ライフサイエンスコーパス: fluorescence microscope

1 concentrations of Hg2+ using a conventional fluorescence microscope.

2 , and also in frozen cross-sections, under a fluorescence microscope.

3 F followed by EGF-Cy5.5 and examined under a fluorescence microscope.

4 cessed as frozen sections, and viewed with a fluorescence microscope.

5 n a custom-made observation platform under a fluorescence microscope.

6 ole dihydrochloride (DAPI) and imaged with a fluorescence microscope.

7 canning confocal microscope, and an inverted fluorescence microscope.

8 the CTIS combined with a commercial inverted fluorescence microscope.

9 ioning capability of a two-photon excitation fluorescence microscope.

10 e lens epithelial cells was monitored with a fluorescence microscope.

11 data obtained with standard filter sets in a fluorescence microscope.

12 ators and a laser scanning confocal or video fluorescence microscope.

13 dization and immunoanalysis monitored with a fluorescence microscope.

14 ecial stage and observed under an intravital fluorescence microscope.

15 d by the negative-staining appearance in the fluorescence microscope.

16 tion cross-flow membrane system mounted on a fluorescence microscope.

17 ellular markers and a miniature head-mounted fluorescence microscope.

18 Immunoagglutination can be observed under a fluorescence microscope.

19 y images Au(3+) in living HeLa cells under a fluorescence microscope.

20 tection is achieved using a smartphone-based fluorescence microscope.

21 obes, appearing as alternative bands under a fluorescence microscope.

22 ndividual codes identifiable using a typical fluorescence microscope.

23 isting fluorescence techniques on a standard fluorescence microscope.

24 axial and coronal images using a wide-field fluorescence microscope.

25 LAMP2 and LC3 with Rab7 was observed under a fluorescence microscope.

26 ionuclide uptake by single live cells with a fluorescence microscope.

27 zed and imaged individually using a confocal fluorescence microscope.

28 , and live cell motility GFP-tracking with a fluorescence microscope.

29 dual optical trap interlaced with a confocal fluorescence microscope.

30 s flat mounted, and images were taken with a fluorescence microscope.

31 tup for use with a widely available compound fluorescence microscope.

32 , and the microarray was imaged using an epi-fluorescence microscope.

33 f the microscope objective on a standard epi-fluorescence microscope.

34 performed in a single sample with a modified fluorescence microscope.

35 g/ml applied CTB could be observed under the fluorescence microscope.

36 led endocytic structures are examined with a fluorescence microscope.

37 astuzumab-(IRDye800)(m) and examined under a fluorescence microscope.

38 force trap (optical tweezers) on an inverted fluorescence microscope.

39 Images were recorded by fluorescence microscope.

40 recorded with confocal and light sheet-based fluorescence microscopes.

41 s not optimized for filters commonly used in fluorescence microscopes.

42 oach can also be straightforwardly used with fluorescence microscopes.

43 In a total internal reflection fluorescence microscope, an evanescence excitation field

44 Fluorescence microscope analysis detected microneme and

45 Confocal fluorescence microscope analysis indicates that in COS c

46 essive movement in total internal reflection fluorescence microscope analysis, demonstrating that myo

47 on in sarcomere lengths, and only requires a fluorescence microscope and a CCD camera.

48 bserved in living samples using a wide-field fluorescence microscope and a cooled charge-coupled devi

49 and transparent extracellular matrix using a fluorescence microscope and a simple forward data analys

50 ase-locked ultrasound lens into a two-photon fluorescence microscope and achieved microsecond-scale a

51 pe, we have developed a two-channel confocal fluorescence microscope and applied it to study the dyna

52 chnique is easy to implement with a standard fluorescence microscope and CCD camera.

53 rings, we built a customized single molecule fluorescence microscope and developed single particle tr

54 verall, providing both visualization under a fluorescence microscope and quantification after lysis i

55 forward and can be performed using a regular fluorescence microscope and standard molecular biology a

56 DNA is then quantitatively imaged with a fluorescence microscope and the fragments are sized to a

57 ning capability of the two-photon excitation fluorescence microscope and the partition and spectral p

58 ving organism by developing an image under a fluorescence microscope and useful to estimate the amoun

59 aboratory-on-a-chip applications, as typical fluorescence microscopes and charge-coupled device (CCD)

60 and single-molecule detection with standard fluorescence microscopes and inexpensive digital color c

61 at 37 degrees C on the stage of an inverted fluorescence microscope, and [Ca2+]i was measured using

62 nique is simple to implement on a commercial fluorescence microscope, and especially suitable for bio

63 ted directly from the culture dishes under a fluorescence microscope, and total DNA was then prepared

64 ns of living Caenorhabditis elegans, using a fluorescence microscope-based transport assay.

