ライフサイエンスコーパス: horseradish peroxidase

1 the bi-enzymatic system (glucose oxidase and horseradish peroxidase).

2 tes were filled intracellularly in vivo with horseradish peroxidase.

3 tric output upon conjugation to streptavidin-horseradish peroxidase.

4 d using a secondary anti-IgG conjugated with horseradish peroxidase.

5 eptide-derived tyrosyl radicals, formed from horseradish peroxidase.

6 le components, such as hydrogen peroxide and horseradish peroxidase.

7 r several weeks by the plant-derived enzyme, horseradish peroxidase.

8 radical cation (compound I) intermediates of horseradish peroxidase.

9 viously reported for nitric oxide binding to horseradish peroxidase.

10 polymerized by biocatalysis with laccase or horseradish peroxidase.

11 dyes, antibodies against synaptotagmin-1, or horseradish peroxidase.

12 t(s) in the absence of hydrogen peroxide and horseradish peroxidase.

13 ed using wheat germ agglutinin conjugated to horseradish peroxidase.

14 cific enzyme models such as chymotrypsin and horseradish peroxidase.

15 biotin used in conjunction with streptavidin-horseradish peroxidase.

16 Wheat germ agglutinin-horseradish peroxidase (0.5-1.0 mul) was injected into t

17 rs [ionic conductance (G), mannitol, 182 Da; horseradish peroxidase, 40 kDa] and gliadin peptides [33

18 About 200 molecules of biotin-horseradish-peroxidase (40KDa b-HRP) and 60 molecules of

19 aspartate and/or glutamic acid residues into horseradish peroxidase, a plant enzyme that exhibits ess

20 possible to identify peptides that bound to horseradish peroxidase, alkaline phosphatase, and beta-g

21 ng the solvent-accessible carboxyl groups of horseradish peroxidase and alkaline phosphatase, with di

22 Model proteins, horseradish peroxidase and alpha1-acid glycoproteins, we

23 lly regulates the fluid-phase endocytosis of horseradish peroxidase and also specifically induced the

24 noassay based on the competition of atrazine-horseradish peroxidase and atrazine was established with

25 d subjected them to enzymatic oxidation with horseradish peroxidase and concluded that the analytical

26 a myoblogin, hemoglobin I, heme oxygenase 1, horseradish peroxidase and cytochrome c oxidase were cal

27 These cells were retrogradely labeled with horseradish peroxidase and examined in retinal whole mou

28 The cells were retrogradely labeled with horseradish peroxidase and examined in retinal wholemoun

29 By reporting the encapsulation of horseradish peroxidase and firefly luciferase, we demons

30 The treatment of these arrays with horseradish peroxidase and H(2)O(2) resulted in oxidativ

31 )O(2), and nitrite anion (NO(2)(-)) and with horseradish peroxidase and H(2)O(2).

32 to the DNA were prepared by the reaction of horseradish peroxidase and H2O2 with DNA having the appr

33 d by mixing the polymer solutions containing horseradish peroxidase and hydrogen peroxide.

34 al, increased secretion of reporter proteins horseradish peroxidase and lipase at least 50% in small-

35 (H(2)O(2)) based on the co-immobilization of horseradish peroxidase and methylene blue on the functio

36 Based on superposition of the horseradish peroxidase and myeloperoxidase structures, t

37 The enzyme cocktail (glucose oxidase, horseradish peroxidase and potassium ferrocyanide as med

38 that some proteins with peroxidase activity (horseradish peroxidase and prostaglandin hydroperoxidase

39 Peptide nanotubes (PNTs) encapsulating horseradish peroxidase and surface coated with acetylcho

40 > 200 MHz are important to stabilization of horseradish peroxidase and yeast alcohol dehydrogenase i

41 ediate between that of a typical peroxidase (horseradish peroxidase) and a typical globin (horse hear

42 t types of enzymes (superoxide dismutase and horseradish peroxidase), and a fluorescent dye (fluoresc

43 ound molecules: 60 superoxide dismutase, 120 horseradish peroxidase, and 20 fluorescein molecules on

44 damage, hepatocyte damage, ileal leakage of horseradish peroxidase, and bacterial translocation comp

45 conclude that the ferryl forms of myoglobin, horseradish peroxidase, and cytochrome c peroxidase are

46 s were labeled with cholera toxin-conjugated horseradish peroxidase, and dendritic arbors were recons

47 e were labeled with cholera toxin-conjugated horseradish peroxidase, and dendritic arbors were recons

48 by an enzymatic assay using glucose oxidase, horseradish peroxidase, and ferrocyanide as electron-tra

49 e layers is compared with that of protamine, horseradish peroxidase, and inactivated catalase.

