ライフサイエンスコーパス: chemiluminescent

1 acts with sodium sulfite and is rendered non-chemiluminescent.

2 ion of AE with sodium sulfite renders it non-chemiluminescent.

3 eaction with sodium sulfite and thus remains chemiluminescent.

4 ysis by weak base renders AE permanently non-chemiluminescent.

5 yribonucleotide probes labeled with a highly chemiluminescent acridinium ester (AE).

6 oligonucleotide probes labeled with a highly chemiluminescent acridinium ester (AE).

7 Chemiluminescent acridinium ester labels are widely used

8 e (TTAGGG)N by solution hybridization with a chemiluminescent acridinium ester oligonucleotide probe.

9 Chemiluminescent analysis did not detect the formation o

10 Calibration of the chemiluminescent assay was conducted by developing a sta

11 sensitivity, precision, and linearity of the chemiluminescent assay was verified for known numbers of

12 horseradish peroxidase the conditions of the chemiluminescent assay were varied to optimise the condi

13 ntrations were measured by radioimmunoassay, chemiluminescent assay, ELISA, or mass spectrometry.

14 Nitrate content was measured by chemiluminescent assay.

15 were varied to optimise the condition of the chemiluminescent assay.

16 sured by immunoassay and TSH was measured by chemiluminescent assay.

17 depleted preparations and a highly sensitive chemiluminescent assay; (b) followed the reaction immedi

18 lood in vitro and in vivo by using reductive chemiluminescent assays and electron paramagnetic resona

19 were assessed in enzyme immunoassays (EIAs), chemiluminescent assays, and in vitro neutralization ass

20 gy to develop multiplexed or high-throughput chemiluminescent assays.

21 The excellent correlation (R=0.985) between chemiluminescent biosensor and conventional enzyme immun

22 icates that the accurate, precise, and rapid chemiluminescent biosensor can be applied as a new metho

23 A compact portable chemiluminescent biosensor for simple, rapid, and ultras

24 The limit of detection of chemiluminescent biosensor having a wide linear dynamic

25 A chemiluminescent biosensor, developed using the differen

26 ss substrates and used to fabricate a stable chemiluminescent choline biosensor.

27 he development of a flow-through, label-free chemiluminescent (CL) immunosensor.

28 inol and 1,10-phenanthroline are widely used chemiluminescent (CL) reagents for the analysis of a wid

29 d a simple and accurate biosensor based on a chemiluminescent (CL)-lateral flow immunoassay (LFIA) me

30 vitamin B-12 plasma concentrations by using chemiluminescent competitive immunoassay and plasma conc

31 ers separately labeled with an acridan-based chemiluminescent compound and a peroxidase is reported.

32 Formation of an immunocomplex brings the chemiluminescent compound and the peroxidase into close

33 The chemiluminescent decomposition of 1,2-dioxetanones (alph

34 atase conjugate, allowing for very sensitive chemiluminescent detection ( approximately 0.1-1.0 fmol

35 fic TGF-beta + FnEDA DVD-Ig or an FnEDA mAb, chemiluminescent detection and imaging with whole-body s

36 gated to horseradish peroxidase was used for chemiluminescent detection of ligands that block the ass

37 resonance detection of nitrosyl hemoglobin, chemiluminescent detection of NO, and inhibition of plat

38 A coupled-enzyme assay method based on the chemiluminescent detection of PP(i), using ATP sulfuryla

39 beling with biotin and streptavidin-mediated chemiluminescent detection of the excised UV photoproduc

40 ted (and motorized) photomultiplier tube for chemiluminescent detection, and (c) a magnetic lens asse

41 ucigenin is most noted for its wide use as a chemiluminescent detector of superoxide anion radical (O

42 psies from chronic lesions was enhanced by a chemiluminescent dot blot hybridization, which produced

43 e endoperoxides, interlocked fluorescent and chemiluminescent dye molecules that have a squaraine chr

44 Here we have used enhanced chemiluminescent (ECL) immunoblotting as a sensitive and

45 ection at one electrode and electrogenerated chemiluminescent (ECL) reporting at the other.

46 ectrochemical detection and electrogenerated chemiluminescent (ECL) reporting.

