ライフサイエンスコーパス: peroxidase

1 se of 1.31% and a completely inactivation of peroxidase.

2 ge inflammatory markers IL-16 and eosinophil peroxidase.

3 itu conversion of a precatalyst to an active peroxidase.

4 nd triglyceride, while increased glutathione peroxidase.

5 of gliadin after incubation in streptavidin-peroxidase.

6 -mimicking activity and chitin-AcOH mirrored peroxidase.

7 compared with previously described ascorbate peroxidases.

8 valuable alternative to devices that rely on peroxidases.

9 ht thiols, Prxs, GPxs, and other thiol-based peroxidases.

10 s large amount of uric acid and inflammatory peroxidases.

11 d heme peroxidase with homology to mammalian peroxidases.

12 id 2 related factor 2 (Nrf2) and glutathione peroxidase 1 (Gpx1) mRNA in both male and female BXD84/R

13 de dismutase 2 (SOD2), catalase, glutathione peroxidase 1 (GPX1), and heme oxygenase 1 (Hmox1) and tr

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

15 horseradish peroxidase (HRP), and ascorbate peroxidase 2 (APEX-2) proximity labelling, alongside lig

16 Using a modified enhanced ascorbate peroxidase 2 (APEX2) approach with rapamycin-dependent t

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

18 l activity of the selenoproteins glutathione peroxidase 3 (GPx3; <86.9 ng mL(-1)) and iodothyronine d

19 The expression of glutathione peroxidase 4 (GPX4) in H295R cells, however, is signific

20 The selenium-dependent glutathione peroxidase 4 (GPX4) inhibits ferroptosis, converting uns

21 The enzyme glutathione peroxidase 4 (GPX4) is a central regulator of ferroptosi

22 Glutathione peroxidase 4 (GPX4) is essential for cell membrane repai

23 redox homeostasis maintained by glutathione peroxidase 4 (GPX4) is required for STING activation.

24 -dependent lipid hydroperoxidase glutathione peroxidase 4 (GPX4) prevents ferroptosis by converting l

25 Glutathione peroxidase 4 (GPX4) protects against lipid peroxidation

26 Glutathione peroxidase 4 (GPX4) uses glutathione to protect cells fr

27 d can be exploited by inhibiting glutathione peroxidase 4 (GPX4) with small-molecules.

28 he ferroptosis-inhibiting enzyme glutathione peroxidase 4 (GPX4)(10).

29 id hydroperoxide-reducing enzyme glutathione peroxidase 4 (GPX4)(3,4) and radical-trapping antioxidan

30 nless the lipid hydroperoxidase, glutathione peroxidase 4 (GPX4), reduces these toxic lipid species.

31 e metabolism pathways, including glutathione peroxidase 4 (GPX4), which protected cells from chemothe

32 tosis is primarily controlled by glutathione peroxidase 4 (GPX4).

33 oproteins, including antioxidant glutathione peroxidase 4 (GPX4).

34 lar antioxidant enzymes, such as glutathione peroxidase 4 (GPX4).

35 Intratumoral glutathione peroxidase 4 overexpression or acyl-CoA synthetase long

36 on was synthetically lethal with glutathione peroxidase-4 (GPX4) inhibition; GPX4 inhibition is a kno

37 educed levels of glutathione and glutathione peroxidase-4 (Gpx4), along with increased free iron, mit

38 ot in that induced by inhibiting glutathione peroxidase-4 (GPX4), the most downstream component of th

39 or beta(2B) subunits conjugated to ascorbate peroxidase(5) in mouse hearts, and use multiplexed quant

40 Here, we provide evidence that glutathione peroxidase 8 (GPX8), a poorly characterized enzyme that

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

42 The actual peroxidase activation step corresponds to subsequent sid

43 ssay suggests that this compact conformer is peroxidase active.

44 -client binding sites that are buried in the peroxidase-active protein.

45 lectron transport chain but transitions to a peroxidase-active state upon exposure to oxidative speci

46 superoxide dismutase, catalase and ascorbate peroxidase activities as compared to control.

47 cursor to engage both the cyclooxygenase and peroxidase activities of COX-2.