50 ve soil enzymes (C. fumago chloroperoxidase, horseradish peroxidase, and laccase from T. versicolor).

51 Anterograde transport of horseradish peroxidase applied to the olfactory epitheli

52 Cu(B) in cytochrome c oxidase and Arg 38 in horseradish peroxidase are not corrected, the pK(a) calc

53 reaction carried out by glucose oxidase and horseradish peroxidase as a model system, here we study

54 alyzed using diacetyldeuteroheme-substituted horseradish peroxidase as a trapping agent for both O-2.

55 say to detect C-reactive protein (CRP) using horseradish peroxidase as the enzyme label.

56 oxygen species production was measured by a horseradish peroxidase assay.

57 Glucose oxidase and horseradish peroxidase can be contained in these structu

58 Yet, the intricacies of the horseradish peroxidase-catalyzed oxidation of the reduct

59 is used with a H2O2 destruction catalyst and horseradish peroxidase-catalyzed oxidation of thiamine t

60 benzidine) (PDB), is then carried out by the horseradish peroxidase-catalyzed polymerization of 3,3'-

61 e of this mixing technique by initiating the horseradish peroxidase-catalyzed reaction between hydrog

62 tion of 3,3'-diaminobenzidine by endocytosed horseradish peroxidase, causing an increase in the vesic

63 immunoassay (FI) platform was developed with horseradish peroxidase chemiluminescence as the reporter

64 e microscopy and by electron microscopy with horseradish peroxidase colloidal gold to label lysosomes

65 retrograde tracer (wheat-germ agglutinin apo-horseradish peroxidase colloidal gold) with labeling of

66 this is amplified by an avidin/biotinylated horseradish peroxidase complex.

67 hybridoma cells are incubated with a hapten-horseradish peroxidase conjugate (hapten-HRP), which is

68 er brief incubations with an anti-biotin IgG-horseradish peroxidase conjugate and a precipitable hors

69 An antifluorescein-horseradish peroxidase conjugate binds to either a fluor

70 then developed by binding of a streptavidin-horseradish peroxidase conjugate followed by incubation

71 aled by the introduction of the streptavidin-horseradish peroxidase conjugate that catalytically conv

72 s green fluorescent protein and streptavidin-horseradish peroxidase conjugate.

73 acer wheat germ agglutinin-apo (inactivated) horseradish peroxidase conjugated to colloidal gold, or

74 s of wheat germ agglutinin-apo (inactivated) horseradish peroxidase conjugated to colloidal gold, or

75 Horseradish peroxidase-conjugated antibody binds to the

76 he SCN showed no anterograde labeling with a horseradish peroxidase-conjugated cholera toxin B (CT-HR

77 uminol-based chemiluminescence for detecting horseradish peroxidase-conjugated cotinine, we employed

78 ated with anti-Nrf2 primary and biotinylated-horseradish peroxidase-conjugated secondary antibody, af

79 Horseradish peroxidase-conjugated streptavidin was used

80 et biomolecules, which then allow binding of horseradish-peroxidase-conjugated avidin (avidin-HRP).

81 Moreover, streptavidin-horseradish peroxidase conjugates in conjunction with a

82 Furthermore, two transganglionic tracers, horseradish peroxidase conjugates of cholera toxin B sub

83 ecifically labeling cleared tissues based on horseradish peroxidase conversion of diaminobenzidine to

84 e of different amines, a glycine oxidase and horseradish peroxidase coupled assay was developed.

