1 Caspase-3
fluorometric activity assays as well as immunoblot analy
2 ADCC was determined by using a
fluorometric ADCC assay, before and after removal of pla
3 Western blot and
fluorometric analyses indicated the loss of two differen
4 Histochemical and
fluorometric analyses of GUS expression revealed that th
5 ted by delayed recovery of dsDNA analyzed by
fluorometric analysis of DNA unwinding and the more exte
6 d from DNA single-strand lesions measured by
fluorometric analysis of DNA unwinding.
7 ecules, the embryos were lysed gently, and a
fluorometric analysis of their contents was performed.
8 Fluorometric analysis using the mitochondrial probes non
9 Using
fluorometric and biochemical assays, we studied Cas9/gui
10 Supporting the quantitative
fluorometric and colorimetric assays, size exclusion chr
11 Both these
fluorometric and colorimetric methods have been successf
12 Phagocytosis was assayed by
fluorometric and colorimetric techniques.
13 ytes were identified by absorbance patterns,
fluorometric and electrochemical detection. and comparis
14 n in G-buffer into single filaments based on
fluorometric and EM observations.
15 tion FRET experiments and protein microarray
fluorometric and FRET assays.
16 omocysteine and folate were measured by HPLC-
fluorometric and microbiological methods, respectively.
17 roxide (H(2)O(2)) production was measured by
fluorometric and polarographic methods.
18 In comparison with other
fluorometric and spectrophotometric assays for the detec
19 d) of an ODS II Spherisorb column, with both
fluorometric and spectrophotometric detection.
20 A flow
fluorometric approach to study cationic lipoid-DNA compl
21 ease ATP upon mechanical stimulation using a
fluorometric approach.
22 gen peroxide production was observed both by
fluorometric as well as by SECM measurements.
23 e activity of MazFSa, including a continuous
fluorometric assay and a gel-based cleavage assay.
24 reverse transcriptase was determined using a
fluorometric assay and a poly(A) homopolymer as a templa
25 were screened for MMP-9 inhibitors, using a
fluorometric assay and gelatin zymography.
26 Fluorometric assay and zymography showed that adhesives
27 ecular Probes, Eugene, OR) was measured by a
fluorometric assay at 485 nm excitation and 530 nm emiss
28 e describes a simple, inexpensive, and rapid
fluorometric assay based on the ability of dendrimers to
29 nts in serum samples were determined using a
fluorometric assay based on the dye 6-carboxyfluoroscein
30 recombinant human PLTP were studied using a
fluorometric assay based on the excimer fluorescence of
31 A
fluorometric assay based upon the enzymatic transphospho
32 ccumulation of NADH, demonstrating that this
fluorometric assay effectively monitors calcium-dependen
33 more sensitive than the currently available
fluorometric assay for enzyme activity.
34 rophicum homologue (MthK) and a stopped-flow
fluorometric assay for fast channel activation, we show
35 We present a continuous-read,
fluorometric assay for high-throughput analysis of gluta
36 A rapid enzymatic
fluorometric assay for measuring D-arabinitol in serum w
37 A
fluorometric assay for mitochondrial membrane potential
38 The first direct and continuous
fluorometric assay for monoamine oxidase B (MAO B) has b
39 A continuous,
fluorometric assay for pectin methylesterase (PME) activ
40 We have developed a novel HPLC-based
fluorometric assay for serine hydroxymethyltransferase a
41 A continuous
fluorometric assay for tryptophan hydroxylase activity b
42 ase activity is not detectable by a standard
fluorometric assay in C3H/HeOuJ (C3H) mice homozygous fo
43 Using a
fluorometric assay in conjunction with solubilized recep
44 The
fluorometric assay is carried out at an excitation wavel
45 RP1 clusters was tested in a receptor-ligand
fluorometric assay made by immobilizing soluble LRP1 "mi
46 and bacillus viability as determined using a
fluorometric assay of bacterial viability and CFU determ
47 idase IV (DPPIV) activity was quantified via
fluorometric assay of whole vessel homogenate.
