ライフサイエンスコーパス: ferricyanide

1 nown electron acceptors, benzyl viologen and ferricyanide.

2 cyte lysates treated with an oxidant such as ferricyanide.

3 et state of rose bengal and its quenching by ferricyanide.

4 ytochrome by semidehydroascorbate but not by ferricyanide.

5 electrode (1-mm diameter) in the presence of ferricyanide.

6 but was inhibited at high concentrations of ferricyanide.

7 found to refold partially on oxidation with ferricyanide.

8 th for the reduction of biotin sulfoxide and ferricyanide.

9 -isoprostane formation due to extravesicular ferricyanide.

10 tochrome c, 2,6-dichlorophenolindophenol, or ferricyanide.

11 f intravesicular ascorbate by extravesicular ferricyanide.

12 ion containing the redox marker ferrocyanide/ferricyanide.

13 ive coupling species in situ using potassium ferricyanide.

14 and increase in peak splitting for potassium ferricyanide.

15 rons from intracellular Asc to extracellular ferricyanide.

16 antioxidant properties of vitamin C against ferricyanide.

17 2p to carry the NADPH-dependent reduction of ferricyanide.

18 the paramagnetic broadening agent potassium ferricyanide.

19 osed to a trans-membrane oxidant stress from ferricyanide.

20 xidized by either hydrogen peroxide, air, or ferricyanide.

21 +) form by treatment with a 3-fold excess of ferricyanide.

22 uction of the artificial electron acceptors: ferricyanide, 2,6-dichloroindophenol, 3-acetylpyridine a

23 Ferricyanide, 2,6-dichlorophenolindophenol, several quin

24 nd partially inhibited by myxothiazol (58%), ferricyanide (28%), and dithiothreitol (81%).

25 , largely superoxide dismutase-independent), ferricyanide (470 min(-1)), and other electron acceptors

26 Co-administration of AS with ferricyanide, a one-electron oxidant that converts NO(-)

27 Addition of ferricyanide, a strong oxidant, to the oxidized complex

28 ide reduction kinetic analysis (variation of ferricyanide absorption with time), much more sensitive

29 NADH:ferricyanide activity was 219 +/- 9.7 mumol/min/mg by us

30 al complex did not impair decyl-plastoquinol-ferricyanide activity.

31 the kinetics of NO release before and after ferricyanide addition in tissue homogenates to mathemati

32 T, test cells were treated with drugs before ferricyanide addition; cell counts from the amperometric

33 , the mass-transport controlled reduction of ferricyanide, allows for a proof of principle evaluation

34 Ferricyanide also generated dehydroascorbic acid that ac

35 uring purification and to use both potassium ferricyanide and 2,6-dichloroindophenol as electron acce

36 dditionally, two unpoised systems (potassium ferricyanide and ascorbic acid) were studied to evaluate

37 Dual wavelength analysis at 405 (ferricyanide and biomass) and 550 nm (biomass), allowed

38 and flow modes were evaluated using aqueous ferricyanide and compare favorably to those reported pre

39 from MoR, has similar kinetic properties for ferricyanide and cytochrome c reductase activities and v

40 sures of flavin and heme reduction kinetics, ferricyanide and cytochrome c reduction, and NO synthesi

41 +/CaM, as measured by reduction of potassium ferricyanide and cytochrome c.

42 resuspension, incubation in the presence of ferricyanide and finally ferrocyanide amperometry in dru

43 nd-order rate constants for the reactions of ferricyanide and oxygen.

44 We have found that ferricyanide and pentacyanoaminoferrate can be used as e

45 ity of the electrodes using the test analyte ferricyanide and perform recordings of quantal exocytosi

46 A combination of the electron acceptor, ferricyanide and the DeltapH indicator, 9-aminoacridine,

47 phenol-indophenol, 2) the iron (III) complex ferricyanide, and 3) the keto-acids oxaloacetate and pyr

48 side was inhibited by nitroblue tetrazolium, ferricyanide, and diphenyliodonium.

49 ed by the presence of nitroblue tetrazolium, ferricyanide, and diphenyliodonium.

50 in that reduces cytochrome c, methemoglobin, ferricyanide, and molecular oxygen in vitro.

51 he pH response while quinhydrone, ferro- and ferricyanide, and sodium sulfide have marked effects.

