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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
8 with a mixture solution of the antigen and a HRP-labeled detector antibody was used.
9 single stranded DNA reporter probe bearing a HRP molecule, followed by substrate addition and fast el
10  to evaluate the performance of CareStart, a HRP-2 based RDT, using microscopy as reference.
11 fied SPE, and then a second antibody, i.e. a HRP-labeled anti-immunoglobulin G, was deposited onto th
12 abelled common structural antibody (CSA-1-Ab-HRP) against Salmonella.
13 peroxidase (HRP) co-modified AuNPs (AuNPs/Ab-HRP).
14                      The fabricated AuNPs/Ab-HRP-amplified aptamer immunosensing SPCE strips were fur
15                            The ERalpha-MP-Ab-HRP bioconjugate formed was injected into the microFED a
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
21 when compared to conventional ELISA using an HRP labelled antibody.
22      The v-CuNWs sensor was compared with an HRP-enzyme-based biosensor showing excellent correlation
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
27 mine the binding affinity between ArtinM and HRP.
28  are labeled and quantified using biotin and HRP-conjugated streptavidin.
29 w2 CAST) with venom extracts, bromelain, and HRP was performed.
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
31  protein bridge was inserted between GOx and HRP to connect their hydration shells.
32 occurred with luminol, hydrogen peroxide and HRP enzyme, and the emission of light from the catalytic
33 in pilot tests, the biotinylated protein and HRP-labeled streptavidin for its detection.
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
36 onstrated sufficient activity of uricase and HRP at a ratio of 5U:5U and pH 7.0.
37 ed polyclonal anti-peroxidase antibody (anti-HRP-Alexa Fluor 488).
38 horseradish peroxidase-secondary antibodies (HRP-Ab2).
39 ating HA-Ag and the HRP labeled HA antibody (HRP-HA-Ab).
40                  Thus, only analyte/antibody-HRP complex will generate a signal.
41 amer and HRP linked aptamer (Au-PAMA/aptamer-HRP) as electrochemical label in the sandwich format and
42 ity, and also provides identical results, as HRP ELISA.
43              Hemin/G-quadruplex structure as HRP mimicking-DNAzyme significantly improved the catalyt
44             To conduct the biosensors assay, HRP conjugated OTA was added to the free OTA solutions a
45  immunosensor was immersed in antibody-AuNPs-HRP composites, the ECL signal greatly decreased, which
46 eradish-peroxidase-conjugated avidin (avidin-HRP).
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
49 re particles with subsaturating amounts of b-HRP and b-IgG.
50             Direct electron transfer between HRP and electrode is achieved through PNTs.
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 (
53                           BAT with bromelain/HRP showed a sensitivity of 50%/81% and a specificity of
54 murexide dye from its complex with Ni(2+) by HRP-II present in serum samples.
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
59 investigated reactions of rutin oxidation by HRP take place in a ping-pong kinetic mechanism.
60  of magnitude more sensitive than commercial HRP-based reagents.
61  The introduction of streptavidin-conjugated HRP and a simple magnetic separation allow colorimetric
62  further linked to a streptavidin-conjugated HRP reporter.
63 cteria will conjugate to their corresponding HRP-antibodies laying in wait and the immune-target meas
64                  The method offers to detect HRP-II as low as 1 pM without any interference from some
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
73  examined to provide excess epoxy groups for HRP coupling.
74 rogen peroxide was used as the substrate for HRP and then the response current (RC) could be detected
75          Colorimetric quantification of free HRP indicated that the RCEA achieved a detection limit o
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
78 hancement in activity for closely spaced GOx/HRP assemblies.