85 Horseradish peroxidase cross-linked in an osmium based r

86 Cholera toxin B conjugated to horseradish peroxidase (CTB-HRP) was injected into the g

87 anglionic tracer, cholera toxin beta-subunit-horseradish peroxidase (CTb-HRP), into wall of various g

88 structures of the ferryl forms of myoglobin, horseradish peroxidase, cytochrome c peroxidase, and cat

89 h enzyme-linked immunosorbent assay (ELISA), horseradish peroxidase direct ELISA, and bicinchoninic a

90 neurons and thalamic afferents labeled with horseradish peroxidase during intracellular recordings i

91 amine (OA) synthesis and their assembly with horseradish peroxidase enzyme (HRP) for bioelectrochemic

92 The reactivities of TAML activators and the horseradish peroxidase enzyme are critically compared.

93 ly used DNA nano-barcodes, quantum dots, and horseradish peroxidase enzyme to detect multiple protein

94 orporated IC was analyzed using a simplified horseradish peroxidase enzyme-based colorimetric scheme

95 yme electrode is made of alcohol oxidase and horseradish peroxidase enzymes immobilized on to a carbo

96 NCS broke down by human myeloperoxidase and horseradish peroxidase enzymes, revealing that incidenta

97 ution, identifying new mutants of the enzyme horseradish peroxidase exhibiting catalytic rates more t

98 gic processes were found in close contact to horseradish peroxidase-filled fSR profiles, no morpholog

99 ction of elevated serum levels of the tracer horseradish peroxidase following rectal administration.

100 obtained by measuring AhpC competition with horseradish peroxidase for hydrogen peroxide; this value

101 ent with peroxygenase activity reported with horseradish peroxidase for the hydroxylation of phenol.

102 covered with a film containing myoglobin or horseradish peroxidase grown in alternating layers with

103 Horseradish peroxidase has been demonstrated to catalyze

104 Its application to horseradish peroxidase has resulted in enzyme variants u

105 g in series (trehalase, glucose oxidase, and horseradish peroxidase) have been coimmobilized in calci

106 es and a bacterial protein conjugated with a horseradish peroxidase homopolymer (ProtA-HRP40).

107 t docking and "wiring" of glycoenzymes, like horseradish peroxidase (HRP) (an elusive enzyme to immob

108 o examine this link, we tagged vesicles with horseradish peroxidase (HRP) - a haem-containing plant e

109 The effect of water mobility on horseradish peroxidase (HRP) activity in solutions was i

110 For the model glycoprotein horseradish peroxidase (HRP) and a 5-glycoprotein mixtur

111 In the biosensor, horseradish peroxidase (HRP) and glucose oxidase (GOD) w

112 of the SNS- and ANi-containing duplexes with horseradish peroxidase (HRP) and H2O2 causes rapid and e

113 ompetitive assay using anti-Fib labeled with horseradish peroxidase (HRP) and hydroquinone (HQ) as th

114 gen peroxide which is easily monitored using horseradish peroxidase (HRP) and o-dianisidine.

115 Oxidation of SCN-, Br-, and Cl- (X-) by horseradish peroxidase (HRP) and other plant and fungal

116 preferred-null axis defined was stained with horseradish peroxidase (HRP) and prepared for electron m

117 ss fiber inserts either with cytochrome c or horseradish peroxidase (HRP) and the analytical performa

118 Although oxidations of aromatic amines by horseradish peroxidase (HRP) are well-known, typical ali

119 mplex immunoassay with anti-PSA labeled with horseradish peroxidase (HRP) as secondary antibody and H

120 linked immunosorbent assay (ELISA) employing horseradish peroxidase (HRP) as the detection enzyme.

121 2)O(2) electrochemical detection scheme with horseradish peroxidase (HRP) as the enzyme label.

122 er of ferrocenylalkanethiol and encapsulated horseradish peroxidase (HRP) at a gold electrode for amp

123 We report here that incubation of horseradish peroxidase (HRP) at acidic pH with H(2)O(2)

124 ion of the redox-mediated catalytic cycle of horseradish peroxidase (HRP) by its substrate H2O2.

125 To test the hypothesis that horseradish peroxidase (HRP) can be inactivated by pheno

126 molecules of anti-thrombin antibody (Ab) and horseradish peroxidase (HRP) co-modified AuNPs (AuNPs/Ab

127 del target protein (i.e., mouse IgG) using a horseradish peroxidase (HRP) colorimetric assay.

