectroscopy (FCCS), which provides a readout modality for the study o
40 escence cross-correlation spectroscopy (SPIM-FCCS) and molecular dynamics modeling confirmed that c-F
42 ng protocols and careful optimization of the FCCS instrumentation are essential to achieve the highes
43 on of alternating laser excitation (ALEX) to FCCS along with a method to exclude signals from occasio
46 t using microfluidic devices integrated with FCCS, both of which can be achieved practically, we shou
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