ライフサイエンスコーパス: fluorometry

1 reakdown of the BRB (confirmed with vitreous fluorometry).

2 ductance is demonstrated using voltage-clamp fluorometry.

3 induced intracellular Ca(2+) elevations with fluorometry.

4 by human tears was assessed by steady state fluorometry.

5 ine to 1-sulfonatoisoindole, and measured by fluorometry.

6 most relevant conformation, unlike ensemble fluorometry.

7 w color in tracheal/oropharyngeal samples by fluorometry.

8 ty was determined by way of propidium iodide fluorometry.

9 of association was measured by stopped-flow fluorometry.

10 ge) and HUVECs were used for [Ca2+]i imaging fluorometry.

11 Glutamine concentrations were measured by fluorometry.

12 ng Eu(3+)-labeled proteins and time-resolved fluorometry.

13 sion of autofluorescence in frequency-domain fluorometry.

14 binding protein (GGBP) and phase-modulation fluorometry.

15 ound suppression when using frequency-domain fluorometry.

16 e liquid chromatography and then measured by fluorometry.

17 an reconstituted thin filaments (RTFs) using fluorometry.

18 ium using frequency-domain, phase-modulation fluorometry.

19 ar pH (pHi) was measured by excitation ratio fluorometry.

20 fluorescent lifetime imaging or patch clamp fluorometry.

21 kinetics by high-resolution respirometry and fluorometry.

22 expressed P2X7Rs and performed voltage clamp fluorometry.

23 emistry, electrophysiology and voltage-clamp fluorometry.

24 site-directed mutagenesis, and voltage-clamp fluorometry.

25 structural rearrangements, using patch-clamp fluorometry.

26 changes within each VSD, using voltage-clamp fluorometry.

27 and 6)carboxyfluorescein acetoxy methylester/fluorometry.

28 led cysteines were measured by voltage clamp fluorometry.

29 of the anion channel, we used voltage clamp fluorometry.

30 onal changes were monitored by voltage clamp fluorometry.

31 mined by high-pressure liquid chromatography fluorometry.

32 and KCNQ1/KCNE1 channels using voltage clamp fluorometry.

33 f pH on K(d)(app) inferred from steady-state fluorometry.

34 ing to cells with exposed PS was measured by fluorometry after elution of bound protein.

35 Using in vitro selection techniques and fluorometry, an aptamer that binds with nanomolar affini

36 This comparison shows that for Nanodrop fluorometry, analyzing the increase of the acceptor fluo

37 -FABP) were determined by using stopped-flow fluorometry and ADIFAB, the fluorescent probe of free fa

38 nthesis in human fibroblasts was measured by fluorometry and by incorporation of radiolabeled thymidi

39 Results of fluorometry and circular dichroism (CD) spectroscopy ind

40 in conformation was confirmed by tryptophan fluorometry and circular dichroism, and was irreversible

41 SDP rapidly collapses the PMF as measured by fluorometry and flow cytometry, which triggers the slowe

42 Using fast repetition rate fluorometry and fluorescence kinetic microscopy, we show

43 living cultures and tissues based on calcium fluorometry and graph network analysis.

44 sition from mylar cards was quantified using fluorometry and hemp biomass was collected 21 post appli

45 Using voltage-clamp fluorometry and kinetic modeling, we optically track and

46 Two-photon (2P) ratiometric redox fluorometry and microscopy of pyridine nucleotide (NAD(P

47 and mitochondrial ecDNA was quantified using fluorometry and real-time PCR.

48 plied transition metal ion FRET, patch-clamp fluorometry and Rosetta modeling to measure differences

49 In experiments using voltage clamp fluorometry and simulations based on molecular dynamics

50 Here, we use voltage-clamp fluorometry and subunit concatenation to decipher the me

51 Differential scanning fluorometry and urea denaturation experiments demonstrat

52 Using voltage-clamp fluorometry and UV photolysis of intracellular caged Ca(

53 eal-time measures of in vivo phycocyanin (by fluorometry) and secchi depth was constructed to estimat

54 uranyl detection such as spectrophotometry, fluorometry, and a SERS method based on ligand-modified

55 Transcriptional analysis, fluorometry, and flow cytometry revealed evidence of sal

56 ituted cysteine accessibility, voltage clamp fluorometry, and fluorescence resonance energy transfer

57 ining transition metal ion FRET, patch-clamp fluorometry, and incorporation of a fluorescent noncanon

58 ty represents a significant challenge within fluorometry, and no effective strategy has been develope

59 A combination of fluorescence microscopy, fluorometry, and quantitative analysis demonstrated that

60 tracellular cytokine analysis, time resolved fluorometry, and RNase protection assays.