128 rials provides numerous sites for subsequent horseradish peroxidase (HRP) coupling, which in turn sig

129 ces fluid convection and rapid dispersion of horseradish peroxidase (HRP) enzyme into the sample solu

130 In the catalytic reaction, horseradish peroxidase (HRP) enzyme is used for catalyzi

131 we organized discrete glucose oxidase (GOx)/horseradish peroxidase (HRP) enzyme pairs on specific DN

132 (PEG) hydrogel spheres containing the enzyme horseradish peroxidase (HRP) for application as optical

133 the use of a specific gap ligation reaction, horseradish peroxidase (HRP) for signal amplification, a

134 iosensor employing diamine oxidase (DOx) and horseradish peroxidase (HRP) for the detection of histam

135 competitive immunoassay using a tracer with horseradish peroxidase (HRP) for the enzymatic labeling

136 direct competitive assay using a tracer with horseradish peroxidase (HRP) for the enzymatic labeling.

137 plex red (AR) by H(2)O(2) in the presence of horseradish peroxidase (HRP) gives rise to an intensely

138 interactions, for example, ArtinM lectin and horseradish peroxidase (HRP) glycoprotein, used here as

139 Horseradish peroxidase (HRP) has been the subject of int

140 d of hydrogel microstructures with entrapped horseradish peroxidase (HRP) immobilized on an array of

141 mbination with the enzymatic activity of the horseradish peroxidase (HRP) in order to achieve an impr

142 E41o(-)) by expressing chimeric CFTRs with a horseradish peroxidase (HRP) in the fourth exofacial loo

143 new evidence that the reaction catalyzed by horseradish peroxidase (HRP) in the presence of H2O2 is

144 To test this hypothesis, I injected horseradish peroxidase (HRP) into the ventral horn unila

145 Horseradish peroxidase (HRP) is one of the most relevant

146 The enzymatic activity of horseradish peroxidase (HRP) is strongly inhibited by Cu

147 In this work, picosecond dynamics of horseradish peroxidase (HRP) isoenzyme C in the free for

148 nd hydrogen peroxide (H2O2) was catalyzed by horseradish peroxidase (HRP) labeled on the secondary an

149 These were then treated with horseradish peroxidase (HRP) labeled secondary antibodie

150 l signal and sensitivity of the immunosensor horseradish peroxidase (HRP) labeled secondary antibodie

151 ots to enhance the basal signal and enormous horseradish peroxidase (HRP) labeled with gold nanoparti

152 as attained by using bioconjugates featuring horseradish peroxidase (HRP) labels and secondary antibo

153 By perturbing conformation of horseradish peroxidase (HRP) molecules using our home-de

154 Many individual horseradish peroxidase (HRP) molecules were isolated and

155 ase (FcAOx) and sol-gel chitosan film coated horseradish peroxidase (HRP) on a multi-walled carbon na

156 th both venoms as well as with bromelain and horseradish peroxidase (HRP) or recombinant allergen-bas

157 ers attached via avidin-biotin linkages, and horseradish peroxidase (HRP) reporter enzymes covalently

158 Changing the color of horseradish peroxidase (HRP) substrate to green indicate

159 en secondary antibodies (Ab(2)) labeled with horseradish peroxidase (HRP) to bind to IgY on the senso

160 wich immunoassay protocol using enzyme label horseradish peroxidase (HRP) to measure very low (<or=30

161 rresponding antibody, itself conjugated with horseradish peroxidase (HRP) to produce a measurable sig

162 he enantioselectivity of yeast surface-bound horseradish peroxidase (HRP) toward chiral phenols has b

163 Horseradish peroxidase (HRP) typically oxidizes aniline

164 an affinity-purified antibody to biotin with horseradish peroxidase (HRP) using cyanuric chloride (CC

165 Characterization of bound horseradish peroxidase (HRP) was carried out using a rea

166 Horseradish peroxidase (HRP) was conjugated to colloidal

167 Horseradish peroxidase (HRP) was encapsulated by the PNT

168 Seven days later horseradish peroxidase (HRP) was injected into the body

169 oxy novolac resin (SU-8) on the stability of horseradish peroxidase (HRP) was studied in both a short

170 mechanism of enzymatic oxidation of rutin by horseradish peroxidase (HRP) was studied.

