ライフサイエンスコーパス: flow cytometer

1 rformance comparable to that of a commercial flow cytometer.

2 sh them from unstained epithelial cells by a flow cytometer.

3 itative analysis and sorting in a commercial flow cytometer.

4 elial progenitor cells (EPCs) was assayed by flow cytometer.

5 ls without the need of special devices but a flow cytometer.

6 excellent correlation with the results from flow cytometer.

7 inding conditions measured using the Luminex flow cytometer.

8 e B suspension cells using a high-throughput flow cytometer.

9 2p was assayed using whole yeast cells and a flow cytometer.

10 ovided by a commercial hydrodynamic focusing flow cytometer.

11 e and automated detection using a chip-based flow cytometer.

12 ed darkfield images of cells from an imaging flow cytometer.

13 ce approaching that of a commercial benchtop flow cytometer.

14 nts and a regular fluorescence microscope or flow cytometer.

15 ssible to achieve a low-cost, truly portable flow cytometer.

16 zone staining was also shown using the COPAS flow cytometer.

17 s determined and cell cycle analyzed using a flow cytometer.

18 DNA) was revealed on the DNA fragment sizing flow cytometer.

19 scence measurements of microparticles with a flow cytometer.

20 s in a single-round infectivity assay with a flow cytometer.

21 lusion and propidium iodide (PI) uptake on a flow cytometer.

22 ge FRET in both conventional fluorimeter and flow cytometer.

23 libraries screened by PECS using a benchtop flow cytometer.

24 lours are required for identification on the flow cytometer.

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

26 e to paraformaldehyde before analysis with a flow cytometer.

27 inocaproyl] (NBD)-labeled PS detected in the flow cytometer.

28 onjugated antibodies and analyzed by using a flow cytometer.

29 a much wanted feature missing in almost all flow cytometers.

30 e (NHP) T(SCM) cells with commonly available flow cytometers.

31 gnetic columns, and characterizing them with flow cytometers.

32 to analytes of interest for immunoassays and flow cytometers.

33 ments on a scale far surpassing conventional flow cytometers.

34 been developed that can be readily used with flow cytometers.

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

36 This flow cytometer 7-h protocol for testing the antifungal s

37 Using a flow-cytometer adapted for nematode profiling, we genera

38 Use of Amnis ImageStream(X) Mk II imaging flow cytometer afforded accurate analysis of calibration

39 Flow cytometer analysis of cultured cells indicated that

40 LSR-II flow cytometer analyzed Peyer patches and lamina propria

41 ccuracy comparable with that of a commercial flow cytometer and can analyze as many as 17 000 particl

42 the evolution of nanoparticle populations by flow cytometer and discriminate between unbound and fluo

43 kidney allograft may function as an in vivo flow cytometer and sort cells involved in rejection into

44 he CD64 index was easily performed using our flow cytometer and staff, producing minimal alteration i

45 faster than previously reported biophysical flow cytometers and single-cell mechanics tools, while c

46 nic crypts, the cells were sorted by using a flow cytometer, and colony assays in soft agar were perf

47 Traditional flow cytometers are capable of rapid cellular assays on

48 he effects of intersample contamination in a flow cytometer assay.

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

50 , fabrication, and operation of two types of flow cytometers based on microfluidic devices made of a

51 the development of high throughput, parallel flow cytometers by precision focusing of flow cytometry

52 demonstrate here a high-resolution spectral flow cytometer capable of acquiring Raman spectra of ind

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

54 A new generation of high-frequency flow cytometers collects up to several hundred samples p

55 This cell-phone-enabled optofluidic imaging flow cytometer could especially be useful for rapid and

56 sis of simultaneous events on a dual-channel flow cytometer designed specifically for virus counting.

57 pathogens could be detected and sorted in a flow cytometer, either alone or in association with epit

58 ide range of DNA concentrations on a compact flow cytometer equipped with a frequency-doubled, diode-

59 Further, the prototype flow cytometer equipped with an inertial focusing microc

60 tein that can be detected using conventional flow cytometers facilitating rapid analysis and purifica

61 However, an ultrasensitive flow cytometer (FCM) developed in our lab has also demon

62 optimizing, calibrating and standardizing a flow cytometer for daily use.

63 mpact toward the creation of high throughput flow cytometers for rare cell detection applications (e.

64 Herein, we tested the Luminex 100, a novel flow cytometer, for the detection of the medically impor

65 These results indicate that the ultrasonic flow cytometer has the necessary performance for most fl

66 Yet, conventional flow cytometers have fundamental limitations with regard

67 Microfluidic flow cytometers have largely followed the same path of t

68 Although flow cytometers have massive statistical power due to th

69 In conventional-flow cytometers, hydrodynamics focus particles to the ce

70 l filter as the only hardware needed to give flow cytometers imaging capabilities.

71 In this article, we review the impact of the flow cytometer in these areas of medical practice.

72 e and maintain the performance of individual flow cytometers in a facility.

73 fluorochrome-tagged probes and detected in a flow cytometer, indicating the mutation occurrence.

74 standardization) in this program when a new flow cytometer is installed or whenever the flow cytomet

75 Creation of inexpensive small-flow cytometers is important for applications ranging fr

76 Flow cytometers measure fluorescence and light scatterin

77 PO were then examined on each subset using a flow cytometer modified for high-sensitivity fluorescenc

78 ospholipids) can be measured by a commercial flow cytometer, providing a convenient and sensitive det

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

80 llation, or whenever changes occur along the flow cytometer's optical path.

81 e impermeability and light scatter using the flow cytometer showed a concentration dependence that wa

82 In this study, we analyzed flow cytometer-sorted, AML blast-derived, and paired, bu

83 olymethine reagent using a routine automated flow cytometer Sysmex XN20 (Sysmex, Kobe, Japan) and neu

84 We present a microfluidic flow cytometer that rapidly assays 10(4)-10(5) member ce

85 microspheres and cells, the performance of a flow cytometer that uses acoustic energy to focus partic

86 Here we report a highly parallel acoustic flow cytometer that uses an acoustic standing wave to fo

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

88 median fluorescence intensity signals on the flow cytometer that were 2-4 times higher than assays pe

89 for TEM, EFM, FCM, as well as a custom-built flow cytometer (the Single Nanometric Particle Enumerato

90 Although introduced in a flow cytometer, the new approach can also be straightfor

91 enough for on-the-fly analysis in an imaging flow cytometer.The interpretation of information-rich, h

92 he beta1-integrin antibody and examined in a flow cytometer, there were 2 peaks of fluorescence.

93 n that has been developed recently employs a flow cytometer to conduct high-throughput screening assa

94 Our work utilized the Luminex100 (flow cytometer) to detect TNT in a multiplexed displacem

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

96 inexpensive and can be adapted for multiple flow cytometer types or software.

97 The flow cytometers used in the study were calibrated with a

98 e program to optimize, calibrate and monitor flow cytometers used to measure cells labeled with five

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

100 The COPAS flow cytometer was highly accurate in the detection and

101 of the sensitivity and accuracy of the COPAS flow cytometer was performed by analysis and sorting of

102 A microfabricated flow cytometer was used to demonstrate multiplexed detec

103 ime resolution kinetic data extracted from a flow cytometer, we determined that there are two N-formy

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

105 ed data managements, we developed an imaging flow cytometer with a streak imaging mode capability.

106 solated spores were further purified using a flow cytometer with cell sorting capabilities.

107 77 to examine changes in LFA-1 affinity in a flow cytometer with live cells.

108 f spatial-temporal transformation to provide flow cytometers with cell imaging capabilities.