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

49 oxygenase/peroxygenase and reductant oxidase/peroxidase activities, and on reaction conditions, such

50 l soluble sugar, protein, catalase activity, peroxidase activity and increased in proline content, 2,

51 hosphomimetic Cytc had decreased cardiolipin peroxidase activity and is more stable in the presence o

52 re that SpAhpD exhibits weak thiol-dependent peroxidase activity and, unlike the previously reported

53 3b MbnH combined with spectroscopic data and peroxidase activity assays provided evidence that MbnH i

54 ble ABTS significantly affect the results of peroxidase activity assays.

55 erestingly, eukaryotic 2-Cys Prxs lose their peroxidase activity at high H(2)O(2) levels.

56 ons since 2013 and intends to understand the peroxidase activity in gold nanozymes with variable phys

57 to the proposed mechanisms for the intrinsic peroxidase activity in gold nanozymes.

58 xide scavenging effects, considering minimal peroxidase activity in this space.

59 amined the kinetics of the H(2)O(2)-mediated peroxidase activity of cyt c both in the presence and ab

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

61 sed by this design also enhances the nascent peroxidase activity of the protein-heme complex.

62 The peroxidase activity ultimately results in the release of

63 Since 2004, when peroxidase activity was reported for the first time in g

64 el Ce@IrNRs with large surface area and high peroxidase activity were synthesized to amplify the sign

65 a conformational change that switches on its peroxidase activity when it binds to CL-containing membr

66 researches have been done on assessing their peroxidase activity with changing morphology, and making

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

68 cations, stability, and possessing excellent peroxidase activity.

69 intracellular H(2)O(2) homeostasis via their peroxidase activity.

70 on in the induction and stimulation of cyt c peroxidase activity.

71 al membranes and ensuing inactivation of its peroxidase activity.

72 he mechanisms by which cyt c self-limits its peroxidase activity.

73 lipid cardiolipin (CL), leading to a gain of peroxidase activity.

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

75 are shown to possess significantly enhanced peroxidase activity.

76 trated here by resurrecting ancestral fungal peroxidases, after sequence reconstruction from genomes

77 faces pre-modified with enzymes (horseradish peroxidase, alkaline phosphatase and glucose oxidase) or

78 thione peroxidase-like enzymes and ascorbate peroxidase, all of which have cell compartment-specific

79 enzyme evolutionary distance from the first peroxidase ancestor.

80 ansfer rates also showed how the most recent peroxidase ancestors that already incorporated the expos

81 ctivity of the antioxidant enzymes catalase, peroxidase and ascorbate peroxidase was also increased a

82 ormed validation screens against horseradish peroxidase and carbonic anhydrase IX, and we developed a

83 activity of antioxidant enzymes (glutathione peroxidase and catalase).

84 yclaceae families, showed higher activity of peroxidase and cytochrome, and gave largest removal of O

85 In summary, SpAhpD is a weak peroxidase and does not transfer electrons to AhpC, and

86 ble alternatives to the two natural enzymes (peroxidase and glucose oxidase) realized through real sa

87 Of them, lgi-miR-317 and its targets peroxidase and lncRNA TCONS_00951105 are implicated in a

88 rase, phospholipid hydroperoxide glutathione peroxidase and peroxidase were significantly up-regulate

89 activity of superoxide dismutase, ascorbate peroxidase and phenylalanine ammonia-lyase.

90 s in EC barrier function through glutathione peroxidase and phospholipase A(2) activity.

91 ial count along with lower soluble quinones, peroxidase and polyphenol oxidase activities in contrast

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

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

94 e(III)OH) reduction potential in horseradish peroxidase and the two-electron compound I/ferric (or Fe

95 ronine (fT3, TT3), and autoimmunity [thyroid peroxidase and thyroglobulin antibodies (TPOAb and TgAb,

96 e and Rhodocyclaceae families, activities of peroxidases and cytochromes, and the degradation of OMPs

97 t PRX9 and PRX40 encode Arabidopsis extensin peroxidases and highlights the importance of extensin cr

98 DPH oxidases, peroxisomal oxidases, type III peroxidases and other apoplastic oxidases.

99 t the impurities inhibit the activity of the peroxidases and the influence varies for different batch

100 med between a redox metalloenzyme (ascorbate peroxidase) and its reducing substrate (ascorbate).

101 cytochrome P450 monooxygenase, cytochrome c peroxidase, and benzylsuccinate synthase (BSS).

102 ed expression of Siglec-F, CD11c, eosinophil peroxidase, and other markers typical for activated eosi

103 d enzymatic antioxidant markers (Glutathione peroxidase, and superoxide dismutase).

