ライフサイエンスコーパス: HRP

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 higher current density (10.52 microA/cm(2); HRP detection assay) and measured diffusion coefficient

7 ish peroxidase) bioconjugates containing 400 HRP enzyme labels, with amplified amperometric peaks dev

8 ymeric horseradish peroxidase (poly-HRP, 400 HRPs) labels to provide large signal amplification and l

9 with a mixture solution of the antigen and a HRP-labeled detector antibody was used.

10 single stranded DNA reporter probe bearing a HRP molecule, followed by substrate addition and fast el

11 cal detection of IgA antibodies using both a HRP-based sandwich type assay and label-free detection b

12 fied SPE, and then a second antibody, i.e. a HRP-labeled anti-immunoglobulin G, was deposited onto th

13 abelled common structural antibody (CSA-1-Ab-HRP) against Salmonella.

14 peroxidase (HRP) co-modified AuNPs (AuNPs/Ab-HRP).

15 The fabricated AuNPs/Ab-HRP-amplified aptamer immunosensing SPCE strips were fur

16 The ERalpha-MP-Ab-HRP bioconjugate formed was injected into the microFED a

17 a antibody and horseradish peroxidase (MP-Ab-HRP) were used to efficiently capture ERalpha from the s

18 ruplex structure of DNAzyme yields an active HRP-like activity that catalyzes luminol to generate a c

19 All HRPs have a PWWP domain at the N-terminus that binds bot

20 e the preparation and characterization of an HRP conjugate with scCro DNA binding protein tag and its

21 ed a unique DNA sensing platform based on an HRP-DNA binding protein tag conjugate and a hybrid ssDNA

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 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

29 occurred with luminol, hydrogen peroxide and HRP enzyme, and the emission of light from the catalytic

30 in pilot tests, the biotinylated protein and HRP-labeled streptavidin for its detection.

31 ary plaque burden and NCB quantification and HRP identification, defined as low attenuation (<30 houn

32 lting from enzymatic reaction of uricase and HRP (horseradish peroxidase), which is involved in oxidi

33 onstrated sufficient activity of uricase and HRP at a ratio of 5U:5U and pH 7.0.

34 ed polyclonal anti-peroxidase antibody (anti-HRP-Alexa Fluor 488).

35 nventional HRP-labeled secondary antibodies (HRP-anti-human IgG/IgM/IgA mixture).

36 ating HA-Ag and the HRP labeled HA antibody (HRP-HA-Ab).

37 Thus, only analyte/antibody-HRP complex will generate a signal.

38 amer and HRP linked aptamer (Au-PAMA/aptamer-HRP) as electrochemical label in the sandwich format and

39 ity, and also provides identical results, as HRP ELISA.

40 Hemin/G-quadruplex structure as HRP mimicking-DNAzyme significantly improved the catalyt

41 To conduct the biosensors assay, HRP conjugated OTA was added to the free OTA solutions a

42 immunosensor was immersed in antibody-AuNPs-HRP composites, the ECL signal greatly decreased, which

43 eradish-peroxidase-conjugated avidin (avidin-HRP).

44 en peroxide (H2O2) is then reduced by avidin-HRP in the presence of TMB (3,3',5,5'-tetramethylbenzidi

45 Direct electron transfer between HRP and electrode is achieved through PNTs.

46 ophotometric detection of malarial biomarker HRP-II following an indicator displacement assay has bee

47 BAT with bromelain/HRP showed a sensitivity of 50%/81% and a specificity of

48 murexide dye from its complex with Ni(2+) by HRP-II present in serum samples.

49 e present in Kenya, but may be detectable by HRP-based RDT at higher parasitaemia, possibly due to th

50 cting cancer-derived exosomes facilitated by HRP-accelerated DA polymerization and in situ PDA deposi

51 Therefore, when acid oxidation followed by HRP-catalyzed enzyme oxidation was employed, shortened (

52 iocatalysis of substrate alcohol followed by HRP-catalyzed reduction of the liberated H2O2 through MW

53 reased electrocatalytic reduction of H2O2 by HRP was monitored by differential pulse voltammetry tech

54 investigated reactions of rutin oxidation by HRP take place in a ping-pong kinetic mechanism.

