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1 difluoro-4-methylumbelliferyl phosphate as a fluorogenic substrate.
2 5) value of 342 microM were obtained for the fluorogenic substrate.
3 red for maximal enzymatic activity against a fluorogenic substrate.
4 sured in transduced cells and media, using a fluorogenic substrate.
5 bstrate poly(ADP-ribose) polymerase and of a fluorogenic substrate.
6 ta-galactosidase through its activation of a fluorogenic substrate.
7 low micromolar inhibitory potency against a fluorogenic substrate.
8 in as the enzyme and BODIPY FL casein as the fluorogenic substrate.
9 focal fluorescence microscopy using a Bodipy fluorogenic substrate.
10 ivities of KLK5 and KLK7 were compared using fluorogenic substrates.
11 r aminopeptidase activity against many model fluorogenic substrates.
12 cted and quantitated by flow cytometry using fluorogenic substrates.
13 eactions is often limited by the need to use fluorogenic substrates.
14 human sirtuin hydrolases against a panel of fluorogenic substrates.
15 igher chymotrypsin-like activity measured on fluorogenic substrates.
16 the cleavage of macromolecular and synthetic fluorogenic substrates.
17 caspase-12 when incorporated into synthetic fluorogenic substrates.
18 iety of intracellular enzymes with available fluorogenic substrates.
19 ratio at a given analyte concentration with fluorogenic substrates.
20 inatorial substrate libraries and individual fluorogenic substrates.
21 cPLA2 showed 20-fold higher activity toward fluorogenic substrates, 1-O-(1-pyrenedecyl)-2-arachidono
22 ing enzyme (IDE)-catalyzed hydrolysis of the fluorogenic substrate 2-aminobenzoyl-GGFLRKHGQ-ethylened
23 parameters for the interaction of E with the fluorogenic substrate 2-aminobenzoyl-Thr-Ile-Nle-Phe(p-N
24 ntained heat-labile sialidase activity for a fluorogenic substrate, 2'-(4-methylumbelliferyl)-alpha-D
25 g the lysophosphatidylcholine-like substrate fluorogenic substrate 3 (FS-3) and approximately 10,000
26 te specificity of human Sulf-1 employing the fluorogenic substrate 4-methylumbelliferyl sulfate (4-MU
27 fluorescent compounds seen with the existing fluorogenic substrate, 4-methylumbelliferyl-alpha-D-gluc
28 analysis of xylanase activity using a novel fluorogenic substrate, 6,8-difluoro-4-methylumbelliferyl
29 e assay measures the rate of hydrolysis of a fluorogenic substrate-6,8-difluoro-4-methylumbelliferyl
30 atalytic specificity was determined with the fluorogenic substrate: 6-carboxyfluorescein approximatel
31 the rat theta 2-2 enzyme (rGSTT2-2) with the fluorogenic substrate 7-amino-4-chloromethyl coumarin (C
32 e H(2)O(2)-supported oxidation of the marker fluorogenic substrate 7-ethoxy-4-trifluoromethylcoumarin
33 iluted 20000-fold into buffer containing the fluorogenic substrate 9H-(1,3-dichloro-9,9-dimethylacrid
34 continuously monitored using a validated MMP fluorogenic substrate, a microdialysis system placed wit
35 ctions of Staphylococcus aureus sortase with fluorogenic substrate Abz-LPETG-Dnp in the presence or a
37 reening of a library of 137,180 tetrapeptide fluorogenic substrates against the T. brucei 20 S protea
40 d with a solution containing glucose and the fluorogenic substrate amplex red through the engineered
42 f dextran sulphate (DXS)-stimulation using a fluorogenic substrate and capillary immunoassays to quan
43 ndividual reaction vessels containing excess fluorogenic substrate and catalyzed the production of a
44 centrates, procoagulant lipid vesicles and a fluorogenic substrate and triggered with tissue factor (
46 Di- and tetra-oligopeptides were used as fluorogenic substrates and irreversible/competitive inhi
47 e expression were assessed by using specific fluorogenic substrates and macroarrays, respectively.
49 ghlight possible limitations associated with fluorogenic substrates and Ubl activity-based probes and
50 to detect the production of thrombin using a fluorogenic substrate, and (iv) titration of argatroban
51 al-Try-7 amino-4 methyl coumarin, a specific fluorogenic substrate, and Cbz-Leu-Leu-Tyr-CHN2, a speci
52 cs of several commonly used FRET substrates, fluorogenic substrates, and six of the 11 reported SARS-
53 Values of k(cat)/K(M) with hypersensitive fluorogenic substrates are 10(4) and 10(2)-fold lower th
56 e compared with pro-memapsin 2 using two new fluorogenic substrates, Arg-Glu(5-[(2-aminoethyl)amino]n
58 rance of peptidase activity that cleaved the fluorogenic substrates Asp-Glu-Val-Asp-aminotrifluoromet
59 ity was monitored in cells after PDT using a fluorogenic substrate, (Asp-Glu-Val-Asp)-AFC (7-amino-4-
64 tral enzyme of this network, by developing a fluorogenic substrate-based method for time- and space-r
65 like activity as assessed by the cleavage of fluorogenic substrate benzyloxycarbonyl-DEVD-7-amido-4-(
66 .02 s-1 for the enzymatic hydrolysis of this fluorogenic substrate by FIV PR under the conditions of
67 ress curves of the hydrolysis of a sensitive fluorogenic substrate by FXIa in the presence of PN-2 to
69 : see text]-galactosidase activity using the fluorogenic substrate, C[Formula: see text]FDG; and auto
70 The strategy utilized in the design of this fluorogenic substrate can be applied in future endeavors
75 ate cleavage pattern of human AMCase against fluorogenic substrates, chitobiose-4-methylumbelliferyl
81 tivity, as measured in cell lysates with the fluorogenic substrate DEVD-AMC, was elevated almost imme
82 In this work, we report readily synthesized fluorogenic substrates enabling enzyme-economical evalua
83 this paper, we describe the development of a fluorogenic substrate for 17beta-hydroxysteroid-dehydrog
85 ge of DEVD-aminomethylcoumarin (DEVD-AMC), a fluorogenic substrate for caspases 2, 3, and 7; in contr
87 using pH-sensitive fluorescent probes and a fluorogenic substrate for cysteine proteases showed that
88 no, 4-methyl coumarin amide (AAMCA), a novel fluorogenic substrate for FAAH, was designed and synthes
92 plication of a novel type of chromogenic and fluorogenic substrate for protease detection is describe
94 cein di-beta-d-galactopyranoside, which is a fluorogenic substrate for the intracellular enzyme beta-
96 the identification and characterization of a fluorogenic substrate for tumor necrosis factor-alpha co
97 re assayed with a novel, membrane-impermeant fluorogenic substrate for vp165, we found that insulin s
98 ethylrhodamine) have been used previously as fluorogenic substrates for a number of DNA modifying enz
99 r enzyme fluorescence (REF) that uses custom fluorogenic substrates for bacterial enzymes allows rapi
100 k through development of near-infrared (NIR) fluorogenic substrates for beta-lactamase, an enzyme exp
104 ort the rational design of the near-infrared fluorogenic substrates for human GzmA and mouse GzmA.
