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1 h an automated quantification laser scanning cytometer.
2 staining was also shown using the COPAS flow cytometer.
3 /Rel using ImageStream, a flow-based imaging cytometer.
4 ermined and cell cycle analyzed using a flow cytometer.
5 was revealed on the DNA fragment sizing flow cytometer.
6  tumor cross-sections using a laser scanning cytometer.
7 e measurements of microparticles with a flow cytometer.
8 yed and electrically addressed, enabling our cytometer.
9 a single-round infectivity assay with a flow cytometer.
10 n and propidium iodide (PI) uptake on a flow cytometer.
11 ET in both conventional fluorimeter and flow cytometer.
12 aries screened by PECS using a benchtop flow cytometer.
13  are required for identification on the flow cytometer.
14 an on-line cone-plate viscometer with a flow cytometer.
15 paraformaldehyde before analysis with a flow cytometer.
16 proyl] (NBD)-labeled PS detected in the flow cytometer.
17 ated antibodies and analyzed by using a flow cytometer.
18 em from unstained epithelial cells by a flow cytometer.
19 articles are determined by an automated flow cytometer.
20 caspase-1 activation were determined by flow cytometer.
21 tral as fewer cells are run through the flow cytometer.
22 BA formats using a standard three-laser flow cytometer.
23 -cell images obtained from a 3D imaging flow cytometer.
24 ance comparable to that of a commercial flow cytometer.
25  by benchmarking against a conventional flow cytometer.
26 both a custom, portable fluorimeter and flow cytometer.
27 llent correlation with the results from flow cytometer.
28 rkfield images of cells from an imaging flow cytometer.
29 ve analysis and sorting in a commercial flow cytometer.
30  progenitor cells (EPCs) was assayed by flow cytometer.
31 thout the need of special devices but a flow cytometer.
32 were quantified using an iCys laser scanning cytometer.
33 g conditions measured using the Luminex flow cytometer.
34 uspension cells using a high-throughput flow cytometer.
35 s assayed using whole yeast cells and a flow cytometer.
36 d by a commercial hydrodynamic focusing flow cytometer.
37  automated detection using a chip-based flow cytometer.
38 proaching that of a commercial benchtop flow cytometer.
39 nd a regular fluorescence microscope or flow cytometer.
40 e to achieve a low-cost, truly portable flow cytometer.
41 developed that can be readily used with flow cytometers.
42 duct accumulation traits using standard flow cytometers.
43 pplicability of our BAT on a variety of flow cytometers.
44 he opportunities for low-cost, point-of-care cytometers.
45 alytes of interest for immunoassays and flow cytometers.
46  on a scale far surpassing conventional flow cytometers.
47  from these large-scale, high-frequency flow cytometers.
48 ch wanted feature missing in almost all flow cytometers.
49 ut in manners fully compatible with existing cytometers.
50 P) T(SCM) cells with commonly available flow cytometers.
51 c columns, and characterizing them with flow cytometers.
52 of sensitivity compared to conventional flow cytometers.
53 ,000 cells/s) using a custom 3D imaging flow cytometer (3D-IFC) and dispensing cells in a first-in-fi
54                                    This flow cytometer 7-h protocol for testing the antifungal suscep
55                                 Using a flow-cytometer adapted for nematode profiling, we generated '
56 e of Amnis ImageStream(X) Mk II imaging flow cytometer afforded accurate analysis of calibration bead
57                                         Flow cytometer analysis of cultured cells indicated that babo
58                                  LSR-II flow cytometer analyzed Peyer patches and lamina propria isol
59  1.6, 0.064, and 1.6 ng/mL for the microflow cytometer and 1.6, 0.064, and 8.0 ng/mL for the commerci
60 ), 10(5), and 10(4) cfu/mL for the microflow cytometer and 10(3), 10(6), and 10(5) cfu/mL for the com
61 cy comparable with that of a commercial flow cytometer and can analyze as many as 17 000 particles/s.
62  were used for this analysis: laser scanning cytometer and confocal microscopy.
63 volution of nanoparticle populations by flow cytometer and discriminate between unbound and fluoresce
64 ey allograft may function as an in vivo flow cytometer and sort cells involved in rejection into urin
65 64 index was easily performed using our flow cytometer and staff, producing minimal alteration in cli
66  structure or function with a laser scanning cytometer and then perform the comet assay on the same c
67 is rely on complex instrumentation like flow cytometers and fluorescence microscopes, which are both
68 er than previously reported biophysical flow cytometers and single-cell mechanics tools, while creati
69 rypts, the cells were sorted by using a flow cytometer, and colony assays in soft agar were performed
70 o-reactors and a commercially available flow cytometer, and it can efficiently isolate novel biocatal
71 ia in liquid cultures using a bench-top flow cytometer, and the low-cost fluorescent dyes Calcein-AM
72 say), cell cycle progression (Accuri C6 Flow Cytometer), apoptosis and necrosis (Annexin V-FITC assay
73                             Traditional flow cytometers are capable of rapid cellular assays on the b
74                                Magnetic flow cytometers are one such solution for rapid cancer cellul
75 owerful laboratory instruments, such as flow cytometers, are generally too cumbersome for spaceflight
76 fects of intersample contamination in a flow cytometer assay.
