ライフサイエンスコーパス: peroxidase

1 atic system (glucose oxidase and horseradish peroxidase).

2 Con A, and the biotin-binding protein avidin-peroxidase.

3 recedent for the formation of Fe(IV)-OH in a peroxidase.

4 ptor subtypes 3, 4, and 5 as well as thyroid peroxidase.

5 itu conversion of a precatalyst to an active peroxidase.

6 zymes are unique Cys-based, lipoyl-dependent peroxidases.

7 d heme peroxidase with homology to mammalian peroxidases.

8 nto the role of the Asp-His-Fe triad of heme peroxidases.

9 s large amount of uric acid and inflammatory peroxidases.

10 oxidation of uric acid by inflammatory heme peroxidases.

11 In animal models, glutathione peroxidase 1 (GPx1) activity is reduced after acute nois

12 Human glutathione peroxidase 1 could thereby also be produced, and we coul

13 jor antioxidant defense enzymes, glutathione peroxidase 1 knockout mice are protected during lethal p

14 C57Bl6 and glutathione peroxidase 1 knockout mice.

15 peroxide in bacterially infected glutathione peroxidase 1 macrophages and that restoring hydrogen per

16 Infected glutathione peroxidase 1 mice showed an early and significant, albei

17 ffect was suppressed by treating glutathione peroxidase 1 mice with an interleukin-1 receptor antagon

18 Arabidopsis mutants deficient in Ascorbate Peroxidase 1 showed attenuated hydrotropic root bending.

19 xpression and protein abundance of versatile peroxidase 1, which directly degrades lignin.

20 ase-2, hormone sensitive lipase, glutathione peroxidase-1, and myosin heavy chain IIa in quadriceps o

21 ants, superoxide dismutase 1 and glutathione peroxidase-1, were significantly upregulated compared wi

22 We recently reported enhanced ascorbate peroxidase 2 (APEX2) as a broadly applicable genetic tag

23 We report a glutathione peroxidase 3 (AaGPx3) involved in the complex signalling

24 1), von Willebrand factor (VWF), glutathione peroxidase 3 (GPX3), and platelet-derived growth factor

25 Glutathione peroxidase 4 (GPX4) and arachidonic acid 15-lipoxygenase

26 The antioxidant enzyme glutathione peroxidase 4 (Gpx4) is a key regulator of oxidative stre

27 The selenoenzyme glutathione peroxidase 4 (Gpx4) is a major scavenger of phospholipid

28 Small molecules that inhibit glutathione peroxidase 4 (GPX4), a phospholipid peroxidase, cause le

29 death triggered by inhibition of glutathione peroxidase 4 (GPX4), which catalyzes the reduction of li

30 that is critically dependent on glutathione peroxidase 4 (GPX4).

31 the phospholipid hydroperoxidase glutathione peroxidase 4 (GPX4).

32 egulating the antioxidant enzyme glutathione peroxidase-4.

33 inc superoxide dismutaseP< 0.05; glutathione peroxidase 4P< 0.01] and increased lipoxygenase expressi

34 Here, we demonstrate that peroxidase A from D. discoideum (DdPoxA) is a stable, mo

35 ide repressed lignin formation, in line with peroxidases activating monolignols for lignin polymeriza

36 The actual peroxidase activation step corresponds to subsequent sid

37 gand, thereby increasing the population of a peroxidase active state, which is a key non-native confo

38 al ligation site, and it represents the true peroxidase-active structure of cyt c.

39 (DeltaMakatG1) showed decreased catalase and peroxidase activities and significantly increased suscep

40 peroxide dismutase, catalase and glutathione peroxidase activities in H2O2 treated CCD and Caco-2 cel

41 ontrary to the expectation that catalase and peroxidase activities should be mutually antagonistic, p

42 otein with phospholipase A2 (aiPLA2) and GSH peroxidase activities, protects lungs from oxidative str

43 sion between oxidation states is mediated by peroxidase activity (oxidation) and l-cysteine (reductio

44 rature range (4-70 degrees C) and shows high peroxidase activity from 2 to 6pH.

