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 rations and distributions, and without using fluorescent indicators.

9 of conventional biosensing methods, such as fluorescent indicators.

10 nderstanding their functions using synthetic fluorescent indicators.

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

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

13 s by use of different commercially available fluorescent indicators.

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

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

16 transcriptionally linked genetically encoded fluorescent indicators (2-in-1-GEFIs) for multiparametri

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

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

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

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

21 Using fluorescent indicators, action potential duration, Ca2+

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

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

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

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

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

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

28 nce imaging, due to development of sensitive fluorescent indicators and observation of spatiotemporal

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

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

31 urements in water; colorimetric changes of a fluorescent indicator; and chemical shift changes for hi

32 to visualize cellular membrane voltages with fluorescent indicators are an attractive complement to t

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

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

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

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

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

38 ications of a new class of voltage-sensitive fluorescent indicators built on a modified carbofluoresc

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

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

41 We have dubbed these fluorescent indicators 'cameleons'.

42 Using impermeant fluorescent indicators, capacitance measurements and ele

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

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

45 ar copper, we demonstrate with a ratiometric fluorescent indicator, crisp-17, that cytosolic Cu(I) le

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

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

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

49 ve an imprinted library, followed by in situ fluorescent indicator displacement analysis.

50 ctive indicator displacement assays (eIDAs), fluorescent indicator displacement assays (FIDAs), react

51 For this, a new fluorescent indicator displacement method was developed.

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

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

54 2+)](i)) as revealed by simultaneous DIC and fluorescent indicator dye microscopy.

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

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

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

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

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

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

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

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

63 s, it can be applied across model organisms, fluorescent indicators, experimental modes, and imaging

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

65 etric, highly responsive genetically encoded fluorescent indicators, FiNad, for monitoring NAD(+) dyn

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

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

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

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

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

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

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

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

74 , we developed a genetically encoded far-red fluorescent indicator for monitoring synaptic Zn(2+) dyn

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

76 Our engineered far-red fluorescent indicator for synaptic Zn(2+) (FRISZ) displa

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

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

79 Fluorescent indicators for Ca(2+) ions revolutionized ou

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

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

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

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

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

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

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

87 Recently developed fluorescent indicators for voltage largely report change

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

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

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

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

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

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

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

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

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

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

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

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

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

101 Functional imaging using fluorescent indicators has revolutionized biology, but a

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

103 Although fluorescent indicators have been broadly utilized for mo

104 Applications as fluorescent indicators in rat hippocampal neurons includ

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

106 2+]i) was measured at 35 degrees C using the fluorescent indicator indo-1 in patch-clamped, single ut

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

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

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

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

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

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

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

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

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

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

117 3R), have generally used 45Ca2+-flux assays, fluorescent indicators loaded within either the cytosol

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

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

120 n in living cells, here we synthesized a new fluorescent indicator, mitoferrofluor (MFF).

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

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

123 Two fluorescent indicators, namely, Calcofluor white and Con

124 activity as assessed by quantification of a fluorescent indicator of caspase-1 activity (FAM-FLICA [

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

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

127 We utilized a photostable and bright fluorescent indicator of glutamate release (iGluSnFR3) t

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

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

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

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

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

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

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

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

136 We discuss advances in fluorescent indicators of neural activity, viral and gen

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

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

139 d semiconductor quantum dots serve as bright fluorescent indicators of the TF-DNA bound (on bead) and

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

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

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

143 Ligand probes with fluorescent indicators positioned throughout the pharmac

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

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

146 The fluorescent indicator protein for glutamate (FLIPE) cons

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

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

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

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

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

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

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

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

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

156 rmined using spectrophotometry employing the fluorescent indicator SYBR Gold.

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

158 ple mixed a Cy5-cassette with a pyrene-based fluorescent indicator that responded to changes in Cu(2+

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

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

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

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

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

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

165 bstacles by implementing genetically-encoded fluorescent indicators to monitor both glutamate and GAB

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

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

168 Targeting small-molecule fluorescent indicators using genetically encoded protein

169 introduce a new platform for 'chemigenetic' fluorescent indicators, utilizing the self-labeling Halo

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

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

172 Fluorescent indicators were used to detect stimulus-evok

173 This study discloses a fluorescent indicator which can address both.

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

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

176 evolution produced JEDI-1P, a green-emitting fluorescent indicator with enhanced performance across a

177 ed and sensitivity of chemically synthesized fluorescent indicators with cell-type specific genetic m

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

179 applied to wild-type and genetically encoded fluorescent indicator zebrafish lines.