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 biotin used in conjunction with streptavidin-horseradish peroxidase.

3 tes were filled intracellularly in vivo with horseradish peroxidase.

4 tric output upon conjugation to streptavidin-horseradish peroxidase.

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

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

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

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

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

10 viously reported for nitric oxide binding to horseradish peroxidase.

11 polymerized by biocatalysis with laccase or horseradish peroxidase.

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

13 cific enzyme models such as chymotrypsin and horseradish peroxidase.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

48 Anterograde transport of horseradish peroxidase applied to the olfactory epitheli

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

69 Horseradish peroxidase-conjugated antibody binds to the

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

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

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

73 Horseradish peroxidase-conjugated streptavidin was used

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

75 pability comparable to those of conventional horseradish-peroxidase-conjugated secondary antibodies,

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

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

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

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

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

81 Horseradish peroxidase cross-linked in an osmium based r

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 Horseradish peroxidase has been demonstrated to catalyze

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

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

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

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

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

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

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

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

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

107 Horseradish peroxidase (HRP) and hydrogen peroxide conce

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 Horseradish peroxidase (HRP) was conjugated to colloidal

165 Horseradish peroxidase (HRP) was encapsulated by the PNT

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

197 Horseradish peroxidase (HRP)-labelled cortisol is added

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

238 The enzyme horseradish peroxidase is routinely used in immunohistoc

239 Horseradish peroxidase is utilized to generate electroch

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

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

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

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

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

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

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

247 A horseradish peroxidase-linked short oligo was complement

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

276 Amperometric horseradish peroxidase transduction of hydrogen peroxide

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

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

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

280 Horseradish peroxidase uses the hydrogen peroxide to pro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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