61 ng a combination of absorption spectroscopy, fluorometry, and time-correlated single photon counting.

62 elated compounds using differential scanning fluorometry- and liquid chromatography-based assays.

63 We applied a novel fast repetition rate fluorometry approach to screen genetically distinct Symb

64 g flow cytometry or multi-well culture plate fluorometry are often limited by a deficit in temporal r

65 essment using the pulse amplitude modulation fluorometry assay and chemical analysis of biologically

66 T2) with submicromolar potency in cell-based fluorometry assays and at individual synaptic vesicle cl

67 resulting DOX concentration was measured via fluorometry at 1 or 24h after FUS.

68 orescent ion, e.g. fluorescein, and off-line fluorometry, (b) loading a weakly retained ion (e.g., IO

69 We used a fluorometry-based assay of caspase activation to extend

70 cose cotransporter 1 (SGLT1) were studied by fluorometry, before and after siRNA-mediated knockdown o

71 mation of Bronsted acids in solution through fluorometry by using a convenient pK(a) probe, N(1)-aryl

72 h integrin-alpha6(+ve) hERM cells derived by fluorometry can be clonally expanded, can grow organoids

73 concentration (by enzymatic colorimetry and fluorometry); cholesteryl ester composition (by electros

74 Patch-clamp and voltage-clamp fluorometry combine spectroscopic and electrophysiologic

75 Using thioflavin T fluorometry, Congo red staining, and electron microscopy

76 a variety of methods including Thioflavin T fluorometry, Congo red staining, Thioflavin S fluorescen

77 Binding assays performed using fluorometry demonstrate that the peptide CDT binds and i

78 strength and the flexibility of patch-clamp fluorometry, demonstrating its potential as a tool for f

79 Differential scanning fluorometry (DSF), also referred to as fluorescence ther

80 This study uses patch-clamp fluorometry, electrophysiology and molecular dynamics si

81 Voltage-clamp fluorometry experiments and kinetic modeling suggest tha

82 Voltage-clamp fluorometry experiments indicate that both the finger lo

83 s of (1)H NMR, microcalorimetry, UV-vis, and fluorometry experiments.

84 can be detected by spectrophotometry (S) and fluorometry (F).

85 Although voltage-clamp fluorometry fills this gap, it is limited to sites extra

86 A new gated form of phase fluorometry for measuring lifetimes is presented.

87 The guide's main focus is on steady state fluorometry, for which available standards and instrumen

88 Since its introduction, patch-clamp fluorometry has been responsible for invaluable advances

89 mulated basophil activity by using automated fluorometry (histamine) and flow cytometry (activation m

90 ar binding measured directly by stopped-flow fluorometry implicates k(off) as a major factor for the

91 his problem, we have implemented patch-clamp fluorometry in combination with the incorporation of the

92 HCO3- buffer) and recording [Ca2+]i by ratio fluorometry in isolated cat and rat glomus cells.

93 ine activity across the striatum using fiber fluorometry in mice.

94 ing system for long-term, fast-scale calcium fluorometry in neurons.

95 2+]i and the rate of Mn2+ influx with fura-2 fluorometry in rabbit aortic smooth muscle cells in prim

96 haracterize this movement with voltage-clamp fluorometry in single-cysteine mutants.

97 was measured with pulse amplitude modulated fluorometry in thylakoids and PSII enriched membrane fra

98 l function (high-resolution respirometry and fluorometry) in gSAT and aSAT, S(I) (frequently sampled

99 king their activation by using voltage clamp fluorometry, in channels with intact voltage sensors and

100 his detection resulted in a PECL signal, and fluorometry information, including RGB values, was captu

101 Calcium fluorometry is critical to determine cell homeostasis or

102 r results reveal that excised liposome patch fluorometry is superior to traditional cell-attached MA

103 Voltage clamp fluorometry measurements combining electrophysiological

104 Amplex Red fluorometry measurements indicate that the relative cont

105 l ion channel, gramicidin, and voltage-clamp fluorometry measurements were performed with a voltage-d

106 Stopped-flow fluorometry monitoring the 2-aminopurine fluorescence de

107 assayed for cholesterol content by enzymatic fluorometry (n = 10, >70 years).

