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1 s in a single-round infectivity assay with a flow cytometer.
2 lusion and propidium iodide (PI) uptake on a flow cytometer.
3 ge FRET in both conventional fluorimeter and flow cytometer.
4  libraries screened by PECS using a benchtop flow cytometer.
5 lours are required for identification on the flow cytometer.
6 ates an on-line cone-plate viscometer with a flow cytometer.
7 e to paraformaldehyde before analysis with a flow cytometer.
8 inocaproyl] (NBD)-labeled PS detected in the flow cytometer.
9 onjugated antibodies and analyzed by using a flow cytometer.
10 sh them from unstained epithelial cells by a flow cytometer.
11 the particles are determined by an automated flow cytometer.
12 t neutral as fewer cells are run through the flow cytometer.
13 lex SBA formats using a standard three-laser flow cytometer.
14 ingle-cell images obtained from a 3D imaging flow cytometer.
15  and caspase-1 activation were determined by flow cytometer.
16 ation by benchmarking against a conventional flow cytometer.
17 d by both a custom, portable fluorimeter and flow cytometer.
18 rformance comparable to that of a commercial flow cytometer.
19  excellent correlation with the results from flow cytometer.
20 ed darkfield images of cells from an imaging flow cytometer.
21 itative analysis and sorting in a commercial flow cytometer.
22 elial progenitor cells (EPCs) was assayed by flow cytometer.
23 ls without the need of special devices but a flow cytometer.
24 inding conditions measured using the Luminex flow cytometer.
25 e B suspension cells using a high-throughput flow cytometer.
26 2p was assayed using whole yeast cells and a flow cytometer.
27 ovided by a commercial hydrodynamic focusing flow cytometer.
28 e and automated detection using a chip-based flow cytometer.
29 ce approaching that of a commercial benchtop flow cytometer.
30 nts and a regular fluorescence microscope or flow cytometer.
31 ssible to achieve a low-cost, truly portable flow cytometer.
32 zone staining was also shown using the COPAS flow cytometer.
33 s determined and cell cycle analyzed using a flow cytometer.
34 DNA) was revealed on the DNA fragment sizing flow cytometer.
35 scence measurements of microparticles with a flow cytometer.
36 ioproduct accumulation traits using standard flow cytometers.
37 and applicability of our BAT on a variety of flow cytometers.
38 to analytes of interest for immunoassays and flow cytometers.
39 ments on a scale far surpassing conventional flow cytometers.
40 ation from these large-scale, high-frequency flow cytometers.
41  a much wanted feature missing in almost all flow cytometers.
42 e (NHP) T(SCM) cells with commonly available flow cytometers.
43 gnetic columns, and characterizing them with flow cytometers.
44 evel of sensitivity compared to conventional flow cytometers.
45 been developed that can be readily used with flow cytometers.
46  to 1,000 cells/s) using a custom 3D imaging flow cytometer (3D-IFC) and dispensing cells in a first-
47                                         This flow cytometer 7-h protocol for testing the antifungal s
48                                      Using a flow-cytometer adapted for nematode profiling, we genera
49    Use of Amnis ImageStream(X) Mk II imaging flow cytometer afforded accurate analysis of calibration
50                                              Flow cytometer analysis of cultured cells indicated that
51                                       LSR-II flow cytometer analyzed Peyer patches and lamina propria
52 ccuracy comparable with that of a commercial flow cytometer and can analyze as many as 17 000 particl
53 the evolution of nanoparticle populations by flow cytometer and discriminate between unbound and fluo
54  kidney allograft may function as an in vivo flow cytometer and sort cells involved in rejection into
55 he CD64 index was easily performed using our flow cytometer and staff, producing minimal alteration i
56 optosis rely on complex instrumentation like flow cytometers and fluorescence microscopes, which are
57  faster than previously reported biophysical flow cytometers and single-cell mechanics tools, while c
58 nic crypts, the cells were sorted by using a flow cytometer, and colony assays in soft agar were perf
59  micro-reactors and a commercially available flow cytometer, and it can efficiently isolate novel bio
60 acteria in liquid cultures using a bench-top flow cytometer, and the low-cost fluorescent dyes Calcei
61 UR Assay), cell cycle progression (Accuri C6 Flow Cytometer), apoptosis and necrosis (Annexin V-FITC
62                                  Traditional flow cytometers are capable of rapid cellular assays on
63                                     Magnetic flow cytometers are one such solution for rapid cancer c
64     Powerful laboratory instruments, such as flow cytometers, are generally too cumbersome for spacef
65 he effects of intersample contamination in a flow cytometer assay.