48 This paper describes an in vitro
fluorometric assay system for protein splicing based on
49 CPP32-like activity directly in an in vitro
fluorometric assay system, although z-DEVD-fmk showed mu
50 purified protein was monitored by a coupled
fluorometric assay that employed purified protoporphyrin
51 uantum dots (QDs) have been used in a simple
fluorometric assay to detect single cells of the pathoge
52 ese concerns, employing a direct, cell-based
fluorometric assay to investigate the regulation of TACE
53 ng CO2 flux across membranes, we developed a
fluorometric assay to measure CO2 entry into vesicles.
54 We used an automated enzymatic
fluorometric assay to measure serum DA/creatinine ratios
55 A
fluorometric assay using nitrate reductase and the NADPH
56 to NA inhibitors (NAIs) was evaluated with a
fluorometric assay using the 2'-(4-methylumbelliferyl)-a
57 A cell-based
fluorometric assay was used to measure intracellular Ca(
58 A
fluorometric assay was used to study WRN helicase kineti
59 ent of VWF-A2 (FRETS-VWF73) as determined by
fluorometric assay, and enhanced cleavage of ultralarge
60 -like protease activity was measured using a
fluorometric assay, and for the in situ detection of cas
61 ycin and Zn(II) was calculated using a novel
fluorometric assay, and NMR was used to identify the bin
62 o internalize anti-CA19.9 antibodies using a
fluorometric assay, and xenografts of the same lines wer
63 olipase A2 (sPLA2) activity, measured with a
fluorometric assay, is low at birth, but increases progr
64 Using a
fluorometric assay, it was determined that zopolrestat,
65 Using
fluorometric assay, the detection limit (DL) for As (III
66 (PARP) proteolysis and a specific caspase-3
fluorometric assay, was inhibited by ischemic preconditi
67 m mobilization studies were done utilizing a
fluorometric assay.
68 Caspase-9 activity was assessed by a
fluorometric assay.
69 oAlert Mitochondrial kit, and caspase 9 by a
fluorometric assay.
70 d its antioxidant capacity was measured in a
fluorometric assay.
71 Ca2+]i in response to E2 was determined in a
fluorometric assay.
72 ical impedance spectroscopy (EIS) as well as
fluorometric assay.
73 Total MMP activity was determined using a
fluorometric assay.
74 y of caspase-3, -8, or -9 was measured using
fluorometric assay.
75 erol levels were determined using a standard
fluorometric assay.
76 transcription assays and (b) by quantitative
fluorometric assays and direct microscopic observation o
77 Fluorometric assays and RT-PCR analysis of alpha1(I) col
78 Immunoblot analysis and
fluorometric assays revealed that the extents of IR-indu
79 rthern analysis, gelatin-gel zymography, and
fluorometric assays were performed on day 7 to determine
80 erized by steady-state, presteady-state, and
fluorometric assays.
81 able to that of the best currently available
fluorometric assays.
82 proliferation and chemotaxis, using specific
fluorometric assays; and 3) gene expression, using pathw
83 ssessed by measuring nitrate/nitrite using a
fluorometric-
based assay, iNOS expression was examined b
84 Using the novel
fluorometric-
based kinetic (real-time) RT-PCR, we determ
85 By traditional and
fluorometric-
based kinetic reverse transcription-PCR and
86 Here we present a
fluorometric bioassay for TF-antigen (galactose-beta-(1-
87 A new approach for the design of a
fluorometric biosensor for continuous monitoring of gluc
88 First, Fura-2
fluorometric Ca(2+) analysis shows the ability of PIP(3)
89 levels were determined by both a cell-based
fluorometric Ca(2+) assay and a ratiometric Ca(2+) imagi
90 Based on
fluorometric [
Ca(2+)]i measurements, clemizole exhibits
91 isqualate, and 3,5-dihydroxyphenylglycine in
fluorometric Ca2+ assays 3- to 6-fold, with EC50 values
92 gonist activity, with an IC50 of 3 microM in
fluorometric Ca2+ assays, whereas the analog 3,3'-dichlo
93 In the
fluorometric calcium assay, CDPPB exhibited an EC50 valu
94 Fluorometric calcium imaging and whole cell patch clamp
95 ion of whole-cell patch-clamp recordings and
fluorometric calcium imaging, we characterized calcium t
96 Fluorometric calcium measurements also show that these d
97 In addition,
fluorometric calcium measurements from retinal axon term
98 Fluorometric calcium measurements have revealed presynap
99 Fluorometric calcium measurements revealed that forskoli
100 Fluorometric calcium measurements revealed that this syn
101 lorimetric card was compared to the previous
fluorometric card for identification of yeast.
