ライフサイエンスコーパス: cytometer

1 ance comparable to that of a commercial flow cytometer.

2 tumor cross-sections using a laser scanning cytometer.

3 e measurements of microparticles with a flow cytometer.

4 yed and electrically addressed, enabling our cytometer.

5 a single-round infectivity assay with a flow cytometer.

6 n and propidium iodide (PI) uptake on a flow cytometer.

7 ET in both conventional fluorimeter and flow cytometer.

8 aries screened by PECS using a benchtop flow cytometer.

9 are required for identification on the flow cytometer.

10 an on-line cone-plate viscometer with a flow cytometer.

11 paraformaldehyde before analysis with a flow cytometer.

12 proyl] (NBD)-labeled PS detected in the flow cytometer.

13 ated antibodies and analyzed by using a flow cytometer.

14 em from unstained epithelial cells by a flow cytometer.

15 ve analysis and sorting in a commercial flow cytometer.

16 llent correlation with the results from flow cytometer.

17 progenitor cells (EPCs) was assayed by flow cytometer.

18 thout the need of special devices but a flow cytometer.

19 were quantified using an iCys laser scanning cytometer.

20 g conditions measured using the Luminex flow cytometer.

21 uspension cells using a high-throughput flow cytometer.

22 s assayed using whole yeast cells and a flow cytometer.

23 d by a commercial hydrodynamic focusing flow cytometer.

24 automated detection using a chip-based flow cytometer.

25 rkfield images of cells from an imaging flow cytometer.

26 proaching that of a commercial benchtop flow cytometer.

27 nd a regular fluorescence microscope or flow cytometer.

28 e to achieve a low-cost, truly portable flow cytometer.

29 h an automated quantification laser scanning cytometer.

30 staining was also shown using the COPAS flow cytometer.

31 /Rel using ImageStream, a flow-based imaging cytometer.

32 ermined and cell cycle analyzed using a flow cytometer.

33 was revealed on the DNA fragment sizing flow cytometer.

34 developed that can be readily used with flow cytometers.

35 from these large-scale, high-frequency flow cytometers.

36 ch wanted feature missing in almost all flow cytometers.

37 ut in manners fully compatible with existing cytometers.

38 P) T(SCM) cells with commonly available flow cytometers.

39 c columns, and characterizing them with flow cytometers.

40 alytes of interest for immunoassays and flow cytometers.

41 on a scale far surpassing conventional flow cytometers.

42 This flow cytometer 7-h protocol for testing the antifungal suscep

43 Using a flow-cytometer adapted for nematode profiling, we generated '

44 e of Amnis ImageStream(X) Mk II imaging flow cytometer afforded accurate analysis of calibration bead

45 Flow cytometer analysis of cultured cells indicated that babo

46 LSR-II flow cytometer analyzed Peyer patches and lamina propria isol

47 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

48 ), 10(5), and 10(4) cfu/mL for the microflow cytometer and 10(3), 10(6), and 10(5) cfu/mL for the com

49 cy comparable with that of a commercial flow cytometer and can analyze as many as 17 000 particles/s.

50 were used for this analysis: laser scanning cytometer and confocal microscopy.

51 volution of nanoparticle populations by flow cytometer and discriminate between unbound and fluoresce

52 ey allograft may function as an in vivo flow cytometer and sort cells involved in rejection into urin

53 64 index was easily performed using our flow cytometer and staff, producing minimal alteration in cli

54 structure or function with a laser scanning cytometer and then perform the comet assay on the same c

55 er than previously reported biophysical flow cytometers and single-cell mechanics tools, while creati

56 rypts, the cells were sorted by using a flow cytometer, and colony assays in soft agar were performed

57 Traditional flow cytometers are capable of rapid cellular assays on the b

58 fects of intersample contamination in a flow cytometer assay.

59 beads can be identified with a standard flow cytometer at 1000 beads/s.

60 rication, and operation of two types of flow cytometers based on microfluidic devices made of a singl

61 performance of our cell-phone-based imaging cytometer by measuring the density of white blood cells

62 evelopment of high throughput, parallel flow cytometers by precision focusing of flow cytometry align

63 then hydrodynamically focused in a microflow cytometer capable of 4-color analysis (two wavelengths f

64 nstrate here a high-resolution spectral flow cytometer capable of acquiring Raman spectra of individu

65 We present a time-resolved microfluidic flow cytometer capable of characterizing the FRET-based dynam

66 e processing was integrated with a microflow cytometer capable of simultaneously detecting multiple t

67 A new generation of high-frequency flow cytometers collects up to several hundred samples per da

68 The SeaFlow cytometer continuously profiles microbial phytoplankton

69 cell-phone-enabled optofluidic imaging flow cytometer could especially be useful for rapid and sensi

70 f simultaneous events on a dual-channel flow cytometer designed specifically for virus counting.

71 and evaluate the potential of a miniaturized cytometer developed for POC testing.

72 ogens could be detected and sorted in a flow cytometer, either alone or in association with epithelia

73 ange of DNA concentrations on a compact flow cytometer equipped with a frequency-doubled, diode-pumpe

74 Further, the prototype flow cytometer equipped with an inertial focusing microchanne

75 that can be detected using conventional flow cytometers facilitating rapid analysis and purification

76 However, an ultrasensitive flow cytometer (FCM) developed in our lab has also demonstrat

77 The microfluidic cytometer focused the microspheres in three dimensions w

78 mizing, calibrating and standardizing a flow cytometer for daily use.