66  the beads can be identified with a standard flow cytometer at 1000 beads/s.
67 , fabrication, and operation of two types of flow cytometers based on microfluidic devices made of a
68 notype could be read out and sorted for on a flow cytometer by using a highly sensitive fluorescent p
69 the development of high throughput, parallel flow cytometers by precision focusing of flow cytometry
70                                          The flow cytometer can extract high-resolution bright-field
71                                              Flow cytometers can now analyze up to 50 parameters per
72  demonstrate here a high-resolution spectral flow cytometer capable of acquiring Raman spectra of ind
73      We present a time-resolved microfluidic flow cytometer capable of characterizing the FRET-based
74           A new generation of high-frequency flow cytometers collects up to several hundred samples p
75                We present a portable imaging flow cytometer comprising a smartphone, a small-footprin
76  This cell-phone-enabled optofluidic imaging flow cytometer could especially be useful for rapid and
77 sis of simultaneous events on a dual-channel flow cytometer designed specifically for virus counting.
78                                     Yet most flow cytometers do not accommodate live organisms of the
79 as developed as a droplet-based microfluidic flow cytometer (Droplet-muFC) to comprehensively analyze
80  pathogens could be detected and sorted in a flow cytometer, either alone or in association with epit
81 ide range of DNA concentrations on a compact flow cytometer equipped with a frequency-doubled, diode-
82                       Further, the prototype flow cytometer equipped with an inertial focusing microc
83 tein that can be detected using conventional flow cytometers facilitating rapid analysis and purifica
84                   However, an ultrasensitive flow cytometer (FCM) developed in our lab has also demon
85 ng multi-parametric measurement like optical flow cytometers (FCMs).
86  optimizing, calibrating and standardizing a flow cytometer for daily use.
87 mpact toward the creation of high throughput flow cytometers for rare cell detection applications (e.
88   Herein, we tested the Luminex 100, a novel flow cytometer, for the detection of the medically impor
89 s traversing the interrogation volume of the flow cytometer from the first principles.
90   These results indicate that the ultrasonic flow cytometer has the necessary performance for most fl
91                            Yet, conventional flow cytometers have fundamental limitations with regard
92                                 Microfluidic flow cytometers have largely followed the same path of t
93                                     Although flow cytometers have massive statistical power due to th
94                              In conventional-flow cytometers, hydrodynamics focus particles to the ce
95 l filter as the only hardware needed to give flow cytometers imaging capabilities.
96 In this article, we review the impact of the flow cytometer in these areas of medical practice.
97 e and maintain the performance of individual flow cytometers in a facility.
98 fluorochrome-tagged probes and detected in a flow cytometer, indicating the mutation occurrence.
99  standardization) in this program when a new flow cytometer is installed or whenever the flow cytomet
100                Creation of inexpensive small-flow cytometers is important for applications ranging fr
101    In this study, we introduce a light-field flow cytometer (LFC), an IFC system capable of high-cont
102 f non-uniform electric field in microfluidic flow cytometer like tapered electrodes, trapezoidal elec
103                                              Flow cytometers measure fluorescence and light scatterin
104 tion counts comparable to haemocytometer and flow cytometer measures (P = 0.54).