77 beads can be identified with a standard flow cytometer at 1000 beads/s.
78                                 Microfluidic cytometers based on coulter principle have recently show
79 rication, and operation of two types of flow cytometers based on microfluidic devices made of a singl
80  performance of our cell-phone-based imaging cytometer by measuring the density of white blood cells
81 e could be read out and sorted for on a flow cytometer by using a highly sensitive fluorescent protei
82 evelopment of high throughput, parallel flow cytometers by precision focusing of flow cytometry align
83                                     The flow cytometer can extract high-resolution bright-field image
84                                         Flow cytometers can now analyze up to 50 parameters per cell
85 then hydrodynamically focused in a microflow cytometer capable of 4-color analysis (two wavelengths f
86 nstrate here a high-resolution spectral flow cytometer capable of acquiring Raman spectra of individu
87 We present a time-resolved microfluidic flow cytometer capable of characterizing the FRET-based dynam
88 e processing was integrated with a microflow cytometer capable of simultaneously detecting multiple t
89      A new generation of high-frequency flow cytometers collects up to several hundred samples per da
90           We present a portable imaging flow cytometer comprising a smartphone, a small-footprint opt
91                                  The SeaFlow cytometer continuously profiles microbial phytoplankton
92  cell-phone-enabled optofluidic imaging flow cytometer could especially be useful for rapid and sensi
93 f simultaneous events on a dual-channel flow cytometer designed specifically for virus counting.
94 me-labeled affinity reagent, our paper-based cytometer detects WBCs according to their immunophenotyp
95 and evaluate the potential of a miniaturized cytometer developed for POC testing.
96                                Yet most flow cytometers do not accommodate live organisms of the size
97 veloped as a droplet-based microfluidic flow cytometer (Droplet-muFC) to comprehensively analyze mult
98 ogens could be detected and sorted in a flow cytometer, either alone or in association with epithelia
99 ange of DNA concentrations on a compact flow cytometer equipped with a frequency-doubled, diode-pumpe
100                  Further, the prototype flow cytometer equipped with an inertial focusing microchanne
101 that can be detected using conventional flow cytometers facilitating rapid analysis and purification
102              However, an ultrasensitive flow cytometer (FCM) developed in our lab has also demonstrat
103 lti-parametric measurement like optical flow cytometers (FCMs).
104                             The microfluidic cytometer focused the microspheres in three dimensions w
105 l properties and creates label-free chemical cytometer for cellular heterogeneity measurement.
106 mizing, calibrating and standardizing a flow cytometer for daily use.
107 be, or by processing samples on an automated cytometer for more granular information.
108 o the flow and moved them into the microflow cytometer for optical interrogation.
109  toward the creation of high throughput flow cytometers for rare cell detection applications (e.g., c
110 ein, we tested the Luminex 100, a novel flow cytometer, for the detection of the medically important
111 versing the interrogation volume of the flow cytometer from the first principles.
112      The multiplexed assays in the microflow cytometer had performance approaching that of a commerci
113                           The streaking mode cytometer has been used for the analysis of SYTO-9 label
114 se results indicate that the ultrasonic flow cytometer has the necessary performance for most flow cy
115                       Yet, conventional flow cytometers have fundamental limitations with regards to
116                            Microfluidic flow cytometers have largely followed the same path of techno
117                                Although flow cytometers have massive statistical power due to their s
118  cost of commercially available flow imaging cytometers, however, poses a steep financial barrier to
119                         In conventional-flow cytometers, hydrodynamics focus particles to the center
120 ter as the only hardware needed to give flow cytometers imaging capabilities.
121 is article, we review the impact of the flow cytometer in these areas of medical practice.
122  maintain the performance of individual flow cytometers in a facility.
123 ochrome-tagged probes and detected in a flow cytometer, indicating the mutation occurrence.
124 dardization) in this program when a new flow cytometer is installed or whenever the flow cytometer's
125           Creation of inexpensive small-flow cytometers is important for applications ranging from di
126 rn advances have yielded a new generation of cytometers, known as high-speed cell sorters.
127  this study, we introduce a light-field flow cytometer (LFC), an IFC system capable of high-content,
128 -uniform electric field in microfluidic flow cytometer like tapered electrodes, trapezoidal electrode
129                           The laser scanning cytometer (LSC) was able to provide the spatial distribu
130                                         Flow cytometers measure fluorescence and light scattering and
131 counts comparable to haemocytometer and flow cytometer measures (P = 0.54).
132 accuracy of our novel microfluidic impedance cytometer (MIC) was then tested by comparing same-site m
133 re then examined on each subset using a flow cytometer modified for high-sensitivity fluorescence mea
134 e the design of an impedimetric microfluidic cytometer on flexible substrate.
135 lines utilizing flow cytometry regardless of cytometer or panel design.