171 The model protein streptavidin bound to horseradish peroxidase (HRP) was successfully immobilize

172 Horseradish peroxidase (HRP) was used as label on detect

173 luding chicken ovalbumin, bovine fetuin, and horseradish peroxidase (HRP) were digested by Pronase, p

174 and the extracellular oxidoreductase enzyme horseradish peroxidase (HRP) were evaluated to maximize

175 were imaged at light (FM1-43) and electron (horseradish peroxidase (HRP)) levels over stimulus frequ

176 inally, we coupled a model cargo (the enzyme horseradish peroxidase (HRP)) to anti-ICAM and separated

177 Horseradish peroxidase (HRP), a plant enzyme, also oxidi

178 ules were labelled by the fluid phase marker horseradish peroxidase (HRP), and were observed to wrap

179 The uptake of horseradish peroxidase (HRP), applied as an extracellula

180 The heme of hemoproteins, as exemplified by horseradish peroxidase (HRP), can undergo additions at t

181 ment factors for the oxidation by MnO(2) and horseradish peroxidase (HRP), derived apparent (13)C-, (

182 catalytic cycle of DHP is similar to that of horseradish peroxidase (HRP), involving a high-valent fe

183 We used horseradish peroxidase (HRP), Lucifer yellow, and fluore

184 Horseradish peroxidase (HRP), myoglobin (Mb), and Campyl

185 most peroxidases, including the prototypical horseradish peroxidase (HRP), reportedly only oxidize io

186 the biosensor was further enhanced by using horseradish peroxidase (HRP)-Au-NP dual labels which ens

187 ign is also effective for a model analyte of horseradish peroxidase (HRP)-avidin in the dynamic range

188 be hybrids was achieved through binding of a horseradish peroxidase (HRP)-conjugated anti-fluorescein

189 etramethyl benzidine (TMB) after addition of horseradish peroxidase (HRP)-conjugated anti-IgG antibod

190 immobilized between the primary antibody and horseradish peroxidase (HRP)-conjugated secondary antibo

191 -positive endosomes after internalization of horseradish peroxidase (HRP)-containing conjugates inhib

192 -sensitive hydrogen peroxide sensor by using horseradish peroxidase (HRP)-immobilized conducting poly

193 Then the widely used horseradish peroxidase (HRP)-labeled antibody (anti-CEA)

194 their respective Ab spots was detected using horseradish peroxidase (HRP)-labeled anticytokine Abs an

195 , and a direct competitive immunoassay using horseradish peroxidase (HRP)-labeled tracers was perform

196 Horseradish peroxidase (HRP)-labelled cortisol is added

197 MLPA products and following hybridization, a horseradish peroxidase (HRP)-labelled DNA secondary prob

198 cally or electrochemically monitored using a horseradish peroxidase (HRP)-labelled DNA secondary prob

199 red single-stranded DNA (ssDNA) includes the horseradish peroxidase (HRP)-like DNAzyme, optimum-lengt

200 The initial rates of horseradish peroxidase (HRP)-mediated enzymatic reaction

201 ed detection platform is described using the horseradish peroxidase (HRP)-mimicking DNAzyme as an amp

202 implemented to yield the hemin/G-quadruplex horseradish peroxidase (HRP)-mimicking DNAzyme as cataly

203 Using the horseradish peroxidase (HRP)-O-phenylenediamine-H2O2 ele

204 gold nanoparticles (AuNPs) bearing adsorbed horseradish peroxidase (HRP).

205 nsaminase (ALT), pyruvate oxidase (POx), and horseradish peroxidase (HRP).

206 reaction involving lactate oxidase (LOX) and horseradish peroxidase (HRP).

207 tem, and the method is also demonstrated for horseradish peroxidase (HRP).

208 lated SWNTs through enzymatic catalysis with horseradish peroxidase (HRP).

209 ce (TER) and the transmonolayer diffusion of horseradish peroxidase (HRP).

210 yoglobin (HHMb), dehaloperoxidase (DHP), and horseradish peroxidase (HRP).

211 idized by H2O2 in the presence of the enzyme horseradish peroxidase (HRP).

212 cose oxidase (GO) from Aspergillus niger and horseradish peroxidase (HRP).

213 ditional oligonucleotide-conjugated Ramp and horseradish peroxidase (HRP).

