ライフサイエンスコーパス: ionophore

1 by sperm (but twice that achieved by calcium ionophore).

2 c solvatochromic dye (SD), ion exchanger and ionophore.

3 aphthalenesulfonate as a protamine-selective ionophore.

4 ation of a 1:1 complex for a Na(+)-selective ionophore.

5 ) and a cation-sensitive membrane without an ionophore.

6 slowly in response to treatment with calcium ionophore.

7 of the system is determined by the employed ionophore.

8 on of oligomycin and titration with a proton ionophore.

9 ode, in addition to the lipophilic carbonate ionophore.

10 s and the molar ratio of ionic sites and the ionophore.

11 nduced by glucocorticoid (6-48 h) or calcium ionophore.

12 using phorbol myristate actetate or calcium ionophore.

13 e C3v binding pocket of the 18-crown-6 ether ionophore.

14 polymeric membrane, this molecule acts as an ionophore.

15 s were suitable for routine determination of ionophores.

16 adopted in European Community for polyether ionophores.

17 eatures consistent with those of known metal ionophores.

18 porphyrins were found to function as neutral ionophores.

19 l in modeling the size-selective behavior of ionophores.

20 t are closely related to naturally occurring ionophores.

21 exit their host cell when exposed to calcium ionophores.

22 without the need for the development of new ionophores.

23 (SAs), 12 fluoroquinolones, 6 macrolides, 2 ionophores, 2 diaminopyimidines, 1 aminocoumarin, and 1

24 low pH was markedly inhibited by the proton ionophore 4-(trifluoromethoxy)phenylhydrazone; BSP influ

25 y for inhibition of NHE3 activity by calcium ionophore 4-Br-A23187.

26 Application of the Ca(2+) ionophore A23187 (1 microM), to activate Ca(2+)-activate

27 f phorbol 12-myristate 13-acetate (PMA) plus ionophore A23187 (Io), which induces NFAT activation, in

28 The calcium ionophore A23187 also induced NOD-dependent signaling, a

29 l 12,13-dibutyrate together with the calcium ionophore A23187 also promoted ubiquitination and protea

30 The calcium ionophore A23187 induced SFK phosphorylation in both wil

31 Treatment with the calcium ionophore A23187 recapitulated the force-induced perinuc

32 h LPS followed by treatment with the calcium ionophore A23187 resulted in the formation of PGE2, 5-HE

33 f MM6 cells by phorbol myristate acetate and ionophore A23187, a perinuclear ring pattern was observe

34 ith bacterial lipopolysaccharide and calcium ionophore A23187, and biosynthesis was blocked by inhibi

35 osis by progesterone, but not by the calcium ionophore A23187, and elicited a concomitant reduction o

36 ys induced by five stimuli; PMA, the calcium ionophore A23187, nigericin, Candida albicans and Group

37 Treatment with the calcium ionophore A23187, which increases Ca(2+)-calmodulin bind

38 scular endothelial growth factor, and Ca(2+) ionophore A23187, which is corroborated in isolated perf

39 wing treatment of SW1353 with 0.5 muM Ca(2+) ionophore A23187.

40 anced by IKKgamma in the presence of calcium ionophore A23187.

41 holipase C delta-EGFP at the PM after Ca(2+) ionophore (A23187)-induced PI(4,5)P2 hydrolysis, followe

42 2(S)-HETE-LPC and 12(S)-HETE-LPE, in calcium ionophore (A23187)-stimulated murine platelets.

43 yl-leucylphenylalanine (fMLP), or the Ca(2+) ionophore, A23187.

44 cute coronary syndrome patients, and calcium ionophores abolished the observed differences in the adh

45 nsient incubation of mouse sperm with Ca(2+) ionophore accelerated capacitation and rescued fertilizi

46 method, we show that thrombin, collagen, or ionophore-activated human platelets externalize two phos

47 hat 8-OHQs have distinct metal chelation and ionophore activities.

48 rrelation between the chelation capacity and ionophore activity is demonstrated, thus underlining the

49 ient liposomal system for screening the zinc ionophore activity of a selected library consisting of t

50 The zinc ionophore activity was demonstrated as the capacity of p

51 The zinc ionophore activity was demonstrated by exploring the use

52 We measured the zinc Kd zinc ionophore activity, ability to restore zinc to purified

53 rtificially activated by exposure to calcium ionophore, after which PB2 is biopsied and collected wit

54 red with ISMs, each containing two different ionophores, allowing the simultaneous sensing of K and N

55 porous polypropylene membranes doped with an ionophore and a lipophilic cation-exchanger are used her

56 The anion ionophore and a lipophilic pH indicator are inkjet-print

57 h a liquid membrane cocktail containing both ionophore and additive dissolved in plasticizer.

58 d these podocytes temporarily with a Calcium Ionophore and facultatively with Latrunculin A, an inhib

59 tomatal closure, induced by exogenous Ca(2+) ionophore and malate, was shown to be inhibited by exoge

60 the FcepsilonRI or combination of Ca (2)(+) ionophore and phorbol ester.

61 nclusions using p-tertbutyl calix[4]arene as ionophore and polymeric matrix (polyvinyl chloride) have

62 cells are stimulated by the addition Ca(2+) ionophore and that cellular localization is dependent up

63 e stoichiometry of the complexes between its ionophore and the target and interfering ions.