55 ties for the detection of phenolic traces by HRP-based electrochemical biosensors, yet in a more stra

56 further linked to a streptavidin-conjugated HRP reporter.

57 are detected with a mixture of conventional HRP-labeled secondary antibodies (HRP-anti-human IgG/IgM

58 cteria will conjugate to their corresponding HRP-antibodies laying in wait and the immune-target meas

59 The method offers to detect HRP-II as low as 1 pM without any interference from some

60 sample volume of 20 +/- 0.06 muL and detects HRP-II within 5 min with LOD of 30 +/- 9.6 nM in a dynam

61 The immobilization of oxidoreductase enzyme HRP on the electrodes modified with OA gold nanostructur

62 assembly with horseradish peroxidase enzyme (HRP) for bioelectrochemical sensing of hydrogen peroxide

63 th psoriasis had elevated NCB and equivalent HRP prevalence as older patients with hyperlipidemia.

64 68C5-HRP ELISA and the MA-ETN63C8/MA-ETN61C1-HRP ELISA revealed a good Pearson's r (+0.974) but a poo

65 -treated AS patients with the TNF/MA-ETN68C5-HRP ELISA and the MA-ETN63C8/MA-ETN61C1-HRP ELISA reveal

66 13%) decrease in HRP activity, which exceeds HRP performance in 50 nm pore SiO(2) particles (~36% ret

67 To prevent Golgi disassembly, we expressed HRP linked to a Golgi-resident protein and acutely trigg

68 rasitemia (n=8390) and Plasmodium falciparum HRP-2 (PfHRP-2)-related antigenemia (n=6121) following v

69 examined to provide excess epoxy groups for HRP coupling.

70 rogen peroxide was used as the substrate for HRP and then the response current (RC) could be detected

71 86 mg g(-1)), retained ~82% activity of free HRP in solution and can be recycled at least five times

72 Colorimetric quantification of free HRP indicated that the RCEA achieved a detection limit o

73 entification of 7 tryptic glycopeptides from HRP and 16 glycopeptides from the mixture via Mascot.

74 tened, NIR-fluorescent SWCNTs resulting from HRP-catalyzed oxidation of acid-cut HiPco SWCNTs may fin

75 on the reaction velocity of the popular GOx-HRP cascade, particularly in the presence of a competing

76 hancement in activity for closely spaced GOx/HRP assemblies.

77 ten-horseradish peroxidase conjugate (hapten-HRP), which is subsequently incubated with a fluorophore

78 Here, HRP-avidin was substituted with the human adenosine deam

79 In sheep with HF, HRP treatment induced progressive falls in mean arterial

80 ic acid) (gamma-PGA-HEMA), generating hybrid HRP@gamma-PGA-HEMA nanoparticles (HRP@PGH NPs).

81 Similar to anti-ICAM, anti-ICAM-HRP was specifically internalized and transported across

82 ection was done based on the anti rabbit IgG HRP (Horseradish Peroxidase) which binds to the immune c

83 The binding of the Anti-IgY-HRP is detected by recording the electrocatalytic signal

84 beled with horse radish peroxidase (Anti-IgY-HRP).

85 cent infection Pf histidine-rich protein-II (HRP-II) and 6NANP, Pf-vaccine candidates SE36 and 42-kDa

86 tentially 21 times higher (95% CI 5.8-74) in HRP-IIIgG3-seropositive and SE36IgG1-seronegative respon

87 five times with a minimal (~13%) decrease in HRP activity, which exceeds HRP performance in 50 nm por

88 mbda515 nm) with the concomitant increase in HRP-II concentration in the mixture.

89 on of the glycoenzyme (typically observed in HRP) leading to bioelectrocatalytic currents up to 0.1 m

90 found in catalases, only one is operative in HRP.

91 information on the catalase-like reaction in HRP.

92 ineered through screening of 17 cut sites in HRP followed by directed evolution, reconstitute into an

93 with psoriasis had greater NCB and increased HRP prevalence than healthy volunteers.