108 High-resolution respirometry and fluorometry of BAT mitochondria showed that loss of mito

109 Fluorometry of dissociated pancreatic acini, preloaded w

110 carboxyethyl)-5,6-carboxyfluorescein (BCECF) fluorometry of stably slc4a10-transfected NIH-3T3 fibrob

111 Patch-clamp fluorometry of the double- and single-insert constructs

112 Fluorometry on 1,2-dimyristoyl-sn-glycero-3-phosphocholi

113 itutes active in high-precision steady-state fluorometry performed a first comparison of fluorescence

114 Redox fluorometry provides quantitative information on the red

115 DdPCR-Tail is comparable to qPCR and fluorometry (QuBit) and allows sensitive quantification

116 cumulation using radioimmunoassay and Fluo-3 fluorometry, respectively.

117 cence analysis by pulse-amplitude modulation fluorometry revealed severe damage to photosystem II (PS

118 Time-resolved fluorometry revealed that ACBP-bound parinaroyl-CoAs had

119 Voltage-clamp fluorometry revealed that the E176K substitution alters

120 Voltage clamp fluorometry revealed that the voltage-sensing domain of

121 Voltage clamp fluorometry reveals voltage-driven rearrangements in thr

122 Voltage-clamp fluorometry showed a loss of a fast component of S4 fluo

123 Fast Repetition Rate fluorometry showed downregulated photosynthesis during a

124 Differential scanning fluorometry showed that RIG-I bound to agonists, and ant

125 sured using pulse amplitude modulation (PAM) fluorometry, showed that the optimized spectrum from the

126 However, our voltage clamp fluorometry studies indicate that these residues report

127 Results of calcium fluorometry studies indicated that V1 agonist exposure i

128 bolic activity of biofilms was determined by fluorometry study.

129 bination of electrophysiology, voltage-clamp fluorometry, synthetic BigDyn analogs, and noncanonical

130 For this purpose, we applied the patch-clamp fluorometry technique and observed correlated changes in

131 We used the voltage clamp fluorometry technique to define the role of the region p

132 In this study, we use the voltage clamp fluorometry technique to identify the molecular mechanis

133 Using a noninvasive fluorometry technique to monitor sequential turnover of

134 ng and ligand binding, using the patch-clamp fluorometry technique with a unique fluorescent cAMP ana

135 Using standard fluorometry, the limit of detection was 2.00 +/- 0.07 pM

136 of the [Ca2+]i signal in cell populations by fluorometry, the pattern of the [Ca2+]i signal in indivi

137 Finally, combining with halide-selective fluorometry, the synthetic conduit was identified as an

138 R, negative-stain TEM, differential scanning fluorometry, thermal scanning Raman spectroscopy, turbid

139 th determinations of serum retinol by direct fluorometry, this method is still a viable choice for fi

140 e microscopy, flow cytometry, or plate-based fluorometry, this system allows immediate, direct, and q

141 a, and used quantitative PCR and chlorophyll fluorometry to assess the structure and function of Symb

142 Here, we employ voltage-gated fluorometry to characterize conformational changes in th

143 We here used voltage clamp fluorometry to define how the homologous P259R mutation

144 We used voltage-clamp fluorometry to detect S4 movements and to correlate S4 m

145 ermal titration calorimetry and stopped-flow fluorometry to determine and analyze the thermodynamics

146 Here, we use voltage clamp fluorometry to determine how KCNE1 and KCNE3 affect the

147 Here, we use voltage clamp fluorometry to determine how KCNE3 affects the voltage s

148 ration was evaluated quantitatively by ratio fluorometry to determine the lumenal pH of the phagosome

149 and urea efflux was measured by stopped-flow fluorometry to determine the urea transport kinetics of

