コーパス検索結果 (left1)
通し番号をクリックするとPubMedの該当ページを表示します
1 HRP administration produced a dose-dependent decrease in
2 HRP also induced a reduction in plasma sodium concentrat
3 HRP labeled OTA was added to the antigen solutions (stan
4 HRP measurements have, to date, only been used to evalua
5 HRP were cultured in 5 mm normal glucose, 25 mm l- or d-
6 oxylated multiwall carbon nanotubes with 106 HRP labels per 100 nm gave the highest sensitivity of 19
7 higher current density (10.52 microA/cm(2); HRP detection assay) and measured diffusion coefficient
9 single stranded DNA reporter probe bearing a HRP molecule, followed by substrate addition and fast el
11 fied SPE, and then a second antibody, i.e. a HRP-labeled anti-immunoglobulin G, was deposited onto th
16 a antibody and horseradish peroxidase (MP-Ab-HRP) were used to efficiently capture ERalpha from the s
17 ruplex structure of DNAzyme yields an active HRP-like activity that catalyzes luminol to generate a c
18 rved to wrap capsids as early as 2 min after HRP addition, indicating that the envelope had recently
19 e the preparation and characterization of an HRP conjugate with scCro DNA binding protein tag and its
20 ed a unique DNA sensing platform based on an HRP-DNA binding protein tag conjugate and a hybrid ssDNA
23 rescence microscopy, and on-sensor analysis (HRP conjugated enhanced chemiluminescence-based semiquan
24 .18+/-0.33 versus 1.03+/-0.21, P=0.004), and HRP prevalence beyond traditional risk (odds ratio, 6.0;
25 d for covalent attachment of PSA-aptamer and HRP linked aptamer (Au-PAMA/aptamer-HRP) as electrochemi
26 inding affinity constants between ArtinM and HRP for each of the parameters in the immittance functio
30 ding constant (Kd) discerned for the dye and HRP-II to Ni(2+) were 1.4 x 10(-6) M(-1) and 6.8 x 10(-9
32 occurred with luminol, hydrogen peroxide and HRP enzyme, and the emission of light from the catalytic
34 ary plaque burden and NCB quantification and HRP identification, defined as low attenuation (<30 houn
35 lting from enzymatic reaction of uricase and HRP (horseradish peroxidase), which is involved in oxidi
41 amer and HRP linked aptamer (Au-PAMA/aptamer-HRP) as electrochemical label in the sandwich format and
45 immunosensor was immersed in antibody-AuNPs-HRP composites, the ECL signal greatly decreased, which
47 en peroxide (H2O2) is then reduced by avidin-HRP in the presence of TMB (3,3',5,5'-tetramethylbenzidi
48 es of biotin-horseradish-peroxidase (40KDa b-HRP) and 60 molecules of biotin-immunoglobulin-G (150KDa
51 ophotometric detection of malarial biomarker HRP-II following an indicator displacement assay has bee
52 sIgE antibodies to MUXF3 CCD, bromelain, HRP, rApi m 1, and rVes v 5 were determined, and a BAT (
55 e present in Kenya, but may be detectable by HRP-based RDT at higher parasitaemia, possibly due to th
56 Therefore, when acid oxidation followed by HRP-catalyzed enzyme oxidation was employed, shortened (
57 iocatalysis of substrate alcohol followed by HRP-catalyzed reduction of the liberated H2O2 through MW
58 reased electrocatalytic reduction of H2O2 by HRP was monitored by differential pulse voltammetry tech
61 The introduction of streptavidin-conjugated HRP and a simple magnetic separation allow colorimetric
63 cteria will conjugate to their corresponding HRP-antibodies laying in wait and the immune-target meas
65 sample volume of 20 +/- 0.06 muL and detects HRP-II within 5 min with LOD of 30 +/- 9.6 nM in a dynam
66 The immobilization of oxidoreductase enzyme HRP on the electrodes modified with OA gold nanostructur
67 assembly with horseradish peroxidase enzyme (HRP) for bioelectrochemical sensing of hydrogen peroxide
68 th psoriasis had elevated NCB and equivalent HRP prevalence as older patients with hyperlipidemia.