104 e due to moisture reduction, inactivation of peroxidase, and the short-duration of heating.

105 nti-thyroglobulin (anti-TG) and anti-thyroid peroxidase (anti-TPO) as models.

106 rates among euthyroid women who had thyroid peroxidase antibodies and a history of miscarriage or in

107 United Kingdom underwent testing for thyroid peroxidase antibodies and thyroid function.

108 Thyroid peroxidase antibodies are associated with an increased r

109 evothyroxine in euthyroid women with thyroid peroxidase antibodies did not result in a higher rate of

110 In patients who have circulating thyroid peroxidase antibodies, there is a greater risk of progre

111 hyronine (T3), free thyroxine (FT4), thyroid peroxidase antibody (Anti-TPO), and thyroid stimulating

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

113 talase, superoxide dismutase and glutathione peroxidase antioxidant enzyme activities but maintains g

114 by knocking in (KI) an engineered ascorbate peroxidase (APEX) gene to the endogenous locus of lysoso

115 In this study, we repurpose the engineered peroxidase APEX2 as the first genetically encoded marker

116 proximity proteomics approach employing the peroxidase APEX2 coupled with 2 known WPB-associated pro

117 echnique, APEX-seq, which uses the ascorbate peroxidase APEX2 to probe the spatial organization of th

118 used two approaches to target the engineered peroxidase APEX2 to specific cellular RNAs for RNA-cente

119 We used the ascorbate peroxidase (APEX2) proximity labeling system, which labe

120 ral enzymatic antioxidants such as ascorbate peroxidase (APX), catalase (CAT), superoxide dismutase (

121 m, suggesting a role for ascorbate-dependent peroxidase (APX), which degrades mitochondrial H(2)O(2)

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

123 to the substrate was higher than horseradish peroxidase as a natural enzyme.

124 of enzymes (glucose oxidase and horseradish peroxidase), as well as the ferrocyanide, mediator of th

125 To follow the pace of gold peroxidase (Auperoxidase) nanozyme based biosensing stra

126 Our multiplexed peroxidase-based EM labeling system should therefore gre

127 belongs to the bacterial diheme cytochrome c peroxidase (bCcP)/MauG protein family, and MbnP contains

128 nces in biomass, chlorophyll (p > 0.19), and peroxidase between BPA-treated and untreated plants indi

129 by secondary antibody-poly-HPR (horseradish peroxidase) bioconjugates containing 400 HRP enzyme labe

130 exhibits high selectivity 1:400 horse radish peroxidase/bovine serum albumin, sensitivity to 100 atto

131 we present the discovery of a unique diheme peroxidase BthA conserved in all Burkholderia.

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

133 in vivo-assembled, catalytically proficient peroxidase, C45, we have recently demonstrated the catal

134 c cycles of heme-containing enzymes (P-450s, peroxidases, catalases, and cytochrome c oxidase) involv

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

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

137 Cytochrome c peroxidase (CcP) employs a Trp191(*+) radical to oxidize

138 cturally nonhomologous protein, cytochrome c peroxidase (CcP), by only two mutations (Cu(A)CcP).

139 de (H(2)O(2)) respiration using cytochrome c peroxidase (Ccp).

140 ed tips from tryptic digests of horse radish peroxidase, chicken avidin, and human immunoglobulin G,

141 protein content, activities of catalase and peroxidase, chlorophyll and capsaicin content gradually

142 Earlier, we identified three peroxidase-coding genes from A. annua, whereby Aa547 sho

143 e iron(IV) oxo (or ferryl) form of ascorbate peroxidase compound II (APX-II) is a subject of debate.

144 istochemistry in Norway spruce buds based on peroxidase-conjugated antibodies and tyramide signal amp

145 parable to those of conventional horseradish-peroxidase-conjugated secondary antibodies, regardless o

146 talytic processing in individual horseradish peroxidase-containing Ru(4)PCVs, and chemical signalling

147 ence pathways other than H(2) O(2) burst and peroxidases contribute to the bsr-d1-mediated immunity.