150 ve used rapid pressure jump and stopped-flow fluorometry to investigate calcium and magnesium binding

151 Here, we used voltage clamp fluorometry to investigate movements in the cysteine-ric

152 In the present study, we used voltage-clamp fluorometry to measure conformational changes in the neu

153 We used voltage-clamp fluorometry to measure protein motion at specific region

154 First, we used fluorometry to measure the doxorubicin concentrations in

155 We then used combined voltage clamp and fluorometry to monitor pentobarbital-induced channel act

156 method of Kamp et al. by using stopped-flow fluorometry to resolve flip-flop rates of both short and

157 We used voltage-clamp fluorometry to study conformational changes in human SER

158 es in voltage sensing, we used voltage-clamp fluorometry to track conformational changes of the KCNQ3

159 sfer electroporation, and used in cellulo AP fluorometry to track the movement of each Ca(V)1.1 VSD i

160 Using an optical approach (voltage-clamp fluorometry) to track the movement of the individual vol

161 electron microscopy, and H(2)O(2) assay kit fluorometry, to examine these claims.

162 mass spectrometry (charge pattern shift) and fluorometry (tryptophan fluorescence quenching).

163 Patch clamp fluorometry using a synthetic PI(4,5)P2 whose fluorescen

164 imately 2 nM) when measured by time-resolved fluorometry using CHO cell lines stably expressing CXCR1

165 Voltage clamp fluorometry (VCF) allows simultaneous measurement of vol

166 We used voltage clamp fluorometry (VCF) and molecular dynamics (MD) simulation

167 Here, we used voltage-clamp fluorometry (VCF) combined with fluorophore-quencher pai

168 In the present study, we used voltage-clamp fluorometry (VCF) to measure conformational changes in r

169 In the present study, we used voltage-clamp fluorometry (VCF) to measure simultaneously, for 5-HT(3)

170 ing cysteine accessibility and voltage clamp fluorometry (VCF).

171 absence of beta subunits using voltage-clamp fluorometry (VCF).

172 sent investigation quantitative Thioflavin T fluorometry was used on a comparative weight-to-weight b

173 Functional site-directed fluorometry was used to probe the conformational changes

174 Voltage-clamp fluorometry was used to record ion channel activity and

175 Stopped-flow fluorometry was used to study the kinetics of the reacti

176 bination with absorbance and emission matrix fluorometry, was applied to assess how agricultural land

177 retinol concentrations determined by direct fluorometry, we assayed 196 blood samples from children

178 With patch-clamp fluorometry, we confirmed that the cytoplasmic domains r

179 Using voltage clamp fluorometry, we find that the acidic pocket undergoes co

180 Using voltage clamp fluorometry, we found here that S4 in HCN channels moves

181 Using single-cell fluorometry, we found that engagement of PECAM-1 by mAbs

182 Using voltage clamp fluorometry, we found that the conformational changes in

183 Using patch-clamp fluorometry, we have investigated the calcium and voltag

184 ptimal analysis approach to use for Nanodrop fluorometry, we have performed both ensemble and single-

185 the S3-S4 region and by using voltage clamp fluorometry, we have resolved the conformational changes

186 Using voltage-clamp fluorometry, we here detect two conformational changes r

187 Using voltage-clamp fluorometry, we show that AHA incorporation permits site

188 iological and optical approach voltage-clamp fluorometry, we show that Gbetagamma acts by selectively

189 Using voltage-clamp fluorometry, we show that only VSD-III possesses kinetic

190 ned from HPLC and those obtained from direct fluorometry were significantly different in samples with

191 electrophysiology, and differential scanning fluorometry were used to characterize Na(+) and H(+) tra

192 ved this problem by performing voltage-clamp fluorometry with a fluorescent unnatural amino acid.

193 ed transition metal ion FRET and patch clamp fluorometry with a fluorescent, noncanonical amino acid

194 id and could not be resolved by stopped-flow fluorometry with a mixing time of <50 ms.

195 time fluorescent microscopy with Fluo-3 and fluorometry with Fura-2.

196 vity of the selected enzymes was analyzed by fluorometry with the aid of 4-methylumbelliferryl deriva

197 Cl-NERF, and DM-NERF, using frequency-domain fluorometry, with the objective of identifying lifetime-