214 m dots, green fluorescent proteins (GFPs) or horseradish peroxidase (HRP).

215 up using a secondary antibody conjugated to horseradish peroxidase (HRP).

216 oduce thiocholine, which is then oxidized by horseradish peroxidase (HRP).

217 Direct electrochemistry of horseradish peroxidase (HRP)/nano-SnO(2) composite has b

218 ts from traditional immunoassays, which used horseradish peroxidase (HRP, R(2) = 0.964) and fluoresce

219 Ps-PAMAM interface and anti-PSA labeled with horseradish peroxidase (HRP-labeled anti-PSA) as seconda

220 rier integrity was determined by quantifying horseradish peroxidase (HRP; 44 kDa) flux across cells g

221 the sandwich is completed by conjugation of horseradish-peroxidase (HRP)-labeled anti-rabbit IgG.

222 tecting glycoproteins of interest (presently horseradish peroxidase, HRP, a mannose glycoprotein) as

223 substrate and mediator for enzymatic tracer (Horseradish peroxidase--HRP).

224 oscopy by utilizing conjugates of avidin and horseradish peroxidase in a microtiter plate assay.

225 ons, we injected CTB-Au in a pale stripe and horseradish peroxidase in an adjacent thin stripe.

226 +) (a) and PPh(4)(+) (b) function similar to horseradish peroxidase in the mediated electron transfer

227 ened brains following multiple injections of horseradish peroxidase in the opposite hemisphere.

228 we retrogradely labeled these neurons using horseradish peroxidase injections into the cochlea.

229 Injection of IB4-conjugated horseradish peroxidase into a lumbar DRG resulted in int

230 means of injections of wheat germ agglutinin-horseradish peroxidase into the appropriate LGN layers.

231 abeled spinal motoneurons after injection of horseradish peroxidase into the tibialis anterior (TA) m

232 Permeability was assessed by encapsulating horseradish peroxidase into vesicles and measuring the a

233 The enzyme horseradish peroxidase is routinely used in immunohistoc

234 Horseradish peroxidase is utilized to generate electroch

235 lated detection antibody, (iii) streptavidin horseradish peroxidase, (iv) a wash buffer, (v) a colori

236 strong intrinsic signal amplification of IB4-horseradish peroxidase, labeled as many as 52% of unmyel

237 onfiguration involving selective capture and horseradish peroxidase-labeled detector antibodies was i

238 xtracellular structures and the range of the horseradish peroxidase-labeled guide molecule.

239 in extract was employed as an antigen, and a horseradish peroxidase-labeled polyclonal anti-goat anti

240 tion of N-cyclopropyl-N-methylaniline (3) by horseradish peroxidase leads exclusively to ring-opened

241 A horseradish peroxidase-linked short oligo was complement

242 ric hemin/G-quadruplex structure, exhibiting horseradish peroxidase mimicking functions.

243 ily decorated with anti-ERalpha antibody and horseradish peroxidase (MP-Ab-HRP) were used to efficien

244 Horseradish peroxidase-, myeloperoxidase-, and cyclooxyg

245 ripherally (wheat germ agglutinin-conjugated horseradish peroxidase or cholera toxin B: masseter or o

246 structures are accessible to small tracers (horseradish peroxidase or ruthenium red) applied to cell

247 as much higher for p31-49 or 33-mer than for horseradish peroxidase, p202-220, and p57-68.

248 ucose oxidase patch became the substrate for horseradish peroxidase, patterned downstream, where fluo

249 also observed when SWNTs were modified with horseradish peroxidase prior to incorporation into redox

250 abluminal vesicles containing electron-dense horseradish peroxidase-reaction product were noted in th

251 was accompanied by accumulation of a stable horseradish peroxidase-reactive oxidant, presumably H2O2

252 In contrast to lactoperoxidase, horseradish peroxidase remains high-spin over the temper

253 phenoxazine (Amplex(R) Red) with and without horseradish peroxidase, respectively.

254 lized carbon nanospheres (CNSs) labeled with horseradish peroxidase-secondary antibodies (HRP-Ab2).

255 Free base and Pd porphyrin derivatives of horseradish peroxidase show long-lived excited states th

256 Here we report a split horseradish peroxidase (sHRP) as a sensitive and specifi

257 ith the sulfenic acid-specific probe DAz and horseradish peroxidase-streptavidin Western blotting dem

258 dish peroxidase conjugate and a precipitable horseradish peroxidase substrate.