69 68C5-HRP ELISA and the MA-ETN63C8/MA-ETN61C1-HRP ELISA revealed a good Pearson's r (+0.974) but a poo
70 -treated AS patients with the TNF/MA-ETN68C5-HRP ELISA and the MA-ETN63C8/MA-ETN61C1-HRP ELISA reveal
71 To prevent Golgi disassembly, we expressed HRP linked to a Golgi-resident protein and acutely trigg
72 rasitemia (n=8390) and Plasmodium falciparum HRP-2 (PfHRP-2)-related antigenemia (n=6121) following v
74 rogen peroxide was used as the substrate for HRP and then the response current (RC) could be detected
76 entification of 7 tryptic glycopeptides from HRP and 16 glycopeptides from the mixture via Mascot.
77 tened, NIR-fluorescent SWCNTs resulting from HRP-catalyzed oxidation of acid-cut HiPco SWCNTs may fin
79 ten-horseradish peroxidase conjugate (hapten-HRP), which is subsequently incubated with a fluorophore
82 d in an osmium based redox polymer hydrogel (HRP-Os) was physically adsorbed on Au microelectrodes fo
84 ection was done based on the anti rabbit IgG HRP (Horseradish Peroxidase) which binds to the immune c
87 cent infection Pf histidine-rich protein-II (HRP-II) and 6NANP, Pf-vaccine candidates SE36 and 42-kDa
88 tentially 21 times higher (95% CI 5.8-74) in HRP-IIIgG3-seropositive and SE36IgG1-seronegative respon
90 on of the glycoenzyme (typically observed in HRP) leading to bioelectrocatalytic currents up to 0.1 m
93 ineered through screening of 17 cut sites in HRP followed by directed evolution, reconstitute into an
97 es conjugated directly to enzyme labels like HRP that provide signal amplification or with nanopartic
102 ent Michaelis-Menten constant (K(M)(app)) of HRP on the nano-Ni-SnO(2) was estimated as 0.221 mM.
104 re the activity of a single concentration of HRP dried and stored on paper was monitored for 61 days.
105 ed and H2O2 depended on the concentration of HRP-mimicking G-quardruplex DNAzyme formed from the bind
106 re the activity of various concentrations of HRP dried on paper were measured after 1 h, and a long-t
107 on is performed by colorimetric detection of HRP-labelled cortisol, through optical absorption at 450
111 microwell, and subsequently the formation of HRP-mimicking DNAzymes was stimulated by adding hemin mo
113 fectiveness of a solute in the inhibition of HRP activity was better related to its ability to reduce
114 b5a(+/-) Leishmania showed 50% inhibition of HRP uptake, but hemoglobin endocytosis was uninterrupted
116 ved by introducing the multibioconjugates of HRP-Ab2-CNSs onto the electrode surface through "sandwic
119 hydrogen bond network in the distal side of HRP compensates less efficiently than in catalases for t
120 a water molecule in the "wet" active site of HRP have a substantial impact on the reaction barrier, c
121 hile strong depolarization-induced uptake of HRP suppressed evoked release and augmented spontaneous
122 r rate compared with the reaction without of HRP, whereby is part of non-enzymatic reaction about 10%
124 mechanism, hydrogen peroxide first oxidizes HRP, which then oxidizes polyaniline, thus resulting in
125 ith those who developed high risk pathology (HRP), specifically dysplasia and/or adenocarcinoma.
126 )RR antagonist, ovine handle region peptide (HRP) (1, 5, and 25 mg at 90-minute intervals), both befo
127 f glycoenzymes, like horseradish peroxidase (HRP) (an elusive enzyme to immobilize via noncovalent in
128 tagged vesicles with horseradish peroxidase (HRP) - a haem-containing plant enzyme - or antibodies ag
129 of water mobility on horseradish peroxidase (HRP) activity in solutions was investigated by measuring
130 e model glycoprotein horseradish peroxidase (HRP) and a 5-glycoprotein mixture, a 2- to 31-fold incre
131 In the biosensor, horseradish peroxidase (HRP) and glucose oxidase (GOD) were electrodeposited wit
132 aining duplexes with horseradish peroxidase (HRP) and H2O2 causes rapid and efficient polymerization.