148 tion of spermine, was coupled to horseradish peroxidase conversion of Amplex(R) Red (1-(3,7-dihydroxy

149 (2) detection is typically performed through peroxidase-coupled reactions utilizing organic dyes that

150 We identified the plastid ascorbate peroxidase (cpAPX) genes across angiosperms and analyzed

151 ), suggest that these monomers function as a peroxidase, distinct from the established MnSOD superoxi

152 It suggested cell growth, dye-decolorizing peroxidase (DyP) and reactive oxygen species (ROS) were

153 In dye-decolorising heme peroxidases (DyPs), controversy exists regarding the mec

154 e report the identification of two class III peroxidase-encoding genes, PEROXIDASE9 (PRX9) and PRX40,

155 n direct proximity labeling of RNA using the peroxidase enzyme APEX2.

156 atural antioxidants catalyzed by the soybean peroxidase enzyme was studied using uv-vis spectroscopy.

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

158 nate), is a common chromogenic substrate for peroxidase enzymes, which are widely used in biochemical

159 nophil cationic protein (ECP) and eosinophil peroxidase (EPO) (P < .05), while IFABP was positively r

160 3app) ) showed a progressive increase during peroxidase evolution (up to 50-fold higher values for th

161 tertiary structure homology modelling of the peroxidases for docking studies.

162 A class III peroxidase from Artemisia annua has been shown to indica

163 Immobilized dye-decolorizing peroxidase from Pseudomonas putida MET94 (PpDyP) and thr

164 odifications that accompany the onset of the peroxidase function are well-characterized.

165 This peroxidase function plays a key role during apoptosis.

166 hniques use a promiscuous biotin ligase or a peroxidase fused to a protein of interest, enabling the

167 , gene ontology functions, and the family of peroxidase genes.

168 ew years have witnessed a boom in the use of peroxidase gold nanozyme in biosensing applications.

169 itrosalicylic acid (DNS) and glucose oxidase/peroxidase (GOPOD) methods.

170 Measurements of plasma glutathione peroxidase (GPx) activity and serum selenium concentrati

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

172 in colostrum follows the order: glutathione peroxidase (GPX) ~ selenoprotein P (SELENOP) > selenocys

173 mycin (mTOR) for proliferation and the lipid peroxidase GPX4 for protection from ferroptosis of inner

174 Among the last group, glutathione peroxidases (GPxs) and peroxiredoxins (Prxs) are the mos

175 plications, such as ELISA tests based on the peroxidase-H(2)O(2)-ABTS system, should be carried out a

176 )OH(2)(Por)) reduction potential in aromatic peroxidase has allowed us to gauge the accuracy of theor

177 ioxidant enzymes, including catalase and GSH peroxidases, have supported a model in which beta-cells

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

179 Horseradish peroxidase (HRP) and hydrogen peroxide concentrations we

180 Horseradish peroxidase (HRP) as a model enzyme was co-assembled with

181 using streptavidin-conjugated to horseradish peroxidase (HRP) in the presence of luminol and H(2)O(2)

182 The inhibition of horseradish peroxidase (HRP) is uncompetitive for the substrate H(2)

183 bioreagents loaded with multiple horseradish peroxidase (HRP) molecules, recognizing the epimark in a

184 e cleavage cascade also released horseradish peroxidase (HRP) pre-attached to the amplification probe

185 aptamer, which was conjugated to horseradish peroxidase (HRP) through biotin-streptavidin binding.

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

187 n support the catalytic cycle of horseradish peroxidase (HRP) without the need of H(2)O(2) to be pres

188 silver nanoparticles (AgNPs) and horseradish peroxidase (HRP), altogether, formed the signaling probe

189 e, we used receptor mutagenesis, horseradish peroxidase (HRP), and ascorbate peroxidase 2 (APEX-2) pr

190 dings of various proteins (e.g., horseradish peroxidase (HRP), bovine hemoglobin, immunoglobulin G, a

191 ternary complex of T(30)-biotin/horseradish peroxidase (HRP)-biotin/streptavidin to the poly(A) tail

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

193 The insulin detection is based on a peroxidase (HRP)-labeled sandwich assay whereas the cort

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

195 ost at the same level as natural horseradish peroxidase (HRP).

196 ntibodies that were labeled with horseradish peroxidase (HRP).

197 randomly anchoring two pairs of horseradish peroxidase (HRP)/glucose oxidase (GOx) at the vertices o

198 unconjugated and conjugated with horseradish peroxidase (HRP)] onto magnetic microbeads (MBs) used as

199 secondary antibody labeled with horseradish peroxidase (HRP-DAb).