52 oactive potassium ferrocyanide and potassium ferricyanide, and supporting electrolyte, potassium chlo

53 and Lys-146 were much more accessible to the ferricyanide anion in the apoE3.DMPC complex than in the

54 of the substrates cytochrome c and potassium ferricyanide approximately 100-fold, while substitution

55 The purified enzyme also utilized ferricyanide as an artificial electron acceptor, which e

56 s typically been studied using extracellular ferricyanide as an electron acceptor.

57 metric analysis was performed with potassium ferricyanide as an electron mediator under argon or atmo

58 The A129T MSR mutant transfers electrons to ferricyanide as efficiently as wild type MSR but the rat

59 l pulse voltammetries using the ferrocyanide/ferricyanide as redox probe.

60 t SOR or SOO activities with ferrocyanide or ferricyanide as the redox partners.

61 The enzyme exhibited Nr activity via ferricyanide assay.

62 is-light electron generating system, reduces ferricyanide at a rate of 1.8 mumol/min/ nmol reductase.

63 inone was unusually insensitive to oxygen or ferricyanide at pH 8 and showed absorbance peaks at 372

64 ase domain of CYPOR reduced cytochrome c and ferricyanide at rates 2-fold higher than that of native

65 N-bound reductase catalyzes the reduction of ferricyanide at rates of 0.43 and 0.28 mumol/min/ nmol r

66 A ferricyanide-based electrochemical cell respiration assa

67 tive chemiluminescence in conjunction with a ferricyanide-based hemoglobin oxidation assay to prevent

68 Indeed, a ferricyanide-based spectrophotometric assay revealed tha

69 cts were blocked by myoglobin oxidation with ferricyanide but not by the xanthine oxidoreductase inhi

70 ocyanide by O(2) as well as the reduction of ferricyanide by O(2).

71 Oxidation of the (abcd)4 complex with ferricyanide causes complete dissociation of chain d fro

72 icted by the Beer-Lambert law for a range of ferricyanide concentrations from 0.005 to 0.3 mM and sho

73 from Ludox, ferrocenemethanol and potassium ferricyanide diffused at rates identical to that measure

74 ghosts with the membrane-impermeant oxidant ferricyanide doubled the ghost membrane concentration of

75 ed to quantitatively detect the reduction of ferricyanide down to a concentration of approximately 10

76 Oxidant (ferricyanide) electrochemically dosed at small rates (<o

77 Ferricyanide electrochemistry is totally inhibited on gr

78 a recently described modified assay using a ferricyanide-enhanced reaction mix at biologically relev

79 CN)6]K4, ferric tacn [Fe(III)(tacn)2]Br3 and ferricyanide [Fe(III)(CN)6]K3.

80 the proof-of-concept experiments described, ferricyanide, Fe(CN)6(3-), was produced by the transport

81 sed one-electron transfer systems (potassium ferricyanide/ferrocyanide and ferrous/ferric ammonium su

82 e anodic inlet and another drop of potassium ferricyanide for cathodic reaction flowed through patter

83 of contrast with osmium tetroxide/potassium ferricyanide, for BSE imaging, for the preparation and p

84 sulfite followed by partial reoxidation with ferricyanide generates an EPR spectrum with g-values sim

85 edox couple potassium ferrocyanide/potassium ferricyanide (HCF).

86 blood when MetHb formers, such as potassium ferricyanide, hydroxylamine, sodium nitrite, and 4-dimet

87 ial recovery of enzyme activity by potassium ferricyanide illuminated an alternative irreversible mec

88 tic activity do not support the reduction of ferricyanide in the Tris-light system in the absence of

89 on acceptors (molecular oxygen, APAD(+), and ferricyanide), in the presence and absence of a competit

90 h potential oxidant, such as cytochrome c or ferricyanide, in the presence of phospholipid vesicles o

91 Oxidation of the C199HT enzyme with ferricyanide increases the amount of the 3Fe cluster by

92 ate resealed within ghosts protected against ferricyanide-induced oxidation of endogenous alpha-tocop

93 mmol/L nitroblue tetrazolium and 0.1 mmol/L ferricyanide) inhibited pulmonary artery relaxation to n

94 us selectivity and sensitivity of the nickel ferricyanide interface is proposed.