135 with cytochrome c or horseradish peroxidase (HRP) and the analytical performances were systematically
136 nti-PSA labeled with horseradish peroxidase (HRP) as secondary antibody and H(2)O(2) as the substrate
141 sites for subsequent horseradish peroxidase (HRP) coupling, which in turn significantly enhances elec
143 catalytic reaction, horseradish peroxidase (HRP) enzyme is used for catalyzing the non-fluorescent s
144 lucose oxidase (GOx)/horseradish peroxidase (HRP) enzyme pairs on specific DNA origami tiles with con
145 p ligation reaction, horseradish peroxidase (HRP) for signal amplification, and magnetic beads for th
146 ne oxidase (DOx) and horseradish peroxidase (HRP) for the detection of histamine in fish samples has
149 e, ArtinM lectin and horseradish peroxidase (HRP) glycoprotein, used here as a model for protein-carb
150 tures with entrapped horseradish peroxidase (HRP) immobilized on an array of miniature gold electrode
151 atic activity of the horseradish peroxidase (HRP) in order to achieve an improved optical lateral flo
152 himeric CFTRs with a horseradish peroxidase (HRP) in the fourth exofacial loop in either the presence
153 eaction catalyzed by horseradish peroxidase (HRP) in the presence of H2O2 is mainly a defect-consumin
155 nzymatic activity of horseradish peroxidase (HRP) is strongly inhibited by Cu(I), which can be used i
157 re then treated with horseradish peroxidase (HRP) labeled secondary antibodies to the trans-membrane
158 of the immunosensor horseradish peroxidase (HRP) labeled secondary antibodies, specifically interact
159 signal and enormous horseradish peroxidase (HRP) labeled with gold nanoparticles (AuNPs) to consume
160 bing conformation of horseradish peroxidase (HRP) molecules using our home-developed single-molecule
161 chitosan film coated horseradish peroxidase (HRP) on a multi-walled carbon nanotube (MWCNT) modified
162 s with bromelain and horseradish peroxidase (HRP) or recombinant allergen-based IgE testing can impro
163 biotin linkages, and horseradish peroxidase (HRP) reporter enzymes covalently attached to the pVIII c
164 hanging the color of horseradish peroxidase (HRP) substrate to green indicates a positive result.
165 (Ab(2)) labeled with horseradish peroxidase (HRP) to bind to IgY on the sensor and provide amplified
166 l using enzyme label horseradish peroxidase (HRP) to measure very low (<or=30 pg mL(-1)) and elevated
169 on the stability of horseradish peroxidase (HRP) was studied in both a short-term experiment, where
171 treptavidin bound to horseradish peroxidase (HRP) was successfully immobilized onto the sensor surfac
172 xidoreductase enzyme horseradish peroxidase (HRP) were evaluated to maximize incorporation of DNAN bi
173 el cargo (the enzyme horseradish peroxidase (HRP)) to anti-ICAM and separated a 1:2 antibody:enzyme c
174 e fluid phase marker horseradish peroxidase (HRP), and were observed to wrap capsids as early as 2 mi
175 dation by MnO(2) and horseradish peroxidase (HRP), derived apparent (13)C-, (2)H-, and (15)N-kinetic
176 s similar to that of horseradish peroxidase (HRP), involving a high-valent ferryl heme and two single
177 r a model analyte of horseradish peroxidase (HRP)-avidin in the dynamic range of 0.1-3.0 mug mL(-1).
179 primary antibody and horseradish peroxidase (HRP)-conjugated secondary antibody onto AgNPs-rGO modifi
180 xide sensor by using horseradish peroxidase (HRP)-immobilized conducting polymer, polyaniline (PANI).
181 Then the widely used horseradish peroxidase (HRP)-labeled antibody (anti-CEA) in immunoassays was eff
182 s was detected using horseradish peroxidase (HRP)-labeled anticytokine Abs and a visible color reagen
185 ing hybridization, a horseradish peroxidase (HRP)-labelled DNA secondary probe complementary to the a
186 ly monitored using a horseradish peroxidase (HRP)-labelled DNA secondary probe complementary to the e
187 (ssDNA) includes the horseradish peroxidase (HRP)-like DNAzyme, optimum-length linker (10-mer-length
189 e hemin/G-quadruplex horseradish peroxidase (HRP)-mimicking DNAzyme as catalytic labels that provide
200 noassays, which used horseradish peroxidase (HRP, R(2) = 0.964) and fluorescein isothiocyanate (FITC,
202 imits obtained from horse radish peroxidase (HRP) and bisphenol A assays were 12.5 ng/ml (2.84x10(-10
203 functionalized with horse radish peroxidase (HRP) based on aminopropyl triethoxy silane (APTES) and u
205 rimary antibody and Horse Radish Peroxidase (HRP) tagged secondary antibody on the surface of GCE/f-M
206 t immobilization of horse radish peroxidase (HRP), via glutaraldehyde (Glu), for deferiprone detectio
207 -pyrrole, through a horse-radish peroxidase (HRP)-activated cross-linking of the pyrrole groups.