65 lateral and axial resolution of a wide-field fluorescence microscope but has been too slow for live i

66 y can double the resolution of the widefield fluorescence microscope but has previously been too slow

67 f lipid bilayers can be visualized under the fluorescence microscope, but the process is very fast an

68 ar radiotracers are imaged on a conventional fluorescence microscope by capturing individual flashes

69 ed sheets can be made highly visible under a fluorescence microscope by quenching the emission from a

70 detection sensitivity of a smartphone-based fluorescence microscope by using surface-enhanced fluore

71 herefore constructed a novel single-molecule fluorescence microscope capable of efficiently detecting

72 nd imaged using a total internal reflectance fluorescence microscope, cells exhibited sporadic fluore

73 ehavior in vivo and complements the existing fluorescence microscope characterization of CLIP-170 int

74 By using fluorescence microscope-charge-coupled device camera as

75 ce; detection was performed utilizing an epi-fluorescence microscope/charge coupled device imaging sy

76 th a research microscopist and by TBDx using fluorescence microscopes, classifying slides based on th

77 Existing super-resolution fluorescence microscopes compromise acquisition speed to

78 the NPs with polarized light on a wide-field fluorescence microscope enabled monitoring of both prote

79 center frequency of over 150 MHz and an epi-fluorescence microscope, entitled acoustic-transfection

80 Particle diffusometry requires only a fluorescence microscope equipped with a charge-coupled d

81 n of intracellular elastase activity using a fluorescence microscope equipped with standard optics.

82 be used as an add-on module to any standard fluorescence microscope even with low NA objectives.

83 Typically implemented on a fluorescence microscope, FCS samples femtoliter volumes

84 Here we describe a compact light sheet fluorescence microscope, featuring a 45 degrees inverted

85 By using a fluorescence microscope fitted with UV fluoride lenses,

86 dorsal tectum with a cooled CCD camera on a fluorescence microscope for 5 to 8 hours.

87 on, we developed a dedicated single molecule fluorescence microscope for detecting single ADAMTS13 mo

88 e the adaptation of a conventional widefield fluorescence microscope for FPALM and present step-by-st

89 We test this custom designed confocal fluorescence microscope for future use with brain clarif

90 strated on a commercially available inverted fluorescence microscope frame using the method of obliqu

91 g distance, and large field of view confocal fluorescence microscope (H(2)L(2)-CFM) with the capabili

92 d mouse embryos acquired with three types of fluorescence microscopes, (ii) scalability by analyzing

93 apply this technique to a series of confocal fluorescence microscope image sequences of mitochondria,

94 LIF system that identifies panels containing fluorescence microscope images among figures in online j

95 Fluorescence microscope images and FT-IR spectra were us

96 Results obtained from optical fluorescence microscope images and live/dead cytotoxicit

97 ches construct ordered restriction maps from fluorescence microscope images of individual, endonuclea

98 To verify DEP response, fluorescence microscope images were captured before and

99 Fluorescence microscope images were used to count PI-sta

100 n microscopy technique are: 1), the use of a fluorescence microscope in contrast with the confocal mi

101 right-green fluorescence was observed with a fluorescence microscope in virtually all examined tissue

102 We demonstrate an adaptive confocal fluorescence microscope incorporating this modal sensor

103 e fluorescence images captured by a handhold fluorescence microscope increases with increasing glucos

104 ary to the well known diffraction limit, the fluorescence microscope is in principle capable of unlim

105 cept, a 0.5 numerical aperture (NA) confocal fluorescence microscope is prototyped with a 3 mm x 3 mm

106 ts red-emitting state easily with a laser or fluorescence microscope lamp under conditions of low oxy