47 ridine) were prepared as an electrogenerated chemiluminescent (ECL) tag for a sandwich-type immunoass

48 transients (i-t curves) and electrogenerated chemiluminescent (ECL) transients in an oil/water emulsi

49 n functions as a label for use in a modified chemiluminescent electromobility shift assay (EMSA), a t

50 o fluorescent (green fluorescent protein) or chemiluminescent (embryonic alkaline phosphatase) report

51 The chemiluminescent emission of the probes was significantl

52 In conclusion, we expect that ODI chemiluminescent enzyme immunoassays (CLEIAs) using a co

53 vealed with a detectability close to that of chemiluminescent enzyme labels (the limit of detection o

54 s apo(a) bound to apoB-100] were measured by chemiluminescent enzyme-linked immunoassay and commercia

55 A direct competitive chemiluminescent enzyme-linked immunosorbent assay (CL-E

56 Chemiluminescent enzyme-linked immunosorbent assay was u

57 antibodies against ruminant C. abortus in a chemiluminescent enzyme-linked immunosorbent assay.

58 assay followed by confirmatory quantitative chemiluminescent enzyme-linked immunosorbent assays.

59 h include enzyme-linked immunosorbent assay, chemiluminescent, fluoro-immunoassays, electrical detect

60 sitive and selective reaction-based tool for chemiluminescent H2S detection and quantification, the i

61 zed and shown to be a potent enhancer of the chemiluminescent horseradish peroxidase (Type VI-A)-cata

62 Using the chemiluminescent HyPerBlu assay, no yeast H2O2 productio

63 A sub-picogram sensitive chemiluminescent immunoassay (CIA) was developed for the

64 ssay, lateral flow immunoassay, polyspecific chemiluminescent immunoassay (CLIA) with a high threshol

65 25(OH)D and 1,25(OH)2D were measured using a chemiluminescent immunoassay and a radioimmunoassay, res

66 rations were measured by using a competitive chemiluminescent immunoassay at baseline and 12 mo.

67 The automated chemiluminescent immunoassay described here is sensitive

68 eveloped a sensitive, automated, competitive chemiluminescent immunoassay for the detection of 3-phen

69 The Lumipulse G TP-N chemiluminescent immunoassay is an automated system that

70 A new homogeneous chemiluminescent immunoassay method featuring the use of

71 Chemiluminescent immunoassay was directly performed on t

72 By chemiluminescent immunoassay, all APS sera samples bound

73 sayed using an automated (1.5 hour) sandwich chemiluminescent immunoassay.

74 was subsequently used to design an anti-HCV chemiluminescent immunoassay.

75 accredited laboratory methods and a standard chemiluminescent immunoassay.

76 teoblasts was demonstrated with the use of a chemiluminescent immunoassay.

77 dissection (LCM) with sensitive quantitative chemiluminescent immunoassays has broad applicability in

78 the amount of c-Fos protein was estimated by chemiluminescent immunoblot analysis.

79 ical applications including colorimetric and chemiluminescent immunoblotting, Edman-based sequencing

80 onucleotide interactions were detected using chemiluminescent labeling and a satisfactory detection l

81 ed through the use of on-chip measurement of chemiluminescent light by the CNT photodetector.

82 Accordingly, chemiluminescent light sources such as those generated b

83 hlorophenol red-beta-D-galactopyranoside), a chemiluminescent (Lumi-Gal 530), and a bioluminescent (B

84 Chemiluminescent luminophores are considered as one of t

85 re, we describe the development of the first chemiluminescent luminophores with a direct mode of NIR

86 When combined with chemiluminescent measurement of SEAP activity in the cel

87 Spectrophotometric and chemiluminescent measurements show that the deoxymyoglob

88 The chemiluminescent method based on peroxidase-catalysed ox

89 BAs by developing a quantitative nonisotopic chemiluminescent method using biotin-labeled DNA and a d

90 mine, Espline, and reference test (Architect chemiluminescent microparticle immunoassay).

91 propyltriethoxysilane-functionalized 96-well chemiluminescent microtiter plates (MTP) using 1-ethyl-3

92 A chemiluminescent microwell assay was used to detect the

93 lectron paramagnetic resonance spectroscopy, chemiluminescent nitric oxide detection, and immunoblott

94 ion electrospray mass spectroscopy (MS), and chemiluminescent nitrogen analysis.

95 in their respective DMSO stock solutions by chemiluminescent nitrogen detection (CLND)/evaporative l

96 A chemiluminescent nitrogen detector (CLND) was also used

97 ith both a short-path thermal desorber and a chemiluminescent nitrogen detector.