209 interest (presently horseradish peroxidase, HRP, a mannose glycoprotein) as the biochemical target f
211 n nanoparticles with horseradish peroxidise (HRP) for catalytic colorimetric assay and for streptavid
214 ry plaque burden (NCB) and high-risk plaque (HRP) prevalence between patients with psoriasis (n=105),
221 d release and augmented spontaneous release, HRP uptake during mild activity selectively impaired evo
222 Finally, implantations of the VEGF-releasing HRP-activated alginate-g-pyrrole hydrogel system on chic
223 and Research Training in Human Reproduction (HRP); WHO; USAID; Ministry of Health, Labour and Welfare
228 nd a 1% SU-8 solution was found to stabilize HRP approximately 2 times more than a 34% trehalose solu
230 mutant receptors to react with a steptavidin-HRP-conjugated antibody was used as the basis for examin
231 ridization, a streptavidin-peroxidase (Strep-HRP) conjugate was employed as an electrochemical indica
232 Separate measurements of a standard STREP-HRP colorimetric reaction in microtiter plates of differ
234 he hybridized biotin-miRNA with streptavidin-HRP conjugates, amperometric detection at -0.20V was car
237 odology involved preparation of V-Phe-SWCNT(-HRP)-anti-TGF conjugates by covalent linkage of HRP and
239 as a carbohydrate receptive center to target HRP was successfully used to determine the binding affin
240 was hindered by viscosity changes more than HRP activity (tested in the same system) due to the high
250 and the second one using a substrate for the HRP (3 different substrates are evaluated), which produc
251 alysis of the kinetic plots, whereas for the HRP catalytic/inhibition reaction, the experimental ampe
253 rty-five patients (16%) were included in the HRP group, 31 with dysplasia (14%) and 4 with adenocarci
254 e uncover the mechanism for reduction of the HRP Compound I intermediate by H2O2 at atomic detail.
255 nt is deficient for neural expression of the HRP epitope, which consists of N-glycans with core alpha
257 include three-fourths and one-fourth of the HRP-mimicking DNAzyme in caged, inactive configurations
259 The enhanced detection capability of the HRP-Os/AChE-ChO and PB/AChE-ChO electrodes in combinatio
261 cteria on the capture layer will prevent the HRP-labeled anti-target antibodies from migrating to the
262 ression of a wild-type Gfr gene restored the HRP epitope in neural tissues, directly demonstrating th
263 lcholine (BuCh) as an internal standard, the HRP-Os/AChE-ChO and PB/AChE-ChO electrodes exhibited exc
265 d to the capture Ab, is measured through the HRP enzyme and the tetramethylbenzidine (TMB) substrate
271 he catalytic reduction current is related to HRP amount immobilized on the surface, which itself is r
273 ntrifugation in combination with transferrin-HRP/DAB ablation showed that more than half of cyt b(558
274 s as a bioremediation enzyme because, unlike HRP, it has an internal binding cavity on the distal sid
275 system consisting of combination of uricase/HRP-CdS quantum dots (QDs) for the determination of uric
277 titative structure refinement approach using HRP measurements to drive discrete molecular dynamics si
279 ng mL(-1)) and 60-fold lower than when using HRP-Ab(2) in amperometric immunosensors (0.3 ng mL(-1)).
284 a three-part nanoconjugate consisting of WGA-HRP, AuNPs, and drugs for the treatment of diaphragm par
285 germ agglutinin horse radish peroxidase (WGA-HRP) chemically conjugated to gold nanoparticles (AuNPs)
286 tinin-conjugated horseradish peroxidase (WGA-HRP) injections revealed differences in the pattern of r
287 conjugated with horseradish peroxidase (WGA-HRP) were placed in topographically different locations
288 selectively impaired evoked release, whereas HRP uptake at rest solely potentiated spontaneous releas
290 ustments, eBL was positively associated with HRP-IIIgG3 seropositivity (adjusted OR: 1.60; 95% CI 1.0
292 36IgG1-seronegative responders compared with HRP-IIIgG3-seronegative and SE36IgG1-seropositive respon
294 versatility (any oxidase can be coupled with HRP-based color change reaction) make our approach suita
297 cycling vesicles in hippocampal neurons with HRP and subsequent treatment with hydrogen peroxide (H2
299 h as blank slides or slides not treated with HRP-labeled antibody showed negative feedback effects.
300 peroxide once the PANI is standalone without HRP immobilized, showing the enzymatic reaction is requi
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。