94 Like HRP, DHP has been investigated as a potential bioremedia

95 es conjugated directly to enzyme labels like HRP that provide signal amplification or with nanopartic

96 Expression of a luminal HRP-tagged syt1 construct and subsequent H2 O2 applicati

97 rticles functionalized with DNA and multiple HRP molecules.

98 ing hybrid HRP@gamma-PGA-HEMA nanoparticles (HRP@PGH NPs).

99 -cross-linking, the resultant nanostructured HRP@PGH/GNSs sensing film was successfully applied to co

100 g the Fe-N-C SAN as a substitute for natural HRP was further verified.

101 Due to efficient catalytic activity of HRP mimicking-DNAzyme, the proposed immunosensor exhibit

102 and probed the enzymatic activity changes of HRP in a catalyzed H2O2-amplex red reaction.

103 re the activity of a single concentration of HRP dried and stored on paper was monitored for 61 days.

104 ed and H2O2 depended on the concentration of HRP-mimicking G-quardruplex DNAzyme formed from the bind

105 re the activity of various concentrations of HRP dried on paper were measured after 1 h, and a long-t

106 on is performed by colorimetric detection of HRP-labelled cortisol, through optical absorption at 450

107 Additionally, a single dose of HRP resulted in an instantaneous increased incorporation

108 microwell, and subsequently the formation of HRP-mimicking DNAzymes was stimulated by adding hemin mo

109 e H2O2 remains, indicating the inhibition of HRP activity at high concentration of H2O2.

110 fectiveness of a solute in the inhibition of HRP activity was better related to its ability to reduce

111 b5a(+/-) Leishmania showed 50% inhibition of HRP uptake, but hemoglobin endocytosis was uninterrupted

112 )-anti-TGF conjugates by covalent linkage of HRP and anti-TGF onto V-Phe-SWCNT hybrids.

113 Using a luminescence readout of HRP activity, screening of approximately 110,000 small m

114 ransmitter release depending on the route of HRP uptake.

115 hydrogen bond network in the distal side of HRP compensates less efficiently than in catalases for t

116 a water molecule in the "wet" active site of HRP have a substantial impact on the reaction barrier, c

117 hile strong depolarization-induced uptake of HRP suppressed evoked release and augmented spontaneous

118 r rate compared with the reaction without of HRP, whereby is part of non-enzymatic reaction about 10%

119 210 pmol for amperometry) and zeptomoles of HRP (45 zmol for CL and 20 zmol for amperometry); IgG wa

120 +/-) cells without any significant effect on HRP uptake.

121 ploying wt PpDyP and 29E4 variant outperform HRP based counterparts reported in the literature by 1-4

122 mechanism, hydrogen peroxide first oxidizes HRP, which then oxidizes polyaniline, thus resulting in

123 eters, including the helix reversal penalty (HRP) and the mismatch penalty (MMP).

124 )RR antagonist, ovine handle region peptide (HRP) (1, 5, and 25 mg at 90-minute intervals), both befo

125 insulin detection is based on a peroxidase (HRP)-labeled sandwich assay whereas the cortisol detecti

126 f glycoenzymes, like horseradish peroxidase (HRP) (an elusive enzyme to immobilize via noncovalent in

127 tagged vesicles with horseradish peroxidase (HRP) - a haem-containing plant enzyme - or antibodies ag

128 of water mobility on horseradish peroxidase (HRP) activity in solutions was investigated by measuring

129 e model glycoprotein horseradish peroxidase (HRP) and a 5-glycoprotein mixture, a 2- to 31-fold incre

130 In the biosensor, horseradish peroxidase (HRP) and glucose oxidase (GOD) were electrodeposited wit

131 aining duplexes with horseradish peroxidase (HRP) and H2O2 causes rapid and efficient polymerization.

132 Horseradish peroxidase (HRP) and hydrogen peroxide concentrations were directly

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 Horseradish peroxidase (HRP) as a model enzyme was co-assembled with a photo-cro

137 nti-PSA labeled with horseradish peroxidase (HRP) as secondary antibody and H(2)O(2) as the substrate

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 ne oxidase (DOx) and horseradish peroxidase (HRP) for the detection of histamine in fish samples has

145 using a tracer with horseradish peroxidase (HRP) for the enzymatic labeling was performed.