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

201 rrent views on the activities of thiol-based peroxidases in peroxide-mediated redox signaling process

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

203 peroxiredoxin (2-Cys PRX), a thiol-dependent peroxidase, in the control of the reducing activity of c

204 ting H(2)O(2) reduction with the glutathione peroxidase inhibitor, mercaptosuccinate, enhanced the H(

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

206 m viability, and a spermathecal-derived heme peroxidase is required for long-term Anopheles gambiae f

207 unctioned epistatically with the thioredoxin peroxidase Jafrac1 and the thioredoxin reductase 1 TrxR-

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

209 at do not require activation by the catalase peroxidase KatG, thus circumventing the majority of the

210 g nanobodies and then prepared a horseradish-peroxidase-labeled nanobody using a mild conjugation pro

211 The I immunosensor relies on a peroxidase-labeled sandwich immunoassay, while G is moni

212 zed by AChE, choline oxidase and horseradish peroxidase, leading to production of hydrogen peroxide,

213 ae infection and degradation of H(2) O(2) by peroxidases, leading to resistance to M. oryzae.

214 l label in the immunoassay due to their high peroxidase-like activity and low migration speed.

215 onally designed new nanohybrid with enhanced peroxidase-like activity and site-specific biorecognitio

216 Specifically, the average peroxidase-like activity of Mt nanoparticles after 72 h

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

218 fungal-mineral cultivation exhibit intrinsic peroxidase-like activity.

219 The Nanozyme Nest features amplified peroxidase-like catalytic ability from graphene and Fe-M

220 The resultant AuPt/ZIF-8-rGO shows enhanced peroxidase-like catalytic activity and it is applied for

221 complementary nucleic acid, sDz releases the peroxidase-like deoxyribozyme apoenzyme, which, in compl

222 oved by catalase, peroxiredoxin, glutathione peroxidase-like enzymes and ascorbate peroxidase, all of

223 In this study, we show that lignin peroxidase (LiP), an extracellular enzyme purified from

224 ellulase (CL), beta-glucosidase (BG), lignin peroxidase (LiP), and manganese peroxidase (MnP), but de

225 e calibration of the ancestry of Polyporales peroxidases localized the appearance of the first peroxi

226 ector that expresses the genetically encoded peroxidase marker for mitochondria, mito-APEX2, at the m

227 eactions detected the presence of eosinophil peroxidase, MBP, and fibrin alpha-, beta-, and gamma-cha

228 t and defence by its involvement in type III peroxidase-mediated polymer cross-linking, lignification

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

230 fic aptamer for CA125 as capture reagent and peroxidase mimetic gold nanoparticles as label for detec

231 y detects an analyte by using an aptamer and peroxidase mimetic gold nanoparticles that ensures circu

232 ctrodes for food analysis using nanozymes as peroxidase mimetics.

233 llic AuPt nanoparticles (AuPtNPs) as a novel peroxidase mimic for high-sensitivity detection of H(2)O

234 hest electronic current and showed excellent peroxidase-mimic towards H(2)O(2) using chronoamperometr

235 By exploiting the peroxidase-mimicking activity of AuNCs and the precise n

236 m nanozyme (SAN) that exhibits unprecedented peroxidase-mimicking activity.

237 ase-, superoxide dismutase-, and glutathione peroxidase-mimicking enzyme properties exhibit cytoprote

238 rporated magnetic graphene oxide (PMGO) as a peroxidase-mimicking nanozyme with high oxidizability to

239 ized chip (biochip(ApoA1)) and self-linkable peroxidase-mimicking, PB-incorporated magnetic graphene

240 viral vector with the mitochondria-targeting peroxidase mito-APEX2 and expressed it at the mouse caly

241 (BG), lignin peroxidase (LiP), and manganese peroxidase (MnP), but decreased laccase (LA) potential a

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

243 ers) as biospecific recognition elements and peroxidase or DNAzymes as chemiluminescence reporters.

