ライフサイエンスコーパス: fluorescent indicator

1 ial chromosome (BAC) transgenes containing a fluorescent indicator.

2 dene)methyl)benzothiazol ium (TO-PRO) as the fluorescent indicator.

3 he 1-hydroxypyrene-3,6,8-trisulfonate (HPTS) fluorescent indicator.

4 le reaction between phosphoryl halides and a fluorescent indicator.

5 N-ethylquinolinium chloride, a Cl--sensitive fluorescent indicator.

6 s considerably greater than that reported by fluorescent indicators.

7 +]i), and Ca2+ ([Ca2+]i) using ion-sensitive fluorescent indicators.

8 of conventional biosensing methods, such as fluorescent indicators.

9 nderstanding their functions using synthetic fluorescent indicators.

10 plication of ion/pH-sensing, dual-wavelength fluorescent indicators.

11 uld be tuned by using either colorimetric or fluorescent indicators.

12 s by use of different commercially available fluorescent indicators.

13 reporter genes (lacZ, EGFP, ECFP, DsRed) or fluorescent indicators.

14 rations and distributions, and without using fluorescent indicators.

15 posomes colabeled with gadolinium (Gd) and a fluorescent indicator, 1,1'-dioctadecyl-3,3,3',3'-tetram

16 on the dye 6-carboxyfluoroscein (6C-Fl) as a fluorescent indicator; 2,2'-azobis-2-amidinopropane hydr

17 it heart was employed with the use of the NO fluorescent indicator 4,5-diaminofluorescein diacetate (

18 n NO synthase activity (assayed by using the fluorescent indicator 4,5-diaminofluorescein) and transl

19 -alpha-LA was also confirmed by means of the fluorescent indicator acrylodated fatty acid binding pro

20 signals in single CA1 neurons, injected with fluorescent indicators, after extended exposures to a lo

21 we describe a set of recombinase-responsive fluorescent indicator alleles in mice that significantly

22 Each sensor combines an ion-selective fluorescent indicator and an ion-insensitive internal st

23 tetramethylbenzobis(imidazolium) (MBBI) as a fluorescent indicator and resulted in the unexpected dis

24 Using fluorescent indicators and FRET-based probes, we found t

25 determined the pH of the cortical granule by fluorescent indicators and micro-pH probe measurements a

26 scribing the criteria for rational design of fluorescent indicators and the mathematical expressions

27 nitric oxide production was measured using a fluorescent indicator, and TLR7 expression was character

28 Current genetically encoded calmodulin-based fluorescent indicators are likely to distort fast Ca(2+)

29 rd currents (STOCs), are seen as sparks when fluorescent indicators are used.

30 opy using sodium, chloride, and pH-sensitive fluorescent indicators, ASL [Na+] was 97 +/- 5 mM, [Cl-]

31 luation of Formaldehyde Probe 1 (FP1), a new fluorescent indicator based on the 2-aza-Cope sigmatropi

32 ng segments were selectively loaded with the fluorescent indicator BCECF-AM.

33 lemmal store sites (seen as hot spots, using fluorescent indicators); Ca2+ waves then spread from the

34 Confocal Ca2+ imaging using the fluorescent indicator Calcium Green-1 revealed about twi

35 We have dubbed these fluorescent indicators 'cameleons'.

36 Using impermeant fluorescent indicators, capacitance measurements and ele

37 by continuous monitoring of pH(i), using the fluorescent indicator carboxy-seminaphthorhodafluor-1 (S

38 We have designed a novel fluorescent indicator composed of two green fluorescent

39 A tailor-made fluorescent indicator cross-linker was thus designed tha

40 oduction was assessed using the NO-sensitive fluorescent indicator DAF-2.

41 s, we visualized the TATS (labelled with the fluorescent indicator, Di-8-ANEPPS) simultaneously with

42 etry in conjunction with a voltage-sensitive fluorescent indicator dye (oxonol), we have identified a

43 The pH-sensitive fluorescent indicator dye 2', 7'-bis-(2-carboxyethyl)-5-

44 2+)](i)) as revealed by simultaneous DIC and fluorescent indicator dye microscopy.

45 ther caged species that can be chelated by a fluorescent indicator dye, as well as caged fluorescent

46 longus motor terminals using Ca2+-sensitive fluorescent indicator dyes (rhod-2, rhod-5F).

47 action of neurons at once, whereas synthetic fluorescent indicator dyes label tissue indiscriminately

48 opy in rodent cerebellar cortex labeled with fluorescent indicator dyes or the calcium-sensor protein

49 This study used fluorescent indicator dyes to measure changes in cytosol

50 Using two-photon excitation of fluorescent indicator dyes, we measured calcium concentr

51 fluxes of metal ions using a metal-sensitive fluorescent indicator encapsulated in proteoliposomes.