146 using a tracer with horseradish peroxidase (HRP) for the enzymatic labeling.

147 e, ArtinM lectin and horseradish peroxidase (HRP) glycoprotein, used here as a model for protein-carb

148 tures with entrapped horseradish peroxidase (HRP) immobilized on an array of miniature gold electrode

149 atic activity of the horseradish peroxidase (HRP) in order to achieve an improved optical lateral flo

150 himeric CFTRs with a horseradish peroxidase (HRP) in the fourth exofacial loop in either the presence

151 eaction catalyzed by horseradish peroxidase (HRP) in the presence of H2O2 is mainly a defect-consumin

152 avidin-conjugated to horseradish peroxidase (HRP) in the presence of luminol and H(2)O(2).

153 Horseradish peroxidase (HRP) is one of the most relevant peroxidase enzymes, use

154 nzymatic activity of horseradish peroxidase (HRP) is strongly inhibited by Cu(I), which can be used i

155 The inhibition of horseradish peroxidase (HRP) is uncompetitive for the substrate H(2)O(2) while 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 signal and enormous horseradish peroxidase (HRP) labeled with gold nanoparticles (AuNPs) to consume

159 bing conformation of horseradish peroxidase (HRP) molecules using our home-developed single-molecule

160 loaded with multiple horseradish peroxidase (HRP) molecules, recognizing the epimark in a target DNA,

161 chitosan film coated horseradish peroxidase (HRP) on a multi-walled carbon nanotube (MWCNT) modified

162 ascade also released horseradish peroxidase (HRP) pre-attached to the amplification probes, and the r

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 ch was conjugated to horseradish peroxidase (HRP) through biotin-streptavidin binding.

166 self conjugated with horseradish peroxidase (HRP) to produce a measurable signal.

167 on the stability of horseradish peroxidase (HRP) was studied in both a short-term experiment, where

168 xidation of rutin by horseradish peroxidase (HRP) was studied.

169 treptavidin bound to horseradish peroxidase (HRP) was successfully immobilized onto the sensor surfac

170 xidoreductase enzyme horseradish peroxidase (HRP) were evaluated to maximize incorporation of DNAN bi

171 e catalytic cycle of horseradish peroxidase (HRP) without the need of H(2)O(2) to be present in the s

172 el cargo (the enzyme horseradish peroxidase (HRP)) to anti-ICAM and separated a 1:2 antibody:enzyme c

173 articles (AgNPs) and horseradish peroxidase (HRP), altogether, formed the signaling probe of the prop

174 eceptor mutagenesis, horseradish peroxidase (HRP), and ascorbate peroxidase 2 (APEX-2) proximity labe

175 ious proteins (e.g., horseradish peroxidase (HRP), bovine hemoglobin, immunoglobulin G, and glucose o

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 plex of T(30)-biotin/horseradish peroxidase (HRP)-biotin/streptavidin to the poly(A) tails, and the o

179 B) after addition of horseradish peroxidase (HRP)-conjugated anti-IgG antibodies.

180 primary antibody and horseradish peroxidase (HRP)-conjugated secondary antibody onto AgNPs-rGO modifi

181 xide sensor by using horseradish peroxidase (HRP)-immobilized conducting polymer, polyaniline (PANI).

182 Then the widely used horseradish peroxidase (HRP)-labeled antibody (anti-CEA) in immunoassays was eff

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 ame level as natural horseradish peroxidase (HRP).

197 at were labeled with horseradish peroxidase (HRP).

198 e oxidase (POx), and horseradish peroxidase (HRP).

199 choring two pairs of horseradish peroxidase (HRP)/glucose oxidase (GOx) at the vertices of TDN, which

200 and conjugated with horseradish peroxidase (HRP)] onto magnetic microbeads (MBs) used as solid suppo

201 noassays, which used horseradish peroxidase (HRP, R(2) = 0.964) and fluorescein isothiocyanate (FITC,

202 ntibody labeled with horseradish peroxidase (HRP-DAb).