45 esis of OVA-specific IgE and skin eosinophil peroxidase activity in mice with ongoing skin allergy.

46 Although MtrC showed lower peroxidase activity in solution compared to horseradish

47 Moreover, eosinophil peroxidase activity in the skin and production of IL-4,

48 ide the matrix, without interfering with its peroxidase activity in vitro Remarkably, the processing

49 on; however, treatment to reduce glutathione peroxidase activity increased 5-LO metabolite production

50 This peroxidase activity is caused by a conformational change

51 ifications as an essential component for the peroxidase activity of "native" cyt c.

52 experiments we investigate the structure and peroxidase activity of cyt-c in its membrane-bound state

53 ates cytochrome c reduction and inhibits the peroxidase activity of cytochrome c, which is involved i

54 The peroxidase activity of nanozyme is selectively quenched

55 ), and GSH plus Grx1 was able to support the peroxidase activity of Prx2.

56 Due to the excellent peroxidase activity of Pt-Au NPs, they emit strong visib

57 From a biochemical point of view the peroxidase activity of the Abeta-heme complex seemed qui

58 SIRT2 binds, deacetylates, and inhibits the peroxidase activity of the antioxidant protein peroxired

59 x with heme exhibited a significantly higher peroxidase activity than Abeta(40)-heme.

60 s based on Pt-Au bimetal NPs possessing high peroxidase activity toward 3,3',5,5'-tetramethylbenzidin

61 Second, peroxidase activity was observed in heme-containing mice

62 Cytochrome c can acquire peroxidase activity when it binds to cardiolipin in mito

63 The heme is poised for peroxidase activity with water bound in place of Met80,

64 s dimeric structure, but diminished Asp f3's peroxidase activity, and extended the alpha-helix with t

65 ) and found that in addition to the expected peroxidase activity, AnPrx6 can act as a molecular chape

66 conditions, however, cyt c gains cardiolipin peroxidase activity, translocates into the cytosol to en

67 yase activity and significantly increases of peroxidase Activity.

68 W233F) completely abolishes the Cc-dependent peroxidase activity.

69 trads in the context of both GTP-binding and peroxidase activity.

70 act as a relay in radical abstraction during peroxidase activity.

71 m catalytic hemin/G-quadruplex DNAzymes with peroxidase activity.

72 are shown to possess significantly enhanced peroxidase activity.

73 terintuitive that native cyt c would exhibit peroxidase activity.

74 g both ascorbate (Asc) and cytochrome c (Cc) peroxidase activity.

75 Ectopic expression of a membrane-bound peroxidase allowed us to map synaptic sites along PN den

76 s the fluid-phase endocytosis of horseradish peroxidase and also specifically induced the transport o

77 ivity was observed with a 4-fold increase in peroxidase and approximately 3-fold increases in catalas

78 ar models support a critical role for a heme peroxidase and enzymatic sources of reactive oxygen spec

79 s were retrogradely labeled with horseradish peroxidase and examined in retinal wholemounts.

80 etected GFP with pre-embedding avidin-biotin-peroxidase and GABA with post-embedding immunogold label

81 Additionally, the activities of peroxidase and glutathione peroxidase, and the peroxired

82 activities of hepatic catalase, glutathione peroxidase and glutathione S transferase compared with t

83 fficient electronic coupling between tobacco peroxidase and graphite and to the formation of intra- a

84 on of a cadre of cytosolic (e.g. glutathione peroxidase and heat shock proteins) and mitochondrial ad

85 the polymer solutions containing horseradish peroxidase and hydrogen peroxide.

86 of positive selection for genes involved in peroxidase and hypoxia to enable its highland adaptation

87 tants also exhibited decreased extracellular peroxidase and laccase activities and showed defects in

88 sites, and these cleavages disrupt both the peroxidase and phospholipase A2 activities of Prdx6.

89 nzyme cocktail (glucose oxidase, horseradish peroxidase and potassium ferrocyanide as mediator of the

90 respiratory complexes, enhances hemeprotein peroxidase and reactive oxygen species scavenging activi

91 s glutathione reductase, catalase, ascorbate peroxidase and superoxide dismutase together with xantho

92 The activities of catalase, glutathione peroxidase and superoxide dismutase were significantly l

93 s are exceptional functional replicas of the peroxidases and cytochrome P450 oxidizing enzymes.