52 fabricated in a microemulsion and consist of fluorescent indicators entrapped in a polyacrylamide mat

53 ial [Mg(2+)] reported by an Mg(2+)-sensitive fluorescent indicator, exploiting the differential affin

54 natal mouse inner hair cells filled with the fluorescent indicator FLUO-3, revealed a transient incre

55 Using the calcium-specific fluorescent indicator fluo-3, we also found that C(2)-ce

56 imaging retinotectal axons labeled with the fluorescent indicator Fluo-4.

57 d with single photon confocal microscopy and fluorescent indicators fluo-4, CM-H(2)DCFDA and MitoSOX

58 islets with high temporal resolution using a fluorescent indicator, FluoZin-3.

59 with a phospholipid membrane that contains a fluorescent indicator for a targeted analyte.

60 A fluorescent indicator for Ca2+ called a yellow 'cameleon

61 Methyl-Ester (PY1-ME), a new chemoselective fluorescent indicator for H(2)O(2), directly demonstrate

62 e tested this hypothesis by using an in vivo fluorescent indicator for PtdIns(4,5)P2, by tagging the

63 onfirmed using two methods: (1) the use of a fluorescent indicator for the presence of double-strande

64 a bright red fluorescent voltage indicator (fluorescent indicator for voltage imaging red; FlicR1) w

65 Cameleons are genetically-encoded fluorescent indicators for Ca2+ based on green fluoresce

66 vercome this problem we have constructed new fluorescent indicators for Ca2+ that are genetically enc

67 The applicability of AVBs as fluorescent indicators for imaging cellular zinc(II), ho

68 ts of secreted fluid were microinjected with fluorescent indicators for measurement of [Na(+)], [Cl(-

69 tiometric, pH-resistant, genetically encoded fluorescent indicators for NADPH (iNap sensors) with var

70 As a family of novel fluorescent indicators for nitric oxide (NO), the diamin

71 in the design, synthesis and application of fluorescent indicators for pH, metal ions, anions, biomo

72 The leaching of fluorescent indicator from the polymer is less than 50%

73 ces in global Ca2+ levels monitored with the fluorescent indicator Fura Red that could account for ap

74 mouse cardiomyocytes loaded with the Ca(2+) fluorescent indicator Fura-2 acetoxymethyl ester.

75 red using a microspectrofluorometer with the fluorescent indicator fura-2, and tumor necrosis factor

76 measured in human platelets loaded with the fluorescent indicator fura-2.

77 in intracellular Ca(2+), as assessed by the fluorescent indicator fura-FF, being larger when NMDAR a

78 endothelial cells (CPAE cell line) with the fluorescent indicators fura-2 and DAF-2, respectively, r

79 [Ca2+]i and [Na+]i were monitored using the fluorescent indicators fura-2 and sodium-binding benzofu

80 d cGMP levels; cells were then loaded with a fluorescent indicator (Fura-2AM or sodium-binding benzof

81 We used the fluorescent indicators, fura-2 and magfura-2, which have

82 ctance and measurements of [Ca2+]i using the fluorescent indicator furaptra.

83 thesized calcium-selective, long-wavelength, fluorescent indicator has been constructed, with a respo

84 f optical microscopy and genetically encoded fluorescent indicators has become a widespread means of

85 ntensity in a region where the analyte and a fluorescent indicator have interdiffused.

86 [Ca2+]i was measured using the fluorescent indicator indo 1 in voltage-clamped ferret a

87 2+]i) was measured at 35 degrees C using the fluorescent indicator indo-1 in patch-clamped, single ut

88 ar myocytes loaded with the Ca(2+)-sensitive fluorescent indicator indo-1.

89 Cytoplasmic Ca2+ was monitored using the fluorescent indicator indo-1.

90 Cytoplasmic [Ca2+] was monitored using the fluorescent indicator indo-1.

91 ere performed in isolated myocytes using the fluorescent indicators Indo-1 (to measure [Ca2+]i) and S

92 ndothelial growth factor (VEGF)165 using the fluorescent indicators indo-1 AM and DiSBAC2(3), respect

93 ar [Ca2+] and [Sr2+] were monitored with the fluorescent indicator, indo-1.

