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1 he heightened affinity of MnO(2) NFs for the chromogenic substrate.
2 ,5'-tetramethylbenzidine (TMB) was used as a chromogenic substrate.
3 ld have to be deployed to build a fluoro- or chromogenic substrate.
4 y assaying their peroxidase activity using a chromogenic substrate.
5 with the pathogen of interest reacts with a chromogenic substrate.
6 onjugated antibody against digoxigenin and a chromogenic substrate.
7 competitive with respect to the tripeptidic chromogenic substrate.
8 amidolytic activities toward a FIXa-specific chromogenic substrate.
9 e on a monoclonal antibody and assaying with chromogenic substrate.
10 by commercially optimized assay coupled with chromogenic substrate.
11 thrombin activity that is measurable with a chromogenic substrate.
12 n 13 min using enzymatic amplification and a chromogenic substrate.
13 nd demonstrated acetylesterase activity with chromogenic substrates.
14 centration range compared with commonly used chromogenic substrates.
15 o five-fold when compared with commonly used chromogenic substrates.
16 t rely on the availability of radioactive or chromogenic substrates.
17 stantially lower levels of activity on other chromogenic substrates.
18 ability to cleave varied trypsin-susceptible chromogenic substrates.
20 lly been measured by staining cells with the chromogenic substrate 5-bromo-4-chloro-3-indolyl-beta-d-
21 blue-colony phenotype on plates containing a chromogenic substrate, 5-bromo-4-chloro-3-indolylphospha
23 ive binding studies with a thrombin-specific chromogenic substrate, a fluorescein-labeled hirudin pep
24 ermediate, meizothrombin, that has increased chromogenic substrate activity but poor clotting activit
25 egraded approximately twice as fast than the chromogenic substrate, Ala-Pro-2naphthylamide, by dipept
26 larginine p-nitroanilide (Ac-Arg-pNA) as the chromogenic substrate all indicate a cooperative binding
28 tivator was able to degrade both a synthetic chromogenic substrate and the natural substrate fibrinog
29 C may switch the enzyme specificity with the chromogenic substrates and inhibitors but not with the n
30 h a slow conformational change by tripeptide chromogenic substrates and its specific physiological su
31 or factor X, although the affinity for small chromogenic substrates and the efficiency of factor X sc
32 e EC activator did not hydrolyze a factor Xa chromogenic substrate, and recombinant tick anticoagulan
34 h overlapping specificities, enzyme-specific chromogenic substrates, and an antibody specific for act
36 X was determined to be functional by using a chromogenic substrate assay after immunoprecipitation wi
38 ine in factor VIII activity (measured with a chromogenic substrate assay) during weeks 49 through 52
41 ortCorin exhibited catalytic activity toward chromogenic substrates but failed to cleave pro-ANP, ind
43 mpetitively inhibits the hydrolysis of small chromogenic substrates by factor Xa but binds in an orie
44 d that Na(+) stimulated the cleavage rate of chromogenic substrates by FXa or GDFXa approximately 8-2
45 nly a small effect on the hydrolysis of nine chromogenic substrates carrying substitutions at P1, P2,
46 found that all FIXa derivatives cleaved the chromogenic substrate CBS 31.39 with near normal catalyt
47 The fluorogenic substrates were compared to chromogenic substrates (CENTA, nitrocefin, and imipenem)
49 strated hyperbolic, mixed-type inhibition of chromogenic substrate cleavage by factor IXa (K(I) = 88
50 d complex increased 3-fold, and the level of chromogenic substrate cleavage by factor IXa increased m
51 by the factor IXa-phospholipid complex, and chromogenic substrate cleavage by factor IXa, only in th
52 DHG did not affect factor VIIIa half-life or chromogenic substrate cleavage by factor IXa-phospholipi
53 ith the active site, as it failed to inhibit chromogenic substrate cleavage by the factor IXa-PL comp
54 n or the ability of alpha-thrombin to cleave chromogenic substrates, clot fibrinogen, or block alpha-