105 bes a design of cell-permeable near-infrared fluorogenic substrates for imaging beta-lactamase expres
106 or engineering highly specific and sensitive fluorogenic substrates for target conjugative enzyme(s),
108 ully developed colorectal neoplasia-specific fluorogenic substrates, highlighting the ED substrate as
109 plarily demonstrated for the cleavage of the fluorogenic substrate hydrodabcyl-Ser-Phe-EDANS by the p
111 ating and neighboring cells using orthogonal fluorogenic substrates in various mixed cell systems.
112 reaction to convert a novel, cell-permeable fluorogenic substrate into fluorescein within living cel
118 tered the interaction of the enzyme with the fluorogenic substrate (Leu-Arg-Gly-Gly-NH)2-rhodamine.
119 agents led to the cleavage of the caspase-4 fluorogenic substrate, LEVD-7-amino-4-trifluoromethylcou
121 ty was assayed by monitoring cleavage of the fluorogenic substrate Mca-RPPGFSAFK(Dnp)-OH, a derivativ
123 ochemistry, immunoblots, and cleavage of the fluorogenic substrate N-benzyloxycarbonyl-Asp-Glu-Val-As
124 ghly sensitive, selective, and tight binding fluorogenic substrate of a copper amine oxidase that is
128 ity of rat nardilysin was investigated using fluorogenic substrates of the type 2-aminobenzoyl-GGX(1)
129 culture by introducing a combination of two fluorogenic substrates or a fluorogenic and a luminogeni
130 ty was comparable with results obtained with fluorogenic substrates or fluorochrome-labeled inhibitor
134 (Danio rerio) CYP1 isoforms with a series of fluorogenic substrate probes was determined by the rate
135 6 kDa proteolytic fragments with a synthetic fluorogenic substrate produced hyperbolic substrate vers
136 le Michael or Diels-Alder reactions of these fluorogenic substrates provide products of significantly
137 e in fluorescence on caspase cleavage of the fluorogenic substrates ranged from 40 to 83 depending on
140 Ti(2) and i(2)ANDNOTi(1) gates that cleave a fluorogenic substrate, reporting through an increase in
141 cs an i(1)ANDi(2) gate and cleaves the other fluorogenic substrate, reporting through an increase in
142 trates are required in costly amounts, while fluorogenic substrates require an additional apparatus (
143 ts, containing varying concentrations of the fluorogenic substrate resorufin beta-d-galactopyranoside
144 el in human plasma, employing ecarin and the fluorogenic substrate, resulted in improvement of the de
145 ave combined the GzB substrate with a second fluorogenic substrate selective for caspase 3 to allow b
146 the TF.factor VIIa (FVIIa) complex toward a fluorogenic substrate showed that the catalytic efficien
155 ed components are mixed with an enzyme and a fluorogenic substrate that permits to follow the enzymat
157 compounds should provide a diverse range of fluorogenic substrates that may be used to rapidly scree
158 A large proportion of studies relies on fluorogenic substrates that mimic the chemical propertie
162 n droplet microfluidic screening systems use fluorogenic substrates to measure enzymatic activities w
163 Mildly permeabilized cells were exposed to fluorogenic substrates to monitor the activity of intrac
164 low micromolar range) in competition with a fluorogenic substrate toward a recombinant form of the t
166 ded MBL)) and the identification of suitable fluorogenic substrates (umbelliferone-derived cephalospo
168 hancement of precision and sensitivity using fluorogenic substrates was demonstrated in a direct-bind
176 or the variants were determined with a novel fluorogenic substrate, which was designed to match the n
177 generation of fluorescent molecules from the fluorogenic substrate with the assistance of Fe(3)O(4) n
178 ANG cleaves a dinucleotide version of the fluorogenic substrates with a k(cat)/K(M) value of 61 M(
179 analysis of a series of otherwise identical fluorogenic substrates with Lys at P1 and different resi
181 ge by purified mutant enzymes of a series of fluorogenic substrates with systematic changes in P(4) a
182 ently monitored with peptidic chromogenic or fluorogenic substrates, with certain peptide sequences i
183 ot protect monocytes from apoptosis, and the fluorogenic substrate YVAD-AFC failed to show an increas
185 latin zymography in SDS-PAGE, and by in situ fluorogenic substrate zymography in RPE/choroid sections