105 PO were then examined on each subset using a flow cytometer modified for high-sensitivity fluorescenc
106 e the Cytophone, an innovative photoacoustic flow cytometer platform with high-pulse-rate lasers and
107 ospholipids) can be measured by a commercial flow cytometer, providing a convenient and sensitive det
108 e experimental preparation process and use a flow cytometer's fluorescence channels that could otherw
109  flow cytometer is installed or whenever the flow cytometer's optical path is altered (e.g., lasers,
110 llation, or whenever changes occur along the flow cytometer's optical path.
111 e impermeability and light scatter using the flow cytometer showed a concentration dependence that wa
112  results confirm that the smartphone imaging flow cytometer (sIFC) is capable of both enumerating sin
113                   In this study, we analyzed flow cytometer-sorted, AML blast-derived, and paired, bu
114 olymethine reagent using a routine automated flow cytometer Sysmex XN20 (Sysmex, Kobe, Japan) and neu
115                         We describe a unique flow cytometer (TDI-SFC) for the immunophenotyping of lo
116  electrode orientations in microfluidic MEMS flow cytometer technologies for effective manipulation o
117                    We present a microfluidic flow cytometer that rapidly assays 10(4)-10(5) member ce
118 microspheres and cells, the performance of a flow cytometer that uses acoustic energy to focus partic
119    Here we report a highly parallel acoustic flow cytometer that uses an acoustic standing wave to fo
120  The CytoFLEX is a novel semiconductor-based flow cytometer that utilizes avalanche photodiodes, wave
121           In this work, the performance of a flow cytometer that was designed and custom-built specif
122 median fluorescence intensity signals on the flow cytometer that were 2-4 times higher than assays pe
123 for TEM, EFM, FCM, as well as a custom-built flow cytometer (the Single Nanometric Particle Enumerato
124                     Although introduced in a flow cytometer, the new approach can also be straightfor
125 enough for on-the-fly analysis in an imaging flow cytometer.The interpretation of information-rich, h
126 he beta1-integrin antibody and examined in a flow cytometer, there were 2 peaks of fluorescence.
127 n that has been developed recently employs a flow cytometer to conduct high-throughput screening assa
128  work uses our specially designed 3D imaging flow cytometer to produce 3D cell images, our methodolog
129            Our work utilized the Luminex100 (flow cytometer) to detect TNT in a multiplexed displacem
130               The multiplex assay requires a flow cytometer, two sets of latex particles coated with
131  inexpensive and can be adapted for multiple flow cytometer types or software.
132 erlaps in fluorescence-emission spectra, and flow cytometers typically perform cell measurements at o
133                                          The flow cytometers used in the study were calibrated with a
134 e program to optimize, calibrate and monitor flow cytometers used to measure cells labeled with five
135 high quality image of fast moving cells in a flow cytometer using PMT detectors, thus obtaining high
136 enabling single-fluorophore sensitivity in a flow cytometer using quantum properties of single-photon
137                                    The COPAS flow cytometer was highly accurate in the detection and
138 of the sensitivity and accuracy of the COPAS flow cytometer was performed by analysis and sorting of
139                            A microfabricated flow cytometer was used to demonstrate multiplexed detec
140 scattering images obtained from a 3D imaging flow cytometer, we demonstrated key regulated cell types
141 ime resolution kinetic data extracted from a flow cytometer, we determined that there are two N-formy
142 tionally, the side scattering setting of the flow cytometer, which is associated with a 488 nm excita
143                   The method employs a novel flow cytometer with a dual laser system that allows the
144 re we tested the ability of a large-particle flow cytometer with a gentle pneumatic sorting mechanism
145 ed data managements, we developed an imaging flow cytometer with a streak imaging mode capability.
146 solated spores were further purified using a flow cytometer with cell sorting capabilities.
147 77 to examine changes in LFA-1 affinity in a flow cytometer with live cells.
148                     BSFC uses a custom-built flow cytometer with three excitation wavelengths (405 nm
149 f spatial-temporal transformation to provide flow cytometers with cell imaging capabilities.

 
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