94 yphenols) and enzymes (ascorbic peroxidases, peroxidases and polyphenol oxidases) involved in the ant

95 of cytosolic and mitochondrial tryparedoxin peroxidases and their substrate (tryparedoxin) and iron

96 ies of antioxidant (superoxide dismutase and peroxidase) and defense enzymes (polyphenol oxidase and

97 nels on these devices using glucose oxidase, peroxidase, and 2,2'-azino-bis(3-ethylbenzothiazoline-6-

98 sed levels of autoantibodies against thyroid peroxidase, and also exhibited the strongest disease imp

99 tic assay using glucose oxidase, horseradish peroxidase, and ferrocyanide as electron-transfer mediat

100 uropeptides, major basic protein, eosinophil peroxidase, and many US Food and Drug Administration-app

101 the activities of peroxidase and glutathione peroxidase, and the peroxiredoxin abundance were increas

102 ior performance in Western blotting, in both peroxidase- and fluorophore-linked form.

103 roid-stimulating hormone levels, and thyroid peroxidase antibodies.

104 d with a fluorophore-labeled polyclonal anti-peroxidase antibody (anti-HRP-Alexa Fluor 488).

105 mone (TSH), free thyroxine (FT4) and thyroid peroxidase antibody (TPOAb) positivity.

106 yroid-stimulating hormone (TSH), and thyroid peroxidase antibody (TPOAb) were obtained from medical r

107 Here, we applied engineered ascorbate peroxidase (APEX) to map the proteome at EMCs in live HE

108 Here, we used enhanced ascorbate peroxidase (APEX)-tagged PB2 proteins and electron micro

109 abeling mediated by engineered ascorbic acid peroxidase (APEX).

110 An engineered peroxidase, APEX2, is genetically targeted to a cellular

111 ated with lower catalase (CAT) and ascorbate peroxidase (APX) activities, leading to fruits with lowe

112 uperoxide dismutase (CuZn-SOD) and ascorbate peroxidase (APX) constitute first line of defence agains

113 y aimed to investigate the role of ascorbate peroxidase (APX), guaiacol peroxidase (GPX), polysacchar

114 ne (NMH) ligand into an engineered ascorbate peroxidase (APX2) overcomes the reliance on the conserve

115 hysiological studies suggest that homologous peroxidases are already present in mycetozoan eukaryotes

116 Secreted peroxidases are well-known components of damage-induced

117 rried out by glucose oxidase and horseradish peroxidase as a model system, here we study the kinetics

118 am genes, including those encoding ascorbate peroxidase (AtApx2) and heat shock proteins [AtHsp18.1-C

119 scence, Alexa-fluorophores, and horse radish peroxidase-based bead assays, enabling multiplexed detec

120 never restricted to them and their class II peroxidases, because lignin modification is known to occ

121 d electrocatalytic properties of the present peroxidase biosensor that operates in the 0.3 V </= E </

122 and L mice in liver (except for Glutathione Peroxidase), brain or mammary glands.

123 arkers, as well as the release of eosinophil peroxidase by eosinophils in the bronchial mucosa, was m

124 able to cause an increase in the enzymatic (peroxidase, catalase and phenylalanine ammonium lyase (P

125 Here, we show that peroxidase-catalyzed proximity labeling can be combined

126 al analysis indicated that EGCG prevents the peroxidase-catalyzed reaction by reverting the reactive

127 ch a method, termed APEX-RIP, which combines peroxidase-catalyzed, spatially restricted in situ prote

128 tathione peroxidase 4 (GPX4), a phospholipid peroxidase, cause lethal accumulation of lipid peroxides

129 -diaminobenzidine by endocytosed horseradish peroxidase, causing an increase in the vesicle density,

130 the 1.5-A crystal structure of cytochrome c peroxidase (CCP) compound I (CmpI) using data obtained w

131 class I heme peroxidases [TcAPx-cytochrome c peroxidase (CcP)], suggesting both ascorbate (Asc) and c

132 Microbial cytochrome c peroxidases (Ccp) have been studied for 75 years, but th

133 (FI) platform was developed with horseradish peroxidase chemiluminescence as the reporter system, the

134 Class III peroxidases (CIIIPRX) catalyze the oxidation of monolign

135 ells are incubated with a hapten-horseradish peroxidase conjugate (hapten-HRP), which is subsequently

136 introduction of the streptavidin-horseradish peroxidase conjugate that catalytically converted the 3,

137 th the electrochemical reporter streptavidin-peroxidase conjugate.