259 With the horseradish peroxidase system and [(35)S]GSH, GRx enhanc

260 ly show that CNT material is oxidized in the horseradish peroxidase system but with half-lives of abo

261 rd to the biotransformability of CNTs in the horseradish peroxidase system we incubated: (a) (14)C-la

262 sterol oxidase coupled with the luminol-H2O2-horseradish peroxidase system.

263 of the well plate and first screened using a horseradish-peroxidase-tagged (HRP) mouse antibody to qu

264 ecipitation reaction catalyzed by the enzyme horseradish peroxidase that is conjugated to the antibod

265 AFM1 antibody and the conjugate of AFB1 with horseradish peroxidase the conditions of the chemilumine

266 When compared with Au NPs and horseradish peroxidase, the Au/Ag NPs provide 150- and 1

267 peroxidase activity in solution compared to horseradish peroxidase, the ten heme cofactors enable ex

268 tial controlled ligation of the redox enzyme horseradish peroxidase to a macroscopic planar electrode

269 es isthmotectal axon branching, we have used horseradish peroxidase to examine axons of Xenopus after

270 ndary detection antibody was conjugated with horseradish peroxidase to provide a signal enhancement b

271 ermining the extravasation of Evans Blue and horseradish peroxidase tracers, respectively.

272 Amperometric horseradish peroxidase transduction of hydrogen peroxide

273 efficiently catalyzed by nanomolar levels of horseradish peroxidase under peroxide-free conditions.

274 in spontaneous vesicle endocytosis judged by horseradish peroxidase uptake after cholesterol depletio

275 ake, fluorescein isothiocyanate-dextran, and horseradish peroxidase uptake, indicating that CIP4 affe

276 Horseradish peroxidase uses the hydrogen peroxide to pro

277 our study on the conformational dynamics of horseradish peroxidase using single-molecule multiparame

278 ed in competitive binding experiments with a horseradish peroxidase-vancomycin conjugate.

279 and then, after various recovery times (R), horseradish peroxidase was applied to the spinal cord at

280 In a parallel study, horseradish peroxidase was injected into the mammillary

281 Cholera toxin subunit B conjugated to horseradish peroxidase was then injected into the thumb

282 Commercially available Pin1 conjugated to horseradish peroxidase was used for chemiluminescent det

283 For two unrelated model antigens (RNase and horseradish peroxidase), we found that only the less dig

284 Using activity-dependent markers FM1-43 and horseradish peroxidase, we found that MII inactivation g

285 tions of wheat germ agglutinin conjugated to horseradish peroxidase were placed in the forepaw region

286 nked glucose oxidase and streptavidin-linked horseradish peroxidase were sequentially patterned in se

287 different enzymes (alkaline phosphatase and horseradish peroxidase) were used in one immunoassay and

288 zymatic system, based on glucose oxidase and horseradish peroxidase, were immobilized on a biocompati

289 luorescent tracers and wheat germ agglutinin-horseradish peroxidase (WGA-HRP) in dorsal (PMD) and ven

290 ntravitreal wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP) injections revealed dif

291 jections of wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP) into the muscle.

292 tracer wheat germ agglutinin conjugated with horseradish peroxidase (WGA-HRP) were made into dorsal/v

293 ), and wheat germ agglutinin conjugated with horseradish peroxidase (WGA-HRP) were placed in topograp

294 netic parameters Km and kcat are better than horseradish peroxidase which makes it a superior enzyme.

295 n was done based on the anti rabbit IgG HRP (Horseradish Peroxidase) which binds to the immune comple

296 from enzymatic reaction of uricase and HRP (horseradish peroxidase), which is involved in oxidizing

297 peroxide will be further reduced to water by horseradish peroxidase, which results in an amperometric

298 r was simplified by replacing the amplifying horseradish peroxidase with bilirubin oxidase (BOD).

299 17) mol mm(-2) obtained for the enzyme label horseradish peroxidase with chemiluminescence detection)

300 a bienzymatic sensor phase (glucose oxidase/horseradish peroxidase) with ferrocyanide as electron-tr