95 ricyanide to the assay buffer; the effect of ferricyanide is attributed to oxidation of H2O2-dismutat

96 Potassium ferricyanide is known to oxidize ferrous sGC to the ferr

97 tro-oxidation of ferrocyanide, produced when ferricyanide is reduced by bacterial electron-transport.

98 A double mediator system is used in which ferricyanide is the final electron acceptor (the reporte

99 F-kappaB activation by hydrogen peroxide and ferricyanide, it had no effect of tumor necrosis factor-

100 Oxidation of RumA by ferricyanide leads to loss of the 390-nm band and appear

101 Reoxidation to Mo(V) by ferricyanide leaves bound sulfate trapped at the active

102 d biomass) and 550 nm (biomass), allowed for ferricyanide monitoring without interference of biomass

103 ucing power activity assessed with potassium ferricyanide of sheep whey protein was 1.3mg/ml.

104 ical signals from a soluble redox indicator, ferricyanide, on nitrocellulose films treated by cellula

105 f the nNOS heme or cytochrome c, but not for ferricyanide or dichlorophenolindolphenol, and establish

106 n acceptors, methyl viologen (MV), potassium ferricyanide, or dichloroindophenol.

107 sitive to oxygen, and ferric sGC prepared by ferricyanide oxidation has a 5c high-spin heme complex.

108 Ferricyanide oxidation of anaerobically reconstituted c-

109 Ferricyanide oxidation of the C415A mutant yielded a spe

110 ster using conventional methods of oxygen or ferricyanide oxidation or thiol exchange were not succes

111 By analogy with the properties of the ferricyanide-oxidized [4Fe-4S] cluster in Azotobacter vi

112 EPR spectra of ferricyanide-oxidized RumA show a fraction (<8%) of the

113 is estimated from a dithionite-reduced-minus-ferricyanide-oxidized spectrum.

114 The electrochemistry of a ferro/ferricyanide probe was used to characterise the TnT MIP

115 The reduction current of ferricyanide, product of the enzymatic reaction, is meas

116 eptors such as 2,6-dichlorophenolindophenol, ferricyanide, quinones, and molecular oxygen (O(2)).

117 rea of electrodes becoming accessible to the ferricyanide reaction after nitrocellulose digestion by

118 g a change in the reaction kinetics of ferro-ferricyanide redox couple at the electrode upon hybridiz

119 (SWV) reduction peak signal of ferrocyanide/ferricyanide redox couple due to the removal of the nega

120 l change alters the access of a ferrocyanide/ferricyanide redox couple to the aptasensor surface.

121 increase in reaction impedance for the ferro-ferricyanide redox couple.

122 ation resulted in a suppression of the ferro/ferricyanide redox current.

123 ation resulted in a suppression of the ferro/ferricyanide redox process.

124 posome-treated cells completely restored the ferricyanide-reducing capacity of the ghosts.

125 he effects of viscosogen on cytochrome c and ferricyanide reductase activities of holo-NaR and ferric

126 xhibited a low level of the cytochrome c and ferricyanide reductase activities, which either did not

127 had slower NADPH-dependent cytochrome c and ferricyanide reductase activities, which were associated

128 All four mutants showed decreased NADH:ferricyanide reductase activities, with kcat decreasing

129 A high ferricyanide reductase activity (indicative of NADH:cyto

130 ed antibody immunoprecipitated both the NADH-ferricyanide reductase activity and NADH-coenzyme Q(0) r

131 The FAD domain retains a high level of ferricyanide reductase activity but no cytochrome c redu

132 Whereas an NADH:ferricyanide reductase activity is evident in open membr

133 cyanide reductase activities of holo-NaR and ferricyanide reductase activity of the recombinant molyb

134 Ferricyanide reductase activity was unaffected, indicati

135 thracycline antitumor agents and a candidate ferricyanide reductase for plasma membrane electron tran

136 ly lower (<or=1000x) cytochrome c reductase, ferricyanide reductase, and NADPH oxidase activities tha

137 uctase activity but not the activity of NADH-ferricyanide reductase.