138 After rinsing, peroxidase-conjugated anti-IgG is drawn through the memb

139 les, which then allow binding of horseradish-peroxidase-conjugated avidin (avidin-HRP).

140 abeling cleared tissues based on horseradish peroxidase conversion of diaminobenzidine to a colored i

141 alveolar lavage eosinophilia, and eosinophil peroxidase deposition in bronchial mucosa.

142 , whereas airway eosinophilia and eosinophil peroxidase deposition were blunted but not eliminated.

143 We used viral vectors to deliver peroxidase derivatives, which catalyze production of an

144 d DNA probes, followed by an antidigoxigenin-peroxidase detection system at screen-printed carbon ele

145 in-like domains and the catalytically active peroxidase domain.

146 ities of TAML activators and the horseradish peroxidase enzyme are critically compared.

147 based upon small- molecule, full-functional peroxidase enzyme replicas called "TAML activators".

148 was analyzed using a simplified horseradish peroxidase enzyme-based colorimetric scheme by simple vi

149 e is made of alcohol oxidase and horseradish peroxidase enzymes immobilized on to a carbon nanotube m

150 ntrast, activities of polyphenol oxidase and peroxidase enzymes were substantially lower in fruit kep

151 own by human myeloperoxidase and horseradish peroxidase enzymes, revealing that incidental biological

152 Here we show eosinophil peroxidase (EPO), an abundant granule protein released b

153 resence of autoantibodies against eosinophil peroxidase (EPX) and anti-nuclear antibodies was investi

154 are nasal, pharyngeal, and sputum eosinophil peroxidase (EPX) levels with induced sputum eosinophil p

155 tion and were also deficient in eosinophilic peroxidase (EPX).

156 eome, as well as multiple lysyl oxidases and peroxidases, establish homology with silk-associated mat

157 esponses, with a high induction of ascorbate peroxidase expression.

158 Live-cell proximity labeling using APEX peroxidase followed by anti-biotin enrichment and mass s

159 estigated whether DypB, the lignin-degrading peroxidase from Rodococcus jostii, depolymerizes lignin

160 This peroxidase function plays a key role during apoptosis.

161 Two mitochondrial-localized rice ascorbate peroxidase genes fused to DsRed and successfully co-loca

162 wed that exposure to LS upregulated type III peroxidase genes, of which some are involved in lignin b

163 s surrounding LRP where it controls a set of peroxidase genes, which maintain reactive oxygen species

164 ); most likely through enhancing glutathione peroxidase (GPx) activity in liver (4.3-fold of control)

165 sed superoxide levels, decreased glutathione peroxidase (GPx) activity, decreased glutathione levels,

166 as it plays an important role in glutathione peroxidase (GPx) activity.

167 The antioxidant glutathione peroxidase (GPx) and inflammation biomarkers, including

168 (NO), superoxide dismutase, and glutathione peroxidase (GPX) levels in serum were measured with enzy

169 clamide decreased GSH levels and glutathione peroxidase (GPx) of PMNs after exposed to live B. pseudo

170 role of ascorbate peroxidase (APX), guaiacol peroxidase (GPX), polysaccharides, and protein contents

171 of the antioxidant selenoenzyme glutathione peroxidase (GPx), via oxidation to the corresponding spi

172 selens 7 were poor mimics of the glutathione peroxidase (GPx)-enzymes, nitroebselens 3, 6, and 11b an

173 G418, whereas expression of the glutathione peroxidases GPX1 and GPX2 was marginally affected.

174 s converging on the phospholipid glutathione peroxidase (GPX4), a selenocysteine-containing enzyme th

175 ically, over-expression of stromal ascorbate peroxidase (H2O2 scavenger) or treatment with DCMU (phot

176 G solutions with and without addition of the peroxidase/H2O2 was examined.

177 -ions differed from those obtained by adding peroxidase/H2O2.