136 ice could be used in inexpensive stand-alone cytometers or as a part of integrated microanalysis syst
137  Cytophone, an innovative photoacoustic flow cytometer platform with high-pulse-rate lasers and a foc
138                      A parallel microfluidic cytometer (PMC) uses a high-speed scanning photomultipli
139 lipids) can be measured by a commercial flow cytometer, providing a convenient and sensitive detectio
140   However, sorting DE droplets with standard cytometers requires small droplets that can pass FACS no
141 erimental preparation process and use a flow cytometer's fluorescence channels that could otherwise b
142  cytometer is installed or whenever the flow cytometer's optical path is altered (e.g., lasers, filte
143 on, or whenever changes occur along the flow cytometer's optical path.
144 ermeability and light scatter using the flow cytometer showed a concentration dependence that was sim
145 lts confirm that the smartphone imaging flow cytometer (sIFC) is capable of both enumerating single p
146              In this study, we analyzed flow cytometer-sorted, AML blast-derived, and paired, buccal
147 thine reagent using a routine automated flow cytometer Sysmex XN20 (Sysmex, Kobe, Japan) and neutroph
148                    We describe a unique flow cytometer (TDI-SFC) for the immunophenotyping of low-abu
149 trode orientations in microfluidic MEMS flow cytometer technologies for effective manipulation of mic
150 roughput hydrogel-based platelet-contraction cytometer that quantifies single-platelet contraction fo
151               We present a microfluidic flow cytometer that rapidly assays 10(4)-10(5) member cell-ba
152 spheres and cells, the performance of a flow cytometer that uses acoustic energy to focus particles t
153 re we report a highly parallel acoustic flow cytometer that uses an acoustic standing wave to focus p
154 CytoFLEX is a novel semiconductor-based flow cytometer that utilizes avalanche photodiodes, wavelengt
155      In this work, the performance of a flow cytometer that was designed and custom-built specificall
156 n fluorescence intensity signals on the flow cytometer that were 2-4 times higher than assays perform
157 EM, EFM, FCM, as well as a custom-built flow cytometer (the Single Nanometric Particle Enumerator, SN
158                Although introduced in a flow cytometer, the new approach can also be straightforwardl
159 activated HUVEC, using a magnetical twisting cytometer, the observed resistance to the applied stress
160 h for on-the-fly analysis in an imaging flow cytometer.The interpretation of information-rich, high-t
161 ta1-integrin antibody and examined in a flow cytometer, there were 2 peaks of fluorescence.
162 e nanoballs through a microfluidic impedance cytometer, thus enabling a fully compact system with no
163   We applied QRBF in a high-throughput image cytometer to assess shape changes in Escherichia coli du
164                 We fabricated a microfluidic cytometer to characterize erythrocyte lysis kinetics.
165 t has been developed recently employs a flow cytometer to conduct high-throughput screening assays of
166  uses our specially designed 3D imaging flow cytometer to produce 3D cell images, our methodology can
167 le molecular components, which empowers mass cytometers to 'see' like pathologists.
168       Our work utilized the Luminex100 (flow cytometer) to detect TNT in a multiplexed displacement i
169          The multiplex assay requires a flow cytometer, two sets of latex particles coated with pneum
170 pensive and can be adapted for multiple flow cytometer types or software.
171 s in fluorescence-emission spectra, and flow cytometers typically perform cell measurements at one ti
172                                 Whereas most cytometers use fluorescent probes to ascertain the prese
173                                     The flow cytometers used in the study were calibrated with a stan
174 gram to optimize, calibrate and monitor flow cytometers used to measure cells labeled with five or mo
175 quality image of fast moving cells in a flow cytometer using PMT detectors, thus obtaining high throu
176 ing single-fluorophore sensitivity in a flow cytometer using quantum properties of single-photon emit
177                               The COPAS flow cytometer was highly accurate in the detection and measu
178 e sensitivity and accuracy of the COPAS flow cytometer was performed by analysis and sorting of unifo
179                       A microfabricated flow cytometer was used to demonstrate multiplexed detection
180 ering images obtained from a 3D imaging flow cytometer, we demonstrated key regulated cell types invo
181 esolution kinetic data extracted from a flow cytometer, we determined that there are two N-formyl pep
182 lly, the side scattering setting of the flow cytometer, which is associated with a 488 nm excitation
183              The method employs a novel flow cytometer with a dual laser system that allows the simul
184  tested the ability of a large-particle flow cytometer with a gentle pneumatic sorting mechanism to p
185 ta managements, we developed an imaging flow cytometer with a streak imaging mode capability.
186 e characterize the design and operation of a cytometer with a three-beam, probe/bleach/probe geometry
187 ed spores were further purified using a flow cytometer with cell sorting capabilities.
188  examine changes in LFA-1 affinity in a flow cytometer with live cells.
189                BSFC uses a custom-built flow cytometer with three excitation wavelengths (405 nm, 488
190 tial-temporal transformation to provide flow cytometers with cell imaging capabilities.

 
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