203 nti-PSA labeled with horseradish peroxidase (HRP-labeled anti-PSA) as secondary antibody.

204 imits obtained from horse radish peroxidase (HRP) and bisphenol A assays were 12.5 ng/ml (2.84x10(-10

205 functionalized with horse radish peroxidase (HRP) based on aminopropyl triethoxy silane (APTES) and u

206 Horse radish peroxidase (HRP) is one of the most common enzymes used for signal a

207 rimary antibody and Horse Radish Peroxidase (HRP) tagged secondary antibody on the surface of GCE/f-M

208 t immobilization of horse radish peroxidase (HRP), via glutaraldehyde (Glu), for deferiprone detectio

209 -pyrrole, through a horse-radish peroxidase (HRP)-activated cross-linking of the pyrrole groups.

210 hydrogen peroxide reaction with peroxidase (HRP) conjugated to the anti-NS1.

211 interest (presently horseradish peroxidase, HRP, a mannose glycoprotein) as the biochemical target f

212 or enzymatic tracer (Horseradish peroxidase--HRP).

213 n nanoparticles with horseradish peroxidise (HRP) for catalytic colorimetric assay and for streptavid

214 Data from fluid-phase HRP electron tomography showed that fibricarriers could

215 ry plaque burden (NCB) and high-risk plaque (HRP) prevalence between patients with psoriasis (n=105),

216 Using polymeric horseradish peroxidase (poly-HRP, 400 HRPs) labels to provide large signal amplificat

217 tavidin-poly [horse radish peroxidase] (Poly-HRP).

218 n with peroxidase-labeled streptavidin (poly-HRP-Strept) polymer.

219 viral sequences from high-risk progressors (HRPs) and low-risk progressors (LRPs).

220 gence of mutations in high-risk progressors (HRPs) versus low-risk progressors (LRPs).

221 t encapsulation of medium to large proteins (HRP, 44 kDa and beta-gal, 465 kDa) and antibodies (ca. 1

222 ongs to the family of HDGF-related proteins (HRPs) and plays an essential role in hepatocellular carc

223 The reduced HRP can be further oxidized by hydrogen peroxide and the

224 d release and augmented spontaneous release, HRP uptake during mild activity selectively impaired evo

225 Finally, implantations of the VEGF-releasing HRP-activated alginate-g-pyrrole hydrogel system on chic

226 and Research Training in Human Reproduction (HRP), and The Bill & Melinda Gates Foundation.

227 and Research Training in Human Reproduction (HRP); WHO; USAID; Ministry of Health, Labour and Welfare

228 0.33 versus 1.11+/-0.32, P=0.02) and similar HRP prevalence (P=0.58).

229 irus (HPV16), compared to the standard ssDNA-HRP conjugate.

230 nd a 1% SU-8 solution was found to stabilize HRP approximately 2 times more than a 34% trehalose solu

231 SU-8 was found to stabilize HRP up to 35 times more than trehalose in the short-term

232 conjugate of streptavidin-peroxidase (Strep-HRP) as tracer.

233 ridization, a streptavidin-peroxidase (Strep-HRP) conjugate was employed as an electrochemical indica

234 Separate measurements of a standard STREP-HRP colorimetric reaction in microtiter plates of differ

235 he hybridized biotin-miRNA with streptavidin-HRP conjugates, amperometric detection at -0.20V was car

236 ted Nb or antigen was made with streptavidin-HRP.

237 with signal amplification using V-Phe-SWCNT(-HRP)-anti-TGF conjugates as carrier tags.

238 odology involved preparation of V-Phe-SWCNT(-HRP)-anti-TGF conjugates by covalent linkage of HRP and

239 eened using a horseradish-peroxidase-tagged (HRP) mouse antibody to quantify binding.

240 as a carbohydrate receptive center to target HRP was successfully used to determine the binding affin

241 was hindered by viscosity changes more than HRP activity (tested in the same system) due to the high

242 rates were significantly lower in LRPs than HRPs, especially for sets of internal branches.