178 ility of the mixed AX/BG system treated with peroxidase/H2O2.

179 DPH oxidases as well as by secreted type III peroxidases has a great impact on cell wall properties d

180 Typical peroxidases have a five-coordinate heme with a vacant di

181 (trehalase, glucose oxidase, and horseradish peroxidase) have been coimmobilized in calcium alginate

182 catalyzed reaction by reverting the reactive peroxidase heme (compound I:oxoiron) back to its native

183 terial protein conjugated with a horseradish peroxidase homopolymer (ProtA-HRP40).

184 is link, we tagged vesicles with horseradish peroxidase (HRP) - a haem-containing plant enzyme - or a

185 In the biosensor, horseradish peroxidase (HRP) and glucose oxidase (GOD) were electrod

186 which is easily monitored using horseradish peroxidase (HRP) and o-dianisidine.

187 In the catalytic reaction, horseradish peroxidase (HRP) enzyme is used for catalyzing the non-f

188 Horse radish peroxidase (HRP) is one of the most common enzymes used

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

190 m albumin, primary antibody and Horse Radish Peroxidase (HRP) tagged secondary antibody on the surfac

191 antibody, itself conjugated with horseradish peroxidase (HRP) to produce a measurable signal.

192 resin (SU-8) on the stability of horseradish peroxidase (HRP) was studied in both a short-term experi

193 el protein streptavidin bound to horseradish peroxidase (HRP) was successfully immobilized onto the s

194 racellular oxidoreductase enzyme horseradish peroxidase (HRP) were evaluated to maximize incorporatio

195 oupled a model cargo (the enzyme horseradish peroxidase (HRP)) to anti-ICAM and separated a 1:2 antib

196 effective for a model analyte of horseradish peroxidase (HRP)-avidin in the dynamic range of 0.1-3.0

197 enzidine (TMB) after addition of horseradish peroxidase (HRP)-conjugated anti-IgG antibodies.

198 between the primary antibody and horseradish peroxidase (HRP)-conjugated secondary antibody onto AgNP

199 Horseradish peroxidase (HRP)-labelled cortisol is added to compete w

200 s and following hybridization, a horseradish peroxidase (HRP)-labelled DNA secondary probe complement

201 LT), pyruvate oxidase (POx), and horseradish peroxidase (HRP).

202 oproteins of interest (presently horseradish peroxidase, HRP, a mannose glycoprotein) as the biochemi

203 d mediator for enzymatic tracer (Horseradish peroxidase--HRP).

204 huttle, ferri-cytochrome c (cyt c) acts as a peroxidase; i.e., it catalyzes the oxidation of organic

205 hat accumulation and in situ activation of a peroxidase improves biomass digestibility.

206 using isoeugenol polymerised by horse radish peroxidase in aqueous solution.

207 ility and inactivation kinetics of blueberry peroxidase in model systems (McIlvaine buffer, pH=3.6, t

208 compared with evolutionary-related mammalian peroxidases in the context of non-specific immune defens

209 We have named this protein "staphylococcal peroxidase inhibitor" (SPIN).

210 tion analogous to the substrate in ascorbate peroxidase is essential for both decarboxylations, while

211 The Trypanosoma cruzi ascorbate peroxidase is, by sequence analysis, a hybrid type A mem

212 ion antibody, (iii) streptavidin horseradish peroxidase, (iv) a wash buffer, (v) a colorimetric subst

213 ansferase 2 and 3, glutathione S-transferase peroxidase kappa 1, and glutathione peroxidase) than the

214 isoniazid must be activated by the catalase-peroxidase KatG.

215 involving selective capture and horseradish peroxidase-labeled detector antibodies was implemented o

216 d using biotin-anti-TGF and conjugation with peroxidase-labeled streptavidin (poly-HRP-Strept) polyme

217 as supports for antibody immobilisation and peroxidase-labelled AZA as a tracer is detailed.