244 l properties than PO, with lower activity of peroxidase (p = 0.004) and polyphenoloxidase (p = 0.001)

245 Here, we show that the thiol-specific peroxidase peroxiredoxin-4 (Prdx4) directly regulates IL

246 enzymes involved in this scavenging process, peroxidases play a crucial role, using NADPH provided mo

247 tathione (GSH) redox molecule and the enzyme peroxidase (PO), which were synthesized by Saccharomyces

248 mutase and significantly enhanced (p < 0.05) peroxidase (POD) activity contributed greatly to the det

249 perishability, the inactivation kinetics of peroxidase (POD) and polyphenol oxidase (PPO) were inves

250 57%) was obtained at 300 MPa x 3 pulses, and peroxidase (POD) enzymes (31%) at 600 MPa working in sta

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

252 talase (CAT), superoxide dismutase (SOD) and peroxidase (POD) in roots and shoots indicate a general

253 , reduced glutathione (GSH), catalase (CAT), peroxidase (POD), superoxide dismutase (SOD) and glutath

254 Using polymeric horseradish peroxidase (poly-HRP, 400 HRPs) labels to provide large

255 then capture streptavidin-poly [horse radish peroxidase] (Poly-HRP).

256 WKS1 phosphorylates the thylakoid ascorbate peroxidase protein and reduces its ability to detoxify p

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

258 Secreted enzymes, namely laccases (LACs) and peroxidases (PRXs), facilitate lignin polymerization by

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

260 The -O-O- linkage in artemisinin makes peroxidases relevant to its metabolism.

261 R Abs, with Abs to thyroglobulin and thyroid peroxidase remaining unchanged.

262 Bacterial diheme peroxidases represent a diverse enzyme family with funct

263 roperoxidases or cyt P450 monooxygenases and peroxidases, respectively.

264 ified by using Congo red and anti-eosinophil peroxidase staining.

265 with a commercial conjugate of streptavidin-peroxidase (Strep-HRP) as tracer.

266 However, these peroxidase substrates showed moderate to minimal inhibit

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

268 at is a member of the bacterial cytochrome c peroxidase superfamily, capable of generating a highly u

269 hysiological responses in catalase, guaiacol peroxidase, superoxide dismutase, soluble protein, ligni

270 Both oxidase and peroxidase systems could oxidize I(-) to I(2) or hypoiod

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

272 oxidase, 3,3',5,5'-tetramethylbenzidine, and peroxidase that detected concentrations up to 50.0 mmol

273 gen species and cytochrome c, a proapoptotic peroxidase that is released from mitochondria during sus

274 ate in lignin biosynthesis as a bifunctional peroxidase that oxidizes both ascorbate and 4-coumarate

275 Peroxidasin is a heme peroxidase that oxidizes bromide to hypobromous acid (HO

276 d on two kinds of redox chemistry, catalases/peroxidases that depend on the heme prosthetic group to

277 to afford peroxide reduction and thiol-based peroxidases that support their redox activities on speci

278 hibited GM-CSF-induced release of eosinophil peroxidase, TNF-alpha, and IL-8 (n = 7-8) but did not pr

279 ch with rapamycin-dependent targeting of the peroxidase to a protein of interest, we searched for pro

280 By targeting this enhanced peroxidase to different subcellular compartments, multip

281 two enzymes, alcohol oxidase and horseradish peroxidase, to correlate ethanol sweat concentrations to

282 an TCR specific for the self-antigen thyroid peroxidase (TPO) is positively selected in the thymus of

283 mality avail the templating of a horseradish peroxidase train, which boosted the paralleled catalytic

284 ng the antiferroptotic mediator, glutathione peroxidase type 4.

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

286 are dual-function proteins, either acting as peroxidases under non-stress conditions or as chaperones

287 It significantly reduced peroxidase value (POV) and thiobarbituric acid (TBA) val

288 t enzymes catalase, peroxidase and ascorbate peroxidase was also increased at harvest by SA and MeJA

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

290 pid hydroperoxide glutathione peroxidase and peroxidase were significantly up-regulated uniquely at 4

291 and k(3) involved in the catalytic cycle of peroxidases were calculated.

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

293 ular structure (as well as the extant lignin peroxidase) were comparatively more efficient at oxidizi

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

295 In this study, we report a Th-MOF artificial peroxidase, which can oxidize 3,3,5,5-tetramethylbenzidi

296 catalysts, similar to nanozymes that imitate peroxidase, which scavenges hydrogen peroxide for the mi

297 idases localized the appearance of the first peroxidase with a solvent-exposed catalytic tryptophan t

298 a the redox sensor, peroxiredoxin-1, a thiol peroxidase with high reactivity towards H(2)O(2) that ac

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

300 s associated with the appearance of secreted peroxidases with a solvent-exposed catalytic tryptophan.

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