243 Furthermore, we show that HRP, when loaded in the meso-MPN particles (486 mg g(-1)

244 The HRP conjugated Rho/CaP strongly catalyzed H2O2 oxidation

245 The HRP labels catalyzed the oxidation of a dissolved redox-

246 The HRP-labelled cortisol, bonded to the capture Ab, is meas

247 The HRP-sensor characteristics, namely sensitivity, working

248 ance (lambda515 nm/lambda482 nm) against the HRP-II concentrations.

249 ompetition between the coating HA-Ag and the HRP labeled HA antibody (HRP-HA-Ab).

250 The BSA concentration and the HRP-anti-IgG incubation had very limited influence.

251 quinone is oxidized into benzoquinone by the HRP/H2O2 catalytic system.

252 and the second one using a substrate for the HRP (3 different substrates are evaluated), which produc

253 alysis of the kinetic plots, whereas for the HRP catalytic/inhibition reaction, the experimental ampe

254 nd is suggested to provoke a decrease of the HRP as experimentally observed.

255 e uncover the mechanism for reduction of the HRP Compound I intermediate by H2O2 at atomic detail.

256 none oxidized during the regeneration of the HRP label.

257 ht signal resulting from the reaction of the HRP-labelled anti-human IgA with a H(2)O(2)/luminol/enha

258 the formation of nanowires consisting of the HRP-mimicking DNAzyme.

259 eaction of tetramethylbenzidine (TMB) on the HRP by providing a blue precipitate on the surface.

260 a 125-fold increase in sensitivity over the HRP labeled sandwich vertical flow assay.

261 Performing the HRP detection assay in a flow injection system using arr

262 cteria on the capture layer will prevent the HRP-labeled anti-target antibodies from migrating to the

263 These results show that the HRP-DNA binding protein tag conjugate can be used as an

264 d to the capture Ab, is measured through the HRP enzyme and the tetramethylbenzidine (TMB) substrate

265 Using the HRP-O-phenylenediamine-H2O2 electrochemical detection sy

266 By using the HRP-scCro conjugate together with a hybrid detection pro

267 While the HRP decreases upon decreasing the number of chiral side

268 Interestingly, the HRPs mainly drove these differences, whereas the LRPs ma

269 Then HRP@PGH NPs and graphene oxide nanosheets (GO NSs) were

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 titative structure refinement approach using HRP measurements to drive discrete molecular dynamics si

277 subsequent chemiluminescence generation via HRP-labeled antibodies.

278 r and anteromedian nucleus injections of WGA-HRP in the same animal.

279 Injections of WGA-HRP into OPt labeled terminals bilaterally in the antero

280 Injections of WGA-HRP into the anteromedian nucleus labeled fusiform premo

281 a three-part nanoconjugate consisting of WGA-HRP, AuNPs, and drugs for the treatment of diaphragm par

282 germ agglutinin horse radish peroxidase (WGA-HRP) chemically conjugated to gold nanoparticles (AuNPs)

283 tinin-conjugated horseradish peroxidase (WGA-HRP) injections revealed differences in the pattern of r

284 conjugated with horseradish peroxidase (WGA-HRP) were placed in topographically different locations

285 s, studied with the transneuronal tracer WGA-HRP, are intermixed in the binocular zone of albinos, wi

286 selectively impaired evoked release, whereas HRP uptake at rest solely potentiated spontaneous releas

287 Treatment of these arrays with HRP/H2O2 causes rapid and efficient polymerization to fo

288 ustments, eBL was positively associated with HRP-IIIgG3 seropositivity (adjusted OR: 1.60; 95% CI 1.0

289 BAT with HRP is a good method to determine sensitivity to CCDs.

290 36IgG1-seronegative responders compared with HRP-IIIgG3-seronegative and SE36IgG1-seropositive respon

291 xes and secondary antibodies conjugated with HRP onto the surface of magnetic beads.

292 versatility (any oxidase can be coupled with HRP-based color change reaction) make our approach suita

293 ctrode modified with TiO(2) impregnated with HRP.

294 of ROS on titania which, in interaction with HRP, initiate the electrocatalysis toward phenolic compo

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