98 vivo, we assessed the use of LC/MS with the chemiluminescent-nitrogen detector (CLND) and a stable i

99 spirometry and FE(NO) measurements, using a chemiluminescent NO analyzer at expiratory flow rates of

100 e stain does not interfere with conventional chemiluminescent or chromogenic detection using horserad

101 ns, such as the Belousov-Zhabotinsky and the chemiluminescent Orban transformations, and photo-excita

102 s based on an energy-transfer process from a chemiluminescent precursor to a nearby emissive fluoresc

103 Hypoxia ChemiLuminescent Probe 2 (HyCL-2) responds to nitroreduc

104 been labeled with an acridinium ester as the chemiluminescent probe and secondary antibody-coated par

105 In contrast, the chemiluminescent probe coelenterazine had no significant

106 Now, a chemiluminescent probe for cathepsin B has been develope

107 [reaction: see text] A selective chemiluminescent probe for singlet oxygen has been emplo

108 A Neospora-specific chemiluminescent probe hybridized to Southern blots of a

109 ently developed hydrophobic trap-and-trigger chemiluminescent probe molecules, were orders of magnitu

110 ere made using a highly sensitive, real time chemiluminescent probe, Pholasin.

111 obed with an alkaline phosphatase-conjugated chemiluminescent probe.

112 gy will be useful for preparation of various chemiluminescent probes for numerous applications.

113 ompound SB 202190), and also fluorescent and chemiluminescent probes.

114 on of turn-ON fluorophore-tethered dioxetane chemiluminescent probes.

115 rivatives of this AE and characterized their chemiluminescent properties.

116 ssues and to develop and validate a two-site chemiluminescent quantitative enzyme-linked immunosorben

117 gen peroxide by undergoing a three-component chemiluminescent reaction between hydrogen peroxide, per

118 distinguishes two separate pathways for the chemiluminescent reaction.

119 ent of the pore scale reaction rate, using a chemiluminescent reaction.

120 However, all other chemiluminescent reactions assumed to occur according to

121 ow "trigger" chemically and enzyme-catalyzed chemiluminescent reactions with spatial and temporal con

122 These results are compared with other chemiluminescent reactions, supporting the general trend

123 emand" photon flux from chemically catalyzed chemiluminescent reactions.

124 Using an integrase assay with a chemiluminescent readout adapted to a 96-well plate form

125 as catalytic labels for the colorimetric or chemiluminescent readout of the sensing processes (the t

126 atalytic labels that provide colorimetric or chemiluminescent readout signals.

127 phosphatase-antidigoxigenin and detected via chemiluminescent readout.

128 l)dichlororuthenium(II) hexahydrate-a common chemiluminescent reagent widely used for the analysis of

129 We have made several adjustments to standard chemiluminescent reporter gene assay protocols to minimi

130 rase and Escherichia coli beta-galactosidase chemiluminescent reporter gene assays are rapid and sens

131 A highly chemiluminescent reporter molecule, acridinium ester (AE

132 -radioactive detection using fluorescent and chemiluminescent reporters.

133 inescence reaction based on the principle of chemiluminescent resonance energy transfer (CRET).

134 of the immunocomplex and the measurement of chemiluminescent signal for quantification.

135 e oxidase and peroxidase), which generated a chemiluminescent signal in the presence of glucose and l

136 Without any separation steps, a chemiluminescent signal is generated upon addition of a

137 We demonstrated a dependence of the chemiluminescent signal on MPO activity using MPO-defici

138 itted from independent hybridization-induced chemiluminescent signal probes.

139 om a 10(-)(6) dilution of normal brain (mean chemiluminescent signal, 1.3x10(5) [SD 1.1x10(4)] for vC

140 The median chemiluminescent signal-to-cutoff ratio was similar for

141 a cost-efficient approach for detecting the chemiluminescent signal.

142 ancement in the detection sensitivity of the chemiluminescent species and thus achieving a theoretica

143 ethod for measuring the relaxation time of a chemiluminescent species is also described.

144 idic mixing scheme to enhance detection of a chemiluminescent species tris(2,2'-bipyridyl)dichlororut

145 bining the use of silver nanostructures with chemiluminescent species, a technique that our laborator

146 After the blots were developed with a chemiluminescent substrate and exposed to X-ray film, th

147 e-cortisol conjugate, detected by adding the chemiluminescent substrate luminol/enhancer/hydrogen per

148 tric substrate was used and 0.1-1 pfu when a chemiluminescent substrate was used.

149 h peroxidase (HRPase)-based detection with a chemiluminescent substrate.

150 Because chemiluminescent substrates are flowed through the capil

151 Here we report two reaction-based ChemiLuminescent Sulfide Sensors, CLSS-1 and CLSS-2, wit

152 Self-illuminating, chemiluminescent systems are particularly attractive bec

153 d onto a membrane and detected with standard chemiluminescent techniques.