ライフサイエンスコーパス: horseradish

1 ied that have hitherto not been described in horseradish.

2 n to the horseradish functional food status, horseradish above- and underground autolysates, together

3 Wasabi, horseradish and mustard owe their pungency to isothiocya

4 occoli, white cabbage, garden cress, radish, horseradish and papaya.

5 Horseradish (Armoracia rusticana) is a plant well known

6 Detailed analyses of horseradish autolysates led to the identification of a n

7 To verify its possible contribution to the horseradish functional food status, horseradish above- a

8 ion was discovered for a scIDS from juvenile horseradish leaf beetles, Phaedon cochleariae.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

66 Horseradish peroxidase (HRP) typically oxidizes aniline

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

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

69 Horseradish peroxidase (HRP) was conjugated to colloidal

70 Horseradish peroxidase (HRP) was encapsulated by the PNT

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 Horseradish peroxidase (HRP)-labelled cortisol is added

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

147 > 200 MHz are important to stabilization of horseradish peroxidase and yeast alcohol dehydrogenase i

148 Anterograde transport of horseradish peroxidase applied to the olfactory epitheli

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

168 Horseradish peroxidase cross-linked in an osmium based r

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

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

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

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

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

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

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

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

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

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

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

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

181 Horseradish peroxidase has been demonstrated to catalyze

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

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

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

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

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

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

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

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

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

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

192 The enzyme horseradish peroxidase is routinely used in immunohistoc

193 Horseradish peroxidase is utilized to generate electroch

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

209 Amperometric horseradish peroxidase transduction of hydrogen peroxide

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

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

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

213 Horseradish peroxidase uses the hydrogen peroxide to pro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

257 Horseradish peroxidase-, myeloperoxidase-, and cyclooxyg

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

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

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

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

262 Horseradish peroxidase-conjugated antibody binds to the

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

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

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

266 Horseradish peroxidase-conjugated streptavidin was used

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

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

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

270 A horseradish peroxidase-linked short oligo was complement

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

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

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

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

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

276 tes were filled intracellularly in vivo with horseradish peroxidase.

277 tric output upon conjugation to streptavidin-horseradish peroxidase.

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

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

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

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

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

283 viously reported for nitric oxide binding to horseradish peroxidase.

284 polymerized by biocatalysis with laccase or horseradish peroxidase.

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

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

287 ed using wheat germ agglutinin conjugated to horseradish peroxidase.

288 cific enzyme models such as chymotrypsin and horseradish peroxidase.

289 biotin used in conjunction with streptavidin-horseradish peroxidase.

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

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

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

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

294 miluminescent or chromogenic detection using horseradish peroxide and alkaline phosphatase substrates

295 ionalize the upconversion nanoparticles with horseradish peroxidise (HRP) for catalytic colorimetric

296 zymes such as alkaline phosphatase (ALP) and horseradish peroxidise (HRP).

297 investigates the main aroma constituents of horseradish roots in general by analysing the aroma prof

298 et in umecyanin (UMC), the stellacyanin from horseradish roots, and the axial Met89 into a Gln in CBP

299 potential to influence the overall aroma of horseradish roots, like (3S,3aS,7aR)-wine lactone and 3-

300 nalysing the aroma profiles of six different horseradish varieties, with one variety grown in two dif