94 canning microscopy of calcium dynamics using fluorescent indicators is a widely used imaging method f

95 with a second polymeric layer containing the fluorescent indicators is shown to yield identical sensi

96 s of disease and 'smart' genetically encoded fluorescent indicators, its use is now increasing expone

97 a by measuring changes in matrix [Ca2+] with fluorescent indicators loaded into motor terminal mitoch

98 3R), have generally used 45Ca2+-flux assays, fluorescent indicators loaded within either the cytosol

99 Using the fluorescent indicator mag-fura-2, the metal released fro

100 We have therefore used the Mg(2+)-sensitive fluorescent indicator Magnesium Green (MgG) to provide a

101 Acini were incubated with the fluorescent indicator molecule fura 2, and [Ca(2+)](i) w

102 A naphthalimide-based fluorescent indicator monomer 1 for the integration into

103 The fluorescent indicator of FFA, ADIFAB (acrylodan-labeled

104 trate similarly to GTP, making BGTP a useful fluorescent indicator of G protein activity.

105 for the uptake of YO-PRO-1, a small-molecule fluorescent indicator of membrane integrity, into cells

106 domense, was recently shown to function as a fluorescent indicator of membrane potential when express

107 We used this fluorescent indicator of protein folding to evolve prote

108 nonselective membrane channels, which admits fluorescent indicators of < or = 1.5 kDa.

109 following kainate receptor activation using fluorescent indicators of [Ca2+]i and [Na+]i.

110 e, which will enable use in conjunction with fluorescent indicators of biological function.

111 ving naive, unprimed PMN in suspension using fluorescent indicators of cytoplasmic signals (Delta[Ca(

112 e recently introduced as genetically encoded fluorescent indicators of membrane voltage.

113 arly advantageous within genetically encoded fluorescent indicators of physiological signals.

114 lower dark concentration of Ca2+, we imaged fluorescent indicators of synaptic vesicle cycling and i

115 ctive, which seeks holistic consideration of fluorescent indicators, optical instrumentation, and com

116 Current methods using Na(+)-sensitive fluorescent indicators or Na(+) -sensitive electrodes ca

117 r nerve terminals filled with a low-affinity fluorescent indicator, Oregon Green BAPTA 5N.

118 Ligand probes with fluorescent indicators positioned throughout the pharmac

119 ts in analogous direction of movement of the fluorescent indicator probes.

120 consisting of serum albumins, a hydrophobic fluorescent indicator (PRODAN), and a hydrophobic additi

121 The fluorescent indicator protein for glutamate (FLIPE) cons

122 Using stably expressed fluorescent indicator proteins, we have determined for t

123 ve dye and a mitochondrial voltage-sensitive fluorescent indicator, respectively.

124 The Ca2+-sensitive fluorescent indicator rhod-2 was used to measure mitocho

125 The Ca(2+)-sensitive fluorescent indicator rhod-2 was used to monitor mitocho

126 ncoded green fluorescent protein (GFP)-based fluorescent indicators roGFP2 and HyPer, respectively.

127 hese sensors incorporate an oxygen-sensitive fluorescent indicator, Ru(II)-tris(4,7-diphenyl-1,10-phe

128 Here, resting [Na+]i was measured using the fluorescent indicator SBFI, with both traditional calibr

129 n kidney cells loaded with the Na+-sensitive fluorescent indicator SBFI.

130 V-ATPase function was assessed using the fluorescent indicators SNARF-1 and pyranine to monitor t

131 rmined using spectrophotometry employing the fluorescent indicator SYBR Gold.

132 enic mice expressing the genetically encoded fluorescent indicator synaptopHluorin in subsets of neur

133 artmentalized cAMP signaling, we constructed fluorescent indicators that report intracellular cAMP dy

134 m to create Fucci4, a set of four orthogonal fluorescent indicators that together resolve all cell cy

135 and confocal imaging of membrane-impermeant fluorescent indicators therefore represent novel approac

136 ll; and 4) anisotropic diffusion of Ca2+ and fluorescent indicator to study the evolution of Ca2+ wav

137 , these phosphors can serve as reference for fluorescent indicators to enable ratiometric intensity o

138 describe a quantitative framework for using fluorescent indicators to experimentally measure and int

139 er 6 seconds) and can be combined with other fluorescent indicators to monitor distinct cell populati

140 al approaches, including genetically encoded fluorescent indicators, ultra-thin sectioning, and live-

141 Using a fluorescent indicator, we found a subpopulation of RBCs

142 Using fluorescent indicators, we determined that, unlike in th

143 Fluorescent indicators were used to detect stimulus-evok

144 inophenol-N,N,O-triacetic acid (APTRA)-based fluorescent indicator, which displays a dissociation con

145 esidual strontium levels were monitored with fluorescent indicators, which all responded to strontium

146 n array of cross-reactive serum albumins and fluorescent indicators with chemometric analysis to diff