79 o the flow and moved them into the microflow cytometer for optical interrogation.

80 toward the creation of high throughput flow cytometers for rare cell detection applications (e.g., c

81 ein, we tested the Luminex 100, a novel flow cytometer, for the detection of the medically important

82 The multiplexed assays in the microflow cytometer had performance approaching that of a commerci

83 The streaking mode cytometer has been used for the analysis of SYTO-9 label

84 se results indicate that the ultrasonic flow cytometer has the necessary performance for most flow cy

85 Yet, conventional flow cytometers have fundamental limitations with regards to

86 Microfluidic flow cytometers have largely followed the same path of techno

87 Although flow cytometers have massive statistical power due to their s

88 In conventional-flow cytometers, hydrodynamics focus particles to the center

89 ter as the only hardware needed to give flow cytometers imaging capabilities.

90 is article, we review the impact of the flow cytometer in these areas of medical practice.

91 maintain the performance of individual flow cytometers in a facility.

92 ochrome-tagged probes and detected in a flow cytometer, indicating the mutation occurrence.

93 dardization) in this program when a new flow cytometer is installed or whenever the flow cytometer's

94 Creation of inexpensive small-flow cytometers is important for applications ranging from di

95 rn advances have yielded a new generation of cytometers, known as high-speed cell sorters.

96 The laser scanning cytometer (LSC) was able to provide the spatial distribu

97 Flow cytometers measure fluorescence and light scattering and

98 accuracy of our novel microfluidic impedance cytometer (MIC) was then tested by comparing same-site m

99 re then examined on each subset using a flow cytometer modified for high-sensitivity fluorescence mea

100 ice could be used in inexpensive stand-alone cytometers or as a part of integrated microanalysis syst

101 A parallel microfluidic cytometer (PMC) uses a high-speed scanning photomultipli

102 lipids) can be measured by a commercial flow cytometer, providing a convenient and sensitive detectio

103 cytometer is installed or whenever the flow cytometer's optical path is altered (e.g., lasers, filte

104 on, or whenever changes occur along the flow cytometer's optical path.

105 ermeability and light scatter using the flow cytometer showed a concentration dependence that was sim

106 In this study, we analyzed flow cytometer-sorted, AML blast-derived, and paired, buccal

107 thine reagent using a routine automated flow cytometer Sysmex XN20 (Sysmex, Kobe, Japan) and neutroph

108 roughput hydrogel-based platelet-contraction cytometer that quantifies single-platelet contraction fo

109 We present a microfluidic flow cytometer that rapidly assays 10(4)-10(5) member cell-ba

110 spheres and cells, the performance of a flow cytometer that uses acoustic energy to focus particles t

111 re we report a highly parallel acoustic flow cytometer that uses an acoustic standing wave to focus p

112 In this work, the performance of a flow cytometer that was designed and custom-built specificall

113 n fluorescence intensity signals on the flow cytometer that were 2-4 times higher than assays perform

114 EM, EFM, FCM, as well as a custom-built flow cytometer (the Single Nanometric Particle Enumerator, SN

115 Although introduced in a flow cytometer, the new approach can also be straightforwardl

116 activated HUVEC, using a magnetical twisting cytometer, the observed resistance to the applied stress

117 h for on-the-fly analysis in an imaging flow cytometer.The interpretation of information-rich, high-t

118 ta1-integrin antibody and examined in a flow cytometer, there were 2 peaks of fluorescence.

119 We applied QRBF in a high-throughput image cytometer to assess shape changes in Escherichia coli du

120 We fabricated a microfluidic cytometer to characterize erythrocyte lysis kinetics.

121 t has been developed recently employs a flow cytometer to conduct high-throughput screening assays of

122 Our work utilized the Luminex100 (flow cytometer) to detect TNT in a multiplexed displacement i

123 The multiplex assay requires a flow cytometer, two sets of latex particles coated with pneum

124 pensive and can be adapted for multiple flow cytometer types or software.

125 The flow cytometers used in the study were calibrated with a stan

126 gram to optimize, calibrate and monitor flow cytometers used to measure cells labeled with five or mo

127 quality image of fast moving cells in a flow cytometer using PMT detectors, thus obtaining high throu

128 The COPAS flow cytometer was highly accurate in the detection and measu

129 e sensitivity and accuracy of the COPAS flow cytometer was performed by analysis and sorting of unifo

130 A microfabricated flow cytometer was used to demonstrate multiplexed detection

131 esolution kinetic data extracted from a flow cytometer, we determined that there are two N-formyl pep

132 The method employs a novel flow cytometer with a dual laser system that allows the simul

133 ta managements, we developed an imaging flow cytometer with a streak imaging mode capability.

134 e characterize the design and operation of a cytometer with a three-beam, probe/bleach/probe geometry

135 ed spores were further purified using a flow cytometer with cell sorting capabilities.

136 examine changes in LFA-1 affinity in a flow cytometer with live cells.

137 tial-temporal transformation to provide flow cytometers with cell imaging capabilities.