55 d a variation of the two-stage assay using a chromogenic substrate (COAMATIC; 19% +/- 6.9% of FVIII W
57 higher in one-stage clot (OS) assays than in chromogenic-substrate (CS) assays, whereas recombinant F
61 ody complexes on the blot are reacted with a chromogenic substrate (either 3.3'-diaminobenzidine [DAB
64 hylbenzothiazoline-6-sulfonate), is a common chromogenic substrate for peroxidase enzymes, which are
67 Here we have identified a new and effective chromogenic substrate for Tdp2 and developed a homogeneo
68 lactopyranosides, were found to be effective chromogenic substrates for an endo-alpha-N-acetyl-D-gala
69 ative micromethod that uses conventional and chromogenic substrates for the identification of medical
71 comparison, thrombin-catalyzed hydrolysis of chromogenic substrates gives greater KSIEs and more comp
72 ously by continuous measurement of parabolic chromogenic substrate hydrolysis and fluorescence-based
73 These mutations only had modest effects on chromogenic substrate hydrolysis and the kinetics of fac
75 courses of Pg activation by SK monitored by chromogenic substrate hydrolysis had initial rates (v(1)
76 s curves of Pg activation by SK monitored by chromogenic substrate hydrolysis were parabolic, with in
79 roups were also distinguishable by using the chromogenic substrates in Dade MicroScan test panels.
80 e, was assayed by the digestion of synthetic chromogenic substrates in protein-matched aliquots of ce
83 several polyanions on the hydrolysis of the chromogenic substrate L-pyroglutamyl-L-prolyl-L-arginyl-
84 rostin, a serine protease, which cleaves the chromogenic substrate (N-benzoyl-L-Ile-L-Glu-L-Gly-L-Arg
87 emperatures from 0 to 25 degrees C using the chromogenic substrate o-nitrophenyl-beta-galactoside.
88 s and products directly and does not require chromogenic substrates or lengthy chromatography, was su
89 tracts of these cells readily hydrolyzed the chromogenic substrate p-nitrophenyl-alpha-d-glucopyranos
91 effects of the cofactor on the hydrolysis of chromogenic substrates probing the interior of the catal
92 ontrary to results in amidolytic assays with chromogenic substrates, prothrombinase is resistant to i
94 l 3 enzymes have similar activity toward the chromogenic substrate S-2238, that meizothrombin and mei
95 to the active protease plasmin, cleaved the chromogenic substrate S-2251 and the natural substrate f
96 n bound to the borrelial protein cleaved the chromogenic substrate S-2251 upon conversion by urokinas
98 in a plasma clotting assay, to hydrolyze the chromogenic substrate S2366, and to undergo inhibition b
99 Kinetic analysis of these variants using chromogenic substrates showed differences in substrate s
100 with respect to their ability to cleave the chromogenic substrate Spectrozyme PCa, react with protei
101 at the A and B toxins of C. difficile cleave chromogenic substrates that have stereochemical characte
102 in; it used an enzyme-labeled antibody and a chromogenic substrate to provide an amplified visible si
107 lycosylated pseudoform for several synthetic chromogenic substrates were considerably less (33%-50%)
109 he activation was monitored by cleavage of a chromogenic substrate with newly formed plasmin, the rea
110 The chimeric mutant cleaved a FIXa-specific chromogenic substrate with normal catalytic efficiency,
111 er venom at similar rate, but it cleaved the chromogenic substrates with a Gly at the P2 positions po
112 T99Y mutant, similar to FXa, hydrolyzed the chromogenic substrates with a Gly at the P2 positions.
114 hundredth of the quantity needed for common chromogenic substrates, with an estimated bulk cost of <
115 s were seen in reactivity towards a range of chromogenic substrates, with substantial differences in
116 bitor 6 reduced V(MAX) of FXIa hydrolysis of chromogenic substrate without affecting the K(M), sugges
117 ning with a post-azo-coupling method using a chromogenic substrate (Z-arg-arg-MNA) or by a novel assa