102 An analysis of caspase activity, using
fluorometric caspase assays and Western blots, indicated
103 ing for possible interactions between NM and
fluorometric/
colorimetric dyes and, most importantly, th
104 ity of NM altering the optical properties of
fluorometric/
colorimetric probes that are used to measur
105 Using a
fluorometric coupled enzyme assay and smooth muscle myos
106 Ds) capped with thioglycolic acid (TGA) as a
fluorometric Cyt c nanosensor.
107 describes the integration of laser-scanning
fluorometric cytometry and nonseparation ligand-binding
108 The use of appropriate
fluorometric derivatization procedures is of considerabl
109 to deployment in the developing world, where
fluorometric detection is more problematic.
110 nsor with regard to its applicability in the
fluorometric detection of Cyt c.
111 ment and validation of a RP-HPLC method with
fluorometric detection of derivatized isosteviol, formed
112 as been synthesized for the colorimetric and
fluorometric detection of highly competitive H2S and cya
113 INOS activity was measured by
fluorometric detection of NO.
114 e determination of these compounds, with the
fluorometric detection providing substantially greater s
115 nce liquid chromatography (HPLC) method with
fluorometric detection was developed for the routine det
116 Several methods for rapid sequestration,
fluorometric detection, and the subsequent mass spectros
117 For
fluorometric detection, the excitation and emission wave
118 labeled anti-phosphotyrosine antibody with a
fluorometric detection.
119 rocedure, based on enzymatic degradation and
fluorometric detection.
120 ols, and lanthanides do not interfere in the
fluorometric detection.
121 milar to the detection limit obtained with a
fluorometric detector when using the CNTs.
122 eport a graphene oxide (GO) nanosheets-based
fluorometric DNA biosensor to study the type and locatio
123 es and approaches the sensitivity of typical
fluorometric ELISAs.
124 hat obtained by using commercially available
fluorometric-
enzymatic assay and liquid chromatography/m
125 For
fluorometric enzyme assay (FA) 1 (FA-1), 2'-(4-methylumb
126 An easy-to-perform
fluorometric enzyme immunocapture assay (FEIA) was devel
127 ellular adhesion molecules were evaluated by
fluorometric enzyme-linked immunosorbent assay.
128 mononucleotide and NAD in milk by means of a
fluorometric,
enzyme-coupled assay.
129 A shipboard
fluorometric flow analyzer has been developed for near-r
130 With a
fluorometric flow injection analysis system harnessed to
131 ed plants was monitored using histochemical,
fluorometric GUS activity and fluorescence microscopy.
132 beled with 2-aminobenzamide, and analyzed by
fluorometric,
high-performance liquid chromatography (HP
133 We developed and applied a high throughput
Fluorometric Imaging Plate Reader (FLIPR) assay to monit
134 n to potentiate acetylcholine (ACh) in an M1
fluorometric imaging plate reader (FLIPR) functional ass
135 An automated signaling assay device, the
fluorometric imaging plate reader (FLIPR), can simultane
136 agonists were further characterized using a
fluorometric imaging plate reader assay.
137 riments on rat basophilic leukemia cells and
fluorometric imaging plate reader intracellular Ca(2+) a
138 Fluorometric imaging plate reader membrane potential dye
139 and rat recombinant P2X(7) cell lines using
fluorometric imaging plate reader technology.