79 ten-horseradish peroxidase conjugate (hapten-HRP), which is subsequently incubated with a fluorophore
80                                        Here, HRP-avidin was substituted with the human adenosine deam
81                            In sheep with HF, HRP treatment induced progressive falls in mean arterial
82 d in an osmium based redox polymer hydrogel (HRP-Os) was physically adsorbed on Au microelectrodes fo
83              Similar to anti-ICAM, anti-ICAM-HRP was specifically internalized and transported across
84 ection was done based on the anti rabbit IgG HRP (Horseradish Peroxidase) which binds to the immune c
85                  The binding of the Anti-IgY-HRP is detected by recording the electrocatalytic signal
86 beled with horse radish peroxidase (Anti-IgY-HRP).
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
89 mbda515 nm) with the concomitant increase in HRP-II concentration in the mixture.
90 on of the glycoenzyme (typically observed in HRP) leading to bioelectrocatalytic currents up to 0.1 m
91 found in catalases, only one is operative in HRP.
92 information on the catalase-like reaction in HRP.
93 ineered through screening of 17 cut sites in HRP followed by directed evolution, reconstitute into an
94 with psoriasis had greater NCB and increased HRP prevalence than healthy volunteers.
95                                   Individual HRP molecules are trapped within surface-tethered lipid
96                                         Like HRP, DHP has been investigated as a potential bioremedia
97 es conjugated directly to enzyme labels like HRP that provide signal amplification or with nanopartic
98                      Expression of a luminal HRP-tagged syt1 construct and subsequent H2 O2 applicati
99 rticles functionalized with DNA and multiple HRP molecules.
100 utation is solely responsible for the neural HRP epitope deficiency in the nac(1) mutant.
101       Due to efficient catalytic activity of HRP mimicking-DNAzyme, the proposed immunosensor exhibit
102 ent Michaelis-Menten constant (K(M)(app)) of HRP on the nano-Ni-SnO(2) was estimated as 0.221 mM.
103 and probed the enzymatic activity changes of HRP in a catalyzed H2O2-amplex red reaction.
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
108               Additionally, a single dose of HRP resulted in an instantaneous increased incorporation
109       This proof-of-concept encapsulation of HRP through PSS nanocapsules may pave the way for altern
110 ion, which allowed several binding events of HRP-Ab2 on each nanosphere.
111 microwell, and subsequently the formation of HRP-mimicking DNAzymes was stimulated by adding hemin mo
112 e H2O2 remains, indicating the inhibition of HRP activity at high concentration of H2O2.
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
115 )-anti-TGF conjugates by covalent linkage of HRP and anti-TGF onto V-Phe-SWCNT hybrids.
116 ved by introducing the multibioconjugates of HRP-Ab2-CNSs onto the electrode surface through "sandwic
117              Using a luminescence readout of HRP activity, screening of approximately 110,000 small m
118 ransmitter release depending on the route of HRP uptake.
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%
123 +/-) cells without any significant effect on HRP uptake.
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.
133 nti-Fib labeled with horseradish peroxidase (HRP) and hydroquinone (HQ) as the redox mediator.
134 sily monitored using horseradish peroxidase (HRP) and o-dianisidine.
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
137 ay (ELISA) employing horseradish peroxidase (HRP) as the detection enzyme.
138 d catalytic cycle of horseradish peroxidase (HRP) by its substrate H2O2.
139 in antibody (Ab) and horseradish peroxidase (HRP) co-modified AuNPs (AuNPs/Ab-HRP).
140 , mouse IgG) using a horseradish peroxidase (HRP) colorimetric assay.
141 sites for subsequent horseradish peroxidase (HRP) coupling, which in turn significantly enhances elec
142  rapid dispersion of horseradish peroxidase (HRP) enzyme into the sample solution.
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
147  using a tracer with horseradish peroxidase (HRP) for the enzymatic labeling was performed.
148  using a tracer with horseradish peroxidase (HRP) for the enzymatic labeling.
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
154                      Horseradish peroxidase (HRP) is one of the most relevant peroxidase enzymes, use
155 nzymatic activity of horseradish peroxidase (HRP) is strongly inhibited by Cu(I), which can be used i
156 O2) was catalyzed by horseradish peroxidase (HRP) labeled on the secondary antibodies.
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
167 self conjugated with horseradish peroxidase (HRP) to produce a measurable signal.
