ライフサイエンスコーパス: fluorometry

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

2 w color in tracheal/oropharyngeal samples by fluorometry.

3 ty was determined by way of propidium iodide fluorometry.

4 of association was measured by stopped-flow fluorometry.

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

6 Glutamine concentrations were measured by fluorometry.

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

8 sion of autofluorescence in frequency-domain fluorometry.

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

10 ound suppression when using frequency-domain fluorometry.

11 e liquid chromatography and then measured by fluorometry.

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

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

14 structural rearrangements, using patch-clamp fluorometry.

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

16 and 6)carboxyfluorescein acetoxy methylester/fluorometry.

17 led cysteines were measured by voltage clamp fluorometry.

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

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

20 onal changes were monitored by voltage clamp fluorometry.

21 mined by high-pressure liquid chromatography fluorometry.

22 and KCNQ1/KCNE1 channels using voltage clamp fluorometry.

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

24 by human tears was assessed by steady state fluorometry.

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

26 most relevant conformation, unlike ensemble fluorometry.

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

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

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

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

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

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

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

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

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

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

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

38 Differential scanning fluorometry and urea denaturation experiments demonstrat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

62 Voltage-clamp fluorometry experiments and kinetic modeling suggest tha

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

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

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

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

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

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

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

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

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

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

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

74 2+]i and the rate of Mn2+ influx with fura-2 fluorometry in rabbit aortic smooth muscle cells in prim

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

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

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

78 Voltage clamp fluorometry measurements combining electrophysiological

79 Amplex Red fluorometry measurements indicate that the relative cont

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

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

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

83 Fluorometry of dissociated pancreatic acini, preloaded w

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

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

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

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

88 Redox fluorometry provides quantitative information on the red

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

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

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

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

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

94 Fast Repetition Rate fluorometry showed downregulated photosynthesis during a

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

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

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

98 bolic activity of biofilms was determined by fluorometry study.

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

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

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

102 Using a noninvasive fluorometry technique to monitor sequential turnover of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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