140 measurements of intracellular pH on a FLIPR (
fluorometric imaging plate reader).
141 measurements of intracellular pH on a FLIPR (
fluorometric imaging plate reader).
142 n elevation of [Ca(2+)](i), measured using a
fluorometric imaging plate reader.
143 Fluorometric imaging revealed that postsynaptic depolari
144 ed sample handling, and simultaneous 96-well
fluorometric imaging to develop a high-throughput assay
145 Fluorometric imaging-based pharmacological characterizat
146 A simple
fluorometric immunological method in combination with a
147 We used a simple
fluorometric in vitro assay to determine clotting activi
148 attonella marina has been examined using the
fluorometric indicator alamarBlue.
149 ge (IC50 = 1.0-1.3 microM), as determined by
fluorometric intracellular free Ca(2+) concentration ([C
150 MP-9, MMP-12, and MMP-13 were assessed using
fluorometric kits.
151 or fluorescence under UV lights (GFPUV) as a
fluorometric marker and transformed Rickettsia typhi wit
152 ra-2 and mounted in superfusion chambers for
fluorometric measurement of [Ca2+]i.
153 epithelial barrier function was assessed by
fluorometric measurement of carboxyfluorescein uptake.
154 Tear clearance was assessed by
fluorometric measurement of collected tear fluid 15 minu
155 and compared with NHE3 activity evaluated by
fluorometric measurement of intracellular pH.
156 duces lipid headgroup order, as detected via
fluorometric measurement of intramembrane electric field
157 reas higher sensitivities were obtained from
fluorometric measurements down into sub-micromolar conce
158 he presence or absence of these agents using
fluorometric measurements of intracellular Ca2+ concentr
159 Fluorometric measurements of iodide influx in Fischer ra
160 Fluorometric measurements on these cells using a fluores
161 re content was determined using quantitative
fluorometric measurements.
162 rometry (r=0.630; n=853) and by an enzymatic-
fluorometric method (triacylglycerol) (r=0.611; n=842).
163 In addition, a less sensitive
fluorometric method exists that employs nonpeptidyl amin
164 A
fluorometric method for evaluation of activities of lipo
165 rformance liquid chromatography (HPLC)-based
fluorometric method for measuring serine hydroxymethyltr
166 We developed a microplate-based
fluorometric method for the concurrent determination of
167 The present paper describes an enzymatic-
fluorometric method for the determination of cholesterol
168 A
fluorometric method for the determination of hydroperoxi
169 We have developed a one-step
fluorometric method for the measurement of monoamine oxi
170 VICAM AflaTest and OchraTest immunoaffinity
fluorometric method in a total of 50 meat products (25 e
171 Application of the immunoaffinity
fluorometric method is an accurate, safe and rapid metho
172 The
fluorometric method is based on the reaction of ammonium
173 This
fluorometric method is based on the use of the fatty aci
174 enzyme was used to develop a fixed endpoint
fluorometric method to analyze UDP-GlcNAc.
175 Here, we report a
fluorometric method to measure carboxypeptidase activiti
176 The
fluorometric method using 2, 3-diaminonaphthalene as the
177 A
fluorometric method was utilized to determine the dissoc
178 on were used to assess H2O2 formation: (1) a
fluorometric method with emission at 590 nm, (2) an opti
179 d the mutant enzymes were compared using the
fluorometric method.
180 se data are comparable to that obtained by a
fluorometric method.
181 tamine was quantified by a glass fiber-based
fluorometric method; passive HR-IgE-stripped donor basop
182 We discuss
fluorometric methods for imaging or quantifying platinum
183 e report the development of colorimetric and
fluorometric methods for the reliable quantitation of S-
184 2+ release and Ca2+ entry were measured with
fluorometric methods in Chinese hamster ovary cells expr
185 This review article discusses these
fluorometric methods.
186 ed by up to 50%, as measured by quantitative
fluorometric microscopy (QFM) of ezrin, indicating that
187 sociated fluorescence was quantified using a
fluorometric microvolume assay technology (FMAT) scanner
188 escence-linked immunosorbent assay utilizing
fluorometric microvolume assay technology (FMAT).