168                      Horseradish peroxidase (HRP) was encapsulated by the PNT and glucose oxidase (GO
169  on the stability of horseradish peroxidase (HRP) was studied in both a short-term experiment, where
170 xidation of rutin by horseradish peroxidase (HRP) was studied.
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).
178 B) after addition of horseradish peroxidase (HRP)-conjugated anti-IgG antibodies.
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
183 ve immunoassay using horseradish peroxidase (HRP)-labeled tracers was performed.
184                      Horseradish peroxidase (HRP)-labelled cortisol is added to compete with the cort
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
188  described using the horseradish peroxidase (HRP)-mimicking DNAzyme as an amplifying label.
189 e hemin/G-quadruplex horseradish peroxidase (HRP)-mimicking DNAzyme as catalytic labels that provide
190            Using the horseradish peroxidase (HRP)-O-phenylenediamine-H2O2 electrochemical detection s
191 -conjugated Ramp and horseradish peroxidase (HRP).
192 t proteins (GFPs) or horseradish peroxidase (HRP).
193 tibody conjugated to horseradish peroxidase (HRP).
194  is then oxidized by horseradish peroxidase (HRP).
195 Ps) bearing adsorbed horseradish peroxidase (HRP).
196 te oxidase (LOX) and horseradish peroxidase (HRP).
197 lso demonstrated for horseradish peroxidase (HRP).
198 e oxidase (POx), and horseradish peroxidase (HRP).
199  electrochemistry of horseradish peroxidase (HRP)/nano-SnO(2) composite has been studied.
200 noassays, which used horseradish peroxidase (HRP, R(2) = 0.964) and fluorescein isothiocyanate (FITC,
201 nti-PSA labeled with horseradish peroxidase (HRP-labeled anti-PSA) as secondary antibody.
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
204                     Horse radish peroxidase (HRP) is one of the most common enzymes used for signal a
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.
208  hydrogen peroxide reaction with peroxidase (HRP) conjugated to the anti-NS1.
209  interest (presently horseradish peroxidase, HRP, a mannose glycoprotein) as the biochemical target f
210 or enzymatic tracer (Horseradish peroxidase--HRP).
211 n nanoparticles with horseradish peroxidise (HRP) for catalytic colorimetric assay and for streptavid
212 hosphatase (ALP) and horseradish peroxidise (HRP).
213                        Data from fluid-phase HRP electron tomography showed that fibricarriers could
214 ry plaque burden (NCB) and high-risk plaque (HRP) prevalence between patients with psoriasis (n=105),
215                The composite of AuNP-SAM-PNT/HRP-GO(x) to fabricate a sensor electrode in this study
216 n with peroxidase-labeled streptavidin (poly-HRP-Strept) polymer.
217                    Hydroxyl radical probing (HRP), which is performed routinely in many laboratories,
218  viral sequences from high-risk progressors (HRPs) and low-risk progressors (LRPs).
219 gence of mutations in high-risk progressors (HRPs) versus low-risk progressors (LRPs).
220                                  The reduced HRP can be further oxidized by hydrogen peroxide and the
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
224                             In normal sheep, HRP reduced heart rate (P<0.001) and hematocrit (P=0.019
225 0.33 versus 1.11+/-0.32, P=0.02) and similar HRP prevalence (P=0.58).
226 rt of two model cargo proteins, VSV-G and ss-HRP.
227 irus (HPV16), compared to the standard ssDNA-HRP conjugate.
228 nd a 1% SU-8 solution was found to stabilize HRP approximately 2 times more than a 34% trehalose solu
229                  SU-8 was found to stabilize HRP up to 35 times more than trehalose in the short-term
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
233 es, biotinylated Ab(2) bound to streptavidin-HRP to provide 14-16 labels per antigen was used.
234 he hybridized biotin-miRNA with streptavidin-HRP conjugates, amperometric detection at -0.20V was car
235 ted Nb or antigen was made with streptavidin-HRP.
