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

4 Our results show that horseradish and watercress genomes originated from a com

5 = 64), structurally mirroring the tetraploid horseradish and watercress genomes, originated via autop

6 es might suggest an autotetraploid origin of horseradish and watercress genomes.

7 These comparative cytogenomic maps in horseradish and watercress represent a first stepping st

8 e extent of chromosomal collinearity between horseradish and watercress, and to reconstruct the origi

9 Horseradish (Armoracia rusticana) and watercress (Nastur

10 Horseradish (Armoracia rusticana) is a plant well known

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

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

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

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

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

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

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

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

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

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

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

22 Horseradish peroxidase (HRP) and hydrogen peroxide conce

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

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

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

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

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

28 Horseradish peroxidase (HRP) as a model enzyme was co-as

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

51 s evidenced using streptavidin-conjugated to horseradish peroxidase (HRP) in the presence of luminol

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

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

54 The inhibition of horseradish peroxidase (HRP) is uncompetitive for the su

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

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

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

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

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

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

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

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

63 commercial bioreagents loaded with multiple horseradish peroxidase (HRP) molecules, recognizing the

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

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

66 The cleavage cascade also released horseradish peroxidase (HRP) pre-attached to the amplifi

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

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

69 ecific CD63 aptamer, which was conjugated to horseradish peroxidase (HRP) through biotin-streptavidin

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

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

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

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

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

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

76 Horseradish peroxidase (HRP) was conjugated to colloidal

77 Horseradish peroxidase (HRP) was encapsulated by the PNT

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

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

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

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

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

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

84 ation and can support the catalytic cycle of horseradish peroxidase (HRP) without the need of H(2)O(2

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

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

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

88 idin coated silver nanoparticles (AgNPs) and horseradish peroxidase (HRP), altogether, formed the sig

89 Here, we used receptor mutagenesis, horseradish peroxidase (HRP), and ascorbate peroxidase 2

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

91 ble high loadings of various proteins (e.g., horseradish peroxidase (HRP), bovine hemoglobin, immunog

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

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

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

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

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

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

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

99 binding of a ternary complex of T(30)-biotin/horseradish peroxidase (HRP)-biotin/streptavidin to the

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

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

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

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

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

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

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

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

108 Horseradish peroxidase (HRP)-labelled cortisol is added

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

128 hich was almost at the same level as natural horseradish peroxidase (HRP).

129 sing using antibodies that were labeled with horseradish peroxidase (HRP).

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

131 distance by randomly anchoring two pairs of horseradish peroxidase (HRP)/glucose oxidase (GOx) at th

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

133 body pairs [unconjugated and conjugated with horseradish peroxidase (HRP)] onto magnetic microbeads (

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

135 iched with a secondary antibody labeled with horseradish peroxidase (HRP-DAb).

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

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

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

139 Using polymeric horseradish peroxidase (poly-HRP, 400 HRPs) labels to pr

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

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

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

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

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

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

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

147 lly, we performed validation screens against horseradish peroxidase and carbonic anhydrase IX, and we

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

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

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

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

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

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

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

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

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

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

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

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

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

161 or Fe(IV)O/Fe(III)OH) reduction potential in horseradish peroxidase and the two-electron compound I/f

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

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

164 is nanozyme to the substrate was higher than horseradish peroxidase as a natural enzyme.

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

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

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

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

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

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

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

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

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

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

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

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

177 alysed oxidation of spermine, was coupled to horseradish peroxidase conversion of Amplex(R) Red (1-(3

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

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

180 Horseradish peroxidase cross-linked in an osmium based r

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

201 The enzyme horseradish peroxidase is routinely used in immunohistoc

202 Horseradish peroxidase is utilized to generate electroch

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

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

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

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

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

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

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

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

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

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

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

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

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

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

217 mical conformality avail the templating of a horseradish peroxidase train, which boosted the parallel

218 Amperometric horseradish peroxidase transduction of hydrogen peroxide

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

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

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

222 Horseradish peroxidase uses the hydrogen peroxide to pro

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

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

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

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

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

228 are captured by secondary antibody-poly-HPR (horseradish peroxidase) bioconjugates containing 400 HRP

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

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

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

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

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

234 the mixture of enzymes (glucose oxidase and horseradish peroxidase), as well as the ferrocyanide, me

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

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

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

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

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

240 lysis of surfaces pre-modified with enzymes (horseradish peroxidase, alkaline phosphatase and glucose

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

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

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

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

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

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

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

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

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

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

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

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

253 tions catalyzed by AChE, choline oxidase and horseradish peroxidase, leading to production of hydroge

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

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

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

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

258 system uses two enzymes, alcohol oxidase and horseradish peroxidase, to correlate ethanol sweat conce

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

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

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

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

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

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

265 Horseradish peroxidase-conjugated antibody binds to the

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

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

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

269 Horseradish peroxidase-conjugated streptavidin was used

270 parallel catalytic processing in individual horseradish peroxidase-containing Ru(4)PCVs, and chemica

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

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

273 A horseradish peroxidase-linked short oligo was complement

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

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

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

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

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

279 cific enzyme models such as chymotrypsin and horseradish peroxidase.

280 biotin used in conjunction with streptavidin-horseradish peroxidase.

281 tes were filled intracellularly in vivo with horseradish peroxidase.

282 tric output upon conjugation to streptavidin-horseradish peroxidase.

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

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

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

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

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

288 viously reported for nitric oxide binding to horseradish peroxidase.

289 polymerized by biocatalysis with laccase or 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 pability comparable to those of conventional horseradish-peroxidase-conjugated secondary antibodies,

294 g for pairing nanobodies and then prepared a horseradish-peroxidase-labeled nanobody using a mild con

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

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

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

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

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