107 A novel fluorescence microscope/laser optical system was develop

108 of focus of a digitally scanned light-sheet fluorescence microscope (LSFM), multiple image planes ca

109 we introduce a miniature (1.9 g) integrated fluorescence microscope made from mass-producible parts,

110 bjects, then imaging them on cheap miniature fluorescence microscopes ("mini-microscopes"), it is pos

111 CoSMoS micromirror total internal reflection fluorescence microscope (mmTIRFM).

112 Digital images from fluorescence microscope movies of living cells are fed i

113 Portable, miniaturized fluorescence microscopes now allow brain imaging in free

114 response in Escherichia coli using standard fluorescence microscope optics for excitation at 440 +/-

115 ried out with either a trans-illuminated epi-fluorescence microscope or a fluorescence light box, bot

116 logy and cell culture reagents and a regular fluorescence microscope or flow cytometer.

117 rometric measurements on these cells using a fluorescence microscope or in cell suspension using a fl

118 ium response of the cells is measured with a fluorescence microscope photometry system.

119 m-sensitive fluorescent probe (fura-2) and a fluorescence microscope photometry system.

120 Electrophysiological and fluorescence microscope recordings performed in wild-typ

121 Images of the library under a fluorescence microscope revealed at least 40-50 differen

122 ted scanning-angle total internal reflection fluorescence microscope (SA-TIRFM).

123 fiber-based time-resolved near-infrared (IR) fluorescence microscope successfully coupled lifetime di

124 calibrated single-beam optical trap within a fluorescence microscope system, one can measure forces a

125 Here, we present a light sheet fluorescence microscope that achieves 390 nm isotropic r

126 resent a simple modification to a wide-field fluorescence microscope that addresses both challenges a

127 (GFP), and then assayed processivity using a fluorescence microscope that can visualize single kinesi

128 d the accuracy of CellScope, a novel digital fluorescence microscope that may expand access to micros

129 These investigations became possible with a fluorescence microscope that was modified for recording

130 Compatible with readily accessible fluorescence microscopes, these easy-to-use membrane DNA

131 Through the use of a conventional fluorescence microscope, this method demonstrates a forc

132 g-angle prism-type total internal reflection fluorescence microscope (TIRFM) was constructed and test

133 Total internal reflection fluorescence microscope (TIRFM) was used for optical ima

134 Slides were examined with a fluorescence microscope to detect the presence of male c

135 by SPORT, we constructed a dual-modality DIC/fluorescence microscope to simultaneously image fluoresc

136 Our method uses custom epi-fluorescence microscopes to automatically image single c

137 toreceptors were obtained using conventional fluorescence microscopes to image through the lens of th

138 en face in a wholemount preparation under a fluorescence microscope, to evaluate the distribution of

139 visualized at the single-molecule level in a fluorescence microscope upon isothermal amplification an

140 Many commercial as well as custom-built fluorescence microscopes use scientific-grade cameras th

141 mplemented on a conventional reflected-light fluorescence microscope using materials and resources th

142 The multistacking was verified under a fluorescence microscope using Rhodamine 6G as the analyt

143 of intact, living tadpoles with conventional fluorescence microscopes, using the lens of the tadpole

144 e limit of detection determined with a basic fluorescence microscope was 0.006 mug l(-1) (30 pM); thi

145 A smartphone-based fluorescence microscope was fabricated as a handheld in

146 A confocal fluorescence microscope was used to observe the fluoresc

147 ing a digital camera attached to an inverted fluorescence microscope, we acquired images at 1 frame/s

148 n of the newly developed lattice light-sheet fluorescence microscope, we reexamined their assembly dy

149 sing the sectioning effect of the two-photon fluorescence microscope, we studied the behavior of phos

150 Using a miniature fluorescence microscope, we tracked the Ca(2+) dynamics

151 lation methods for FRET quantification using fluorescence microscopes were compared.

152 ian cells was also observed under a confocal fluorescence microscope when the treated cells were expo

153 molecule counting using an epi-illumination, fluorescence microscope with charge-coupled device detec

154 an inexpensive video camera and an ordinary fluorescence microscope with mercury-arc or strobed lase

155 properties were obtained by using a confocal fluorescence microscope with picosecond time resolution.

156 ion of and emission by fluorophores, the way fluorescence microscopes work, and some of the ways fluo