218 The as-prepared nanocomposites exhibit high peroxidase-like activity for the catalytic conversion of

219 is study, we have investigated the intrinsic peroxidase-like activity of citrate-capped AuNPs (perAux

220 The peroxidase-like activity of CoOxH-GO is utilized herein

221 1 C-terminal moiety, which also inhibits the peroxidase-like activity of heme, and (ii) MF6p/HDMs fro

222 for the detection of dimethoate based on the peroxidase-like activity of silver-nanoparticles-modifie

223 tides in complex with heme revealed that the peroxidase-like activity significantly depends on the pe

224 polymers were grown on Fe3O4 nanozymes with peroxidase-like activity to create substrate binding poc

225 uses heme-containing bacterial enzymes with peroxidase-like activity to facilitate phosphotyrosine (

226 The peroxidase-like catalytic activity of the SiO2/Imi/Pt ma

227 odified graphene oxide (CoOxH-GO) possessing peroxidase-like catalytic activity, and its application

228 synthesis of supported Pt nanoparticles with peroxidase-like catalytic activity.

229 (superoxide dismutase, catalase, glutathione peroxidase, lipidic and protein peroxidation).

230 we demonstrate that a bifunctional catalase-peroxidase, MakatG1, in the locust-specific fungal patho

231 that IMiDs work primarily via inhibition of peroxidase-mediated intracellular H2O2 decomposition in

232 Using peroxidase-mediated proximity biotinylation, we captured

233 the synergy of Fenton reaction and manganese peroxidase might play an important role in DR5B dye degr

234 oximately 3% bromine content has shown novel peroxidase mimetic activity toward 3,3',5,5'-tetramethyl

235 Palladium-gold nanozyme shows excellent peroxidase mimetic activity with O-phenylenediamine in t

236 In this reaction, hemin-binding peroxidase-mimicking DNAzymes ("peroxidymes") mediate th

237 functional cupric oxide nanorods (CuONRs) as peroxidase mimics are proposed for the development of a

238 pplied for imprinting on gold nanoparticles (peroxidase mimics) and nanoceria (oxidase mimics).

239 d with anti-ERalpha antibody and horseradish peroxidase (MP-Ab-HRP) were used to efficiently capture

240 s (TCM), which were transgenic for a myeloid peroxidase (MPO)-specific TCR.

241 Analysis of a thylakoidal ascorbate peroxidase mutant (tapx), the (1)O2-retrograde signaling

242 le peroxidase (VP) is a high redox-potential peroxidase of biotechnological interest that is able to

243 structure (2.5 A resolution) of a mycetozoan peroxidase of this superfamily shows the presence of a p

244 ents of anti-Dig and anti-FITC conjugated to peroxidase or alkaline phosphatase, respectively.

245 Cytosolic ascorbate peroxidase over-expression has little effect on nuclear

246 The reaction of peroxides with peroxidases oxidizes the heme iron from Fe(III) to Fe(IV

247 cell death induced by inhibition of a lipid peroxidase pathway as a feature of therapy-resistant can

248 nd show that it depends on a druggable lipid-peroxidase pathway that protects against ferroptosis, a

249 rols, and polyphenols) and enzymes (ascorbic peroxidases, peroxidases and polyphenol oxidases) involv

250 peroxide dismutase (SOD), catalase (CAT) and peroxidase (POD) decreased at a later time period post t

251 y of polyphenol oxidase (PPO) and polyphenol peroxidase (POD) in fresh-cut pineapple was significantl

252 Peroxidase (POD) is an enzyme that needs to be inactivat

253 Study investigates the peroxidase potential of the nanozyme on colorimetric sub

254 oactive compounds, polyphenol oxidase (PPO), peroxidase (POX), and superoxide dismutase (SOD) enzymes

255 transferrin nor knock-out of cytosolic lipid peroxidases prevented TLF-1 lysis.