138 NH2-FAD, and riboflavin, are able to support ferricyanide reduction at a rate of 0.40, 0.52, 0.87, an

139 -reconstituted FMN-bound reductase catalyzes ferricyanide reduction at a rate of 1.1 mumol/min/nmol r

140 reductase in this system is able to catalyze ferricyanide reduction at a rate of 1.6 mumol/ min/nmol

141 1412D nNOS catalyzed faster cytochrome c and ferricyanide reduction but displayed slower steady-state

142 NADPH oxidation, cytochrome c reduction, and ferricyanide reduction by full-length eNOS or its isolat

143 Ferricyanide reduction kinetic analysis (variation of fe

144 sed on dual wavelength analysis of bacterial ferricyanide reduction kinetics is presented, using Esch

145 mbrane during the resealing step, subsequent ferricyanide reduction was enhanced.

146 Ferricyanide reduction was unaffected by cav-1P in all c

147 s measured indirectly as ascorbate-dependent ferricyanide reduction, correlated with the content of a

148 influence eNOS oxygenase domain function or ferricyanide reduction, it does potentiate the ability o

149 membrane content of alpha-tocopherol and in ferricyanide reduction.

150 ive titrations with dithionite and potassium ferricyanide, respectively, show that FAD is the only re

151 Reoxidation of the ferrous enzyme with ferricyanide results in alleviation of inhibition.

152 esponse of redox active molecules (potassium ferricyanide, ruthenium(III) hexammine, and ferrocene me

153 um or heparinized blood containing potassium ferricyanide showed ideal voltammetry while significant

154 Shift reagent experiments with potassium ferricyanide showed that Lys-143 and Lys-146 were much m

155 The color is not restored by ferricyanide, showing that the protein is modified irrev

156 molecular recognition element, and the ferro/ferricyanide solution as a redox probe, was developed.

157 was evaluated by measuring the absorbance of ferricyanide solutions at 420 nm.

158 een demonstrated via measurements on aqueous ferricyanide solutions using sample volumes as low as 20

159 sarcoplasmic reticulum (visualized by osmium ferricyanide staining of thin tissue sections), which su

160 Ferricyanide-stimulated ascorbate recycling from dehydro

161 H, Q-1, and the artificial electron acceptor ferricyanide strongly support an electron transport path

162 s the pi-back-bonding features in ferro- and ferricyanide that are significantly more intense in L-ed

163 After oxidation of the haem with ferricyanide, the absorbance spectrum of the reduced cyt

164 pair, and with the weak one-electron oxidant ferricyanide, the OG nucleoside reactivity is >6000-fold

165 Ferricyanide titration showed that the C415A mutant cont

166 ials down to -650 mV, but can be oxidized by ferricyanide to an S = 1/2 [4Fe-4S]3+ state (g = 2.09, 2

167 ar spin I = 3/2), followed by reoxidation by ferricyanide to generate the Mo(V) state of the active c

168 but was completely suppressed by adding 5 mM ferricyanide to the assay buffer; the effect of ferricya

169 Ferricyanide, tris(2,2'-bipyridine) ruthenium(II) chlori

170 The protein is fully capable of reducing ferricyanide, using NADPH as the electron donor.

171 Ferricyanide voltammetric responses correlate with the i

172 The Michaelis constant (K(M)) value for ferricyanide was 0.86 mM.

173 Using a small-molecule-based screen, ferricyanide was identified as a mild and efficient oxid

174 ochrome c, 2,6-dichlorophenolindophenol, and ferricyanide was inhibited by the addition of any of the

175 and nearly wild-type activity at pH 7.0 when ferricyanide was the electron acceptor.

176 Ferricyanide was used as an alternative electron accepto

177 Ferricyanide was used both to induce oxidant stress acro

178 rometry whereas the product of the reaction (ferricyanide) was recorded by absorbance.

179 Using the electron acceptor ferricyanide, we found that recombinant p67PHOX from bac

180 constant-potential electrolysis of potassium ferricyanide were used to characterize this rotating sam

181 releases NO at neutral pH in the presence of ferricyanide when reacted with an Fe(III) ligand like az

182 ponses at cathodic peak (+0.2V) of potassium ferricyanide, whereas pyruvate concentration was determi

183 cal impedance spectroscopy with ferrocyanide/ferricyanide, which revealed a very low charge-transfer

184 The FLDR reduces potassium ferricyanide with a kcat of 1610.3 min(-1) and a Km of 2

185 Erythrocytes reduced ferricyanide with generation of intracellular ascorbate

186 ata of cyclic voltammetry with 1mM potassium ferricyanide) with respect to conventional electrodes te

187 The presence of electrogenerated ferricyanide within the resulting evanescent field, beyo