189 ogeneous bead-based immunoassay for use with
fluorometric microvolume assay technology (FMAT).
190 Using the novel
fluorometric NO detection system, 4,5-Diaminofluorescein
191 This allowed for the development of a
fluorometric noncoupled assay that is 2 orders of magnit
192 In addition, the stability of the
fluorometric oligonucleotides precludes the substrate va
193 g NH4(+)-OPA product was quantified by using
fluorometric or spectrophotometric detection.
194 a trans full-length VP4 cleavage assay and a
fluorometric peptide cleavage assay.
195 e 384-well and 1536-well microplates using a
fluorometric plate reader for detection.
196 n be accomplished with a simple, inexpensive
fluorometric plate reader.
197 e of caspase activation was determined using
fluorometric profiling and the caspase inhibitor Z-Val-A
198 eTag molecules, which have the same
fluorometric property, but distinct charge-to-mass ratio
199 re studied using western blot analysis and a
fluorometric protease activity assay in the presence or
200 nhibition of protein splicing by zinc ion, a
fluorometric protein splicing assay was developed in whi
201 n analysis by a factor of 50-100 relative to
fluorometric qPCR readout.
202 -specific fluorescent label, fura-2, and its
fluorometric quantification.
203 Fluorometric quantitation of EB was performed 1 or 2 h l
204 Fluorometric quantitation of EB was performed 1 or 2 h l
205 ures for the determination of other relevant
fluorometric quantities including fluorescence quantum y
206 oximately five cycles compared to commercial
fluorometric readout.
207 sed on this observation, we have developed a
fluorometric,
real-time assay that is adapted to a multi
208 Here, we used a
fluorometric RNAP molecular beacon assay to discern part
209 tor (L1) exhibits selective colorimetric and
fluorometric sensing of Zn(2+) in aqueous medium at pH 7
210 MOFs with widely varied
fluorometric sensing properties have been developed usin
211 ent and state of the art of colorimetric and
fluorometric sensor arrays.
212 yzed using UV-visible spectrophotometric and
fluorometric stopped-flow techniques.
213 Fluorometric studies demonstrated that LPS in vivo signi
214 Fluorometric studies demonstrated that LPS in vivo signi
215 Fluorometric studies link TNF's acid-enhanced membrane i
216 sterase 1 enzyme activity measured using the
fluorometric substrate 4-methylumbelliferyl-6-thiopalmit
217 nts using an activity-based immunosassay and
fluorometric substrate assay.
218 Enzymatic analysis with
fluorometric substrates showed that caspase 2, 3, and 9
219 well with data obtained by a solution-phase
fluorometric technique using a porous membrane diffusion
220 was quantified using an enzyme-coupled NADH
fluorometric technique, regulatory myosin light chain (r
221 osylated proteins were quantitated using the
fluorometric technique.
222 d its enzymatic activity was determined by a
fluorometric technique.
223 dynamic data obtained using fluorimetric and
fluorometric techniques in conjunction with fluorescence
224 with various retinoids were characterized by
fluorometric titration and photoaffinity labeling.
225 Fluorometric titration revealed that typical DNA stainin
226 essions for analyzing spectrophotometric and
fluorometric titrations are applicable to all fluorescen
227 ty distributions for Pb(II) binding, whereas
fluorometric titrations are explained by monomodal distr
228 ty constants (K(obs)) measured by UV-vis and
fluorometric titrations at variable pH for esters of 4,5
229 +) (K(d) = 0.3 micrometer), as determined by
fluorometric titrations of the recombinant protein.
230 The methods employed are potentiometric and
fluorometric titrations, fluorescence excitation-emissio
231 lues determined under the same conditions by
fluorometric titrations.
232 Findings were confirmed with a
fluorometric TRAP assay in which fluorescent primers spe
233 antly according to hemolysis grade; however,
fluorometric values did.
234 We have devised a highly sensitive
fluorometric well plate assay for tissue transglutaminas