256 A new study makes use of the ascorbate peroxidase proximity-labeling proteomics approach to scr

257 the anti-p53 molecule fortilin augments the peroxidase PRX1 by protecting it against degradation and

258 functions have been attributed to class III peroxidases (PRXs) in plants, but the in planta role of

259 ansfer of a single proton is critical in the peroxidase rate-limiting step, which is very likely the

260 Cyt c-catalyzed peroxidase reactions show an initial lag phase that is c

261 uadruplex that can both bind GTP and promote peroxidase reactions.

262 Expression of peroxidase reporters in Caenorhabditis elegans shows tha

263 ar-targeted, genetically encoded hemoprotein peroxidase reporters, that both extracellular and endoge

264 ch and even surpass those of certain natural peroxidases, retains its activity at elevated temperatur

265 Here we report a split horseradish peroxidase (sHRP) as a sensitive and specific tool for t

266 tic architecture with positivity for thyroid-peroxidase-specific antibody, driven generally by varian

267 Upon hybridization, a streptavidin-peroxidase (Strep-HRP) conjugate was employed as an elec

268 the H2O2-mediated oxidation of a chromogenic peroxidase substrate (TMB), allowing the colorimetric de

269 nic leaves showed higher activity on classic peroxidase substrates than the control.

270 participate in an alternative four-component peroxidase system, HOAS/dihydrolipoyl acetyl transferase

271 plate and first screened using a horseradish-peroxidase-tagged (HRP) mouse antibody to quantify bindi

272 ysis, a hybrid type A member of class I heme peroxidases [TcAPx-cytochrome c peroxidase (CcP)], sugge

273 nsferase peroxidase kappa 1, and glutathione peroxidase) than the BN rat, suggesting that the LEW rat

274 ndria, cyt-c gains a new function as a lipid peroxidase that catalyzes the reactive oxygen species-me

275 peroxidasin 1 is a homotrimeric multidomain peroxidase that is secreted to the extracellular matrix.

276 arrier in oxidative phosphorylation and as a peroxidase that reacts with cardiolipin (CL) during apop

277 which is a selenocysteine-based glutathione peroxidase, the first found in insects.

278 activity in solution compared to horseradish peroxidase, the ten heme cofactors enable excellent elec

279 ferryl intermediate in Compound II of a heme peroxidase; the structure allows the protonation states

280 ion antibody was conjugated with horseradish peroxidase to provide a signal enhancement by the biocat

281 Oxidation of halides and thiocyanate by heme peroxidases to antimicrobial oxidants is an important co

282 Activity of polyphenol oxidase and peroxidase, total and individual phenolic content as wel

283 Levels of IgG against thyroid peroxidase (TPO) are more often elevated in CSU than tho

284 demonstrated that CYP121 performs a standard peroxidase type of reaction by observing substrate-based

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

286 n the conformational dynamics of horseradish peroxidase using single-molecule multiparameter photon t

287 Versatile peroxidase (VP) is a high redox-potential peroxidase of

288 fied cysteine residue on cytosolic ascorbate peroxidase was demonstrated using liquid chromatography-

289 proteins major basic protein and eosinophil peroxidase were more frequently detected in the bronchoa

290 autoantibodies to thyroglobulin and thyroid peroxidase were unaffected.

291 deficient for peroxiredoxins and glutathione peroxidases were equally sensitive to fatty acid hydrope

292 em, based on glucose oxidase and horseradish peroxidase, were immobilized on a biocompatible polysacc

293 show that wheat germ agglutinin horse radish peroxidase (WGA-HRP) chemically conjugated to gold nanop

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

295 ased on the anti rabbit IgG HRP (Horseradish Peroxidase) which binds to the immune complex and the re

296 tial enzymatic reaction (glucose oxidase and peroxidase), which generated a chemiluminescent signal i

297 l be further reduced to water by horseradish peroxidase, which results in an amperometric signal via

298 S-nitrosylation of peroxiredoxin-2 (Prx2), a peroxidase widely expressed in mammalian neurons, inhibi

299 , monomeric, glycosylated, and secreted heme peroxidase with homology to mammalian peroxidases.

300 ic sensor phase (glucose oxidase/horseradish peroxidase) with ferrocyanide as electron-transfer media