236 with signal amplification using V-Phe-SWCNT(-HRP)-anti-TGF conjugates as carrier tags.
237 odology involved preparation of V-Phe-SWCNT(-HRP)-anti-TGF conjugates by covalent linkage of HRP and
238 eened using a horseradish-peroxidase-tagged (HRP) mouse antibody to quantify binding.
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
241  rates were significantly lower in LRPs than HRPs, especially for sets of internal branches.
242                                          The HRP conjugated Rho/CaP strongly catalyzed H2O2 oxidation
243                                          The HRP-labelled cortisol, bonded to the capture Ab, is meas
244                                          The HRP-sensor characteristics, namely sensitivity, working
245 ance (lambda515 nm/lambda482 nm) against the HRP-II concentrations.
246 ompetition between the coating HA-Ag and the HRP labeled HA antibody (HRP-HA-Ab).
247                The BSA concentration and the HRP-anti-IgG incubation had very limited influence.
248 nal method using tetramethylbenzidine as the HRP substrate.
249 quinone is oxidized into benzoquinone by the HRP/H2O2 catalytic system.
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
252 .1 microM or 38 amol were determined for the HRP-Os/AChE-ChO electrode.
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
256 none oxidized during the regeneration of the HRP label.
257  include three-fourths and one-fourth of the HRP-mimicking DNAzyme in caged, inactive configurations
258 the formation of nanowires consisting of the HRP-mimicking DNAzyme.
259     The enhanced detection capability of the HRP-Os/AChE-ChO and PB/AChE-ChO electrodes in combinatio
260                               Performing the HRP detection assay in a flow injection system using arr
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
264                  These results show that the HRP-DNA binding protein tag conjugate can be used as an
265 d to the capture Ab, is measured through the HRP enzyme and the tetramethylbenzidine (TMB) substrate
266                                    Using the HRP-O-phenylenediamine-H2O2 electrochemical detection sy
267                                 By using the HRP-scCro conjugate together with a hybrid detection pro
268                           Interestingly, the HRPs mainly drove these differences, whereas the LRPs ma
269                                         This HRP-directed tertiary structure refinement approach gene
270                                         This HRP/nano-Ni-SnO(2) film has been used for sensitive dete
271 he catalytic reduction current is related to HRP amount immobilized on the surface, which itself is r
272  epitope variant stimulations in contrast to HRPs.
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
276                                We first used HRP reactivities to identify RNAs that form extensive he
277 titative structure refinement approach using HRP measurements to drive discrete molecular dynamics si
278 complex was detected colourimetrically using HRP labelled S. typhi Ab.
279 ng mL(-1)) and 60-fold lower than when using HRP-Ab(2) in amperometric immunosensors (0.3 ng mL(-1)).
280  subsequent chemiluminescence generation via HRP-labeled antibodies.
281 r and anteromedian nucleus injections of WGA-HRP in the same animal.
282                            Injections of WGA-HRP into OPt labeled terminals bilaterally in the antero
283                            Injections of WGA-HRP into the anteromedian nucleus labeled fusiform premo
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
289               Treatment of these arrays with HRP/H2O2 causes rapid and efficient polymerization to fo
290 ustments, eBL was positively associated with HRP-IIIgG3 seropositivity (adjusted OR: 1.60; 95% CI 1.0
291                                     BAT with HRP is a good method to determine sensitivity to CCDs.
292 36IgG1-seronegative responders compared with HRP-IIIgG3-seronegative and SE36IgG1-seropositive respon
293 e presence of immuno-complex conjugated with HRP.
294 versatility (any oxidase can be coupled with HRP-based color change reaction) make our approach suita
295 h a detection antibody already modified with HRP, obtaining an 'enhanced' label.
296 aptamer-bearing reporter phage modified with HRP.
297 cycling vesicles in hippocampal neurons with HRP and subsequent treatment with hydrogen peroxide (H2
298                            The reaction with HRP has a higher rate compared with the reaction without
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

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