64 he strong selective interactions between the ionophore and the target.

65 cept is established with lithium and calcium ionophores and accompanied by a response model that assu

66 d stoichiometries misguide the design of new ionophores and are likely to result in the formulation o

67 oviding valuable guidelines to the design of ionophores and carrier-based ion selective sensors.

68 IB, along with counter-screens that identify ionophores and membrane perturbors.

69 an elevation of the intralysosomal pH, since ionophores and proton pump inhibitors that dissipate the

70 sensor incorporates highly calcium-selective ionophores and two fluorescence indicators that act as s

71 demonstration, valinomycin was used as K(+) ionophore, and a good Nernstian response with a slope of

72 the SC-ISE, indicating that the plasticizer, ionophore, and lipophilic anion are spontaneously distri

73 MM6 cells was increased by stimulation with ionophore, and that this complex was formed to the same

74 nd evidence that MESM acts as a Mn-selective ionophore, and we observed that it has increased rates o

75 gments containing pH-sensitive fluorophores, ionophores, and ion-exchangers enable highly selective a

76 with covalently attached or freely dissolved ionophore- and ionic-liquid-doped reference membranes ca

77 and calcium influx; dithiocarbamate, a metal ionophore; and aluminum hydroxide (alum), an immunologic

78 ample is the biosynthesis of lasalocid A, an ionophore antibiotic polyether.

79 The veterinary ionophore antibiotics (IPAs) are extensively used as coc

80 Ionophore antibiotics (IPAs) are polyether antimicrobial

81 Ionophore antibiotics (IPAs) are polyether compounds use

82 Veterinary ionophore antibiotics (IPAs) are polyether compounds use

83 With continued ionophore application,TMEM16F-expressing cells then unde

84 the gold surface abolishes the necessity of ionophore application.

85 ing 1:1 stoichiometry) with their respective ionophores are calculated and agree well with the values

86 New ionophores are essential for advancing the art of select

87 +) transfers facilitated by highly selective ionophores are measured and analyzed numerically using t

88 lective electrodes (ISEs) containing neutral ionophores are used in clinical, industrial, and environ

89 Ionophores are widely used ion carriers in ion selective

90 Transmembrane ion transporters (ionophores) are widely investigated as supramolecular ag

91 ata identify salinomycin and other polyether ionophores as novel potential antiscarring therapeutics.

92 "water finger" prior to complexation with an ionophore at the membrane/water interface.

93 selectivities of the ionophore-free and the ionophore-based electrodes with 25 mol % and 71 mol % ca

94 edict experimental conditions for thin-layer ionophore-based films with cation-exchange capacity read

95 Ionophore-based ion selective optical nanosensors that o

96 thane (TCNQ) or its ion-radical salts and an ionophore-based ion-selective membrane.

97 hat the nanoparticles are among the smallest ionophore-based ion-selective nanosensors reported to da

98 We present here alternative, heterogeneous ionophore-based ion-selective nanospheres as indicators

99 sible to extend the redox buffer approach to ionophore-based ISEs.

100 ls in two independent cells lines through an ionophore-based mechanism, maintaining cell viability an

101 An initially nonpolarized ionophore-based membrane allows one to establish a net c

102 lcium pump based on a fast diffusive calcium ionophore-based membrane is reported.

103 l chloride), polystyrene, and poly(acrylate) ionophore-based membranes of the same thickness and comp

104 orward on ion discrimination with thin multi-ionophore-based membranes with thicknesses of 200 +/- 25

105 licability of the method is demonstrated for ionophore-based Mg(2+)-, Ca(2+)-, and Na(+)-selective el

106 haustive sensor concept is demonstrated with ionophore-based nanooptodes either selective for calcium

107 tammetric thin layer ( approximately 200 nm) ionophore-based polymeric films of defined ion-exchange

108 n important advantage of voltammetry with an ionophore-based polymeric membrane against the potentiom

109 of polypeptide protamine from water into an ionophore-based polymeric membrane has been hypothesized

110 mechanistically assess protamine transfer at ionophore-based polymeric membranes as foundation for re

111 rt that the voltammetric selectivity of thin ionophore-based polymeric membranes can be kinetically i

112 potentiometric and optical sensors based on ionophore-based polymeric membranes is thermodynamically

113 In contrast to photoresponsive ionophore-based systems, the concept presented here is a

114 We report on a plasticized polyurethane ionophore-based thin film material (of hundreds of nanom

115 dvancement of multi-ion detection with multi-ionophore-based thin films, polyurethane thin membranes

116 rt current pulse (5s) is applied between the ionophore-based working electrode and a biocompatible an

117 tural product (+)-SCH 351448, a macrodiolide ionophore bearing 14 stereogenic centers, is prepared in

118 ular [Zn(2+)]free by functioning as a Zn(2+) ionophore, binding Zn(2+) in the extracellular environme

119 ting cells with a combination of Ca2+ and K+ ionophores but not with individual ionophores is suffici

120 y, elevated Ca(2+) related (carbachol/Ca(2+) ionophore), but there was normal inhibition by forskolin

121 zed membrane typically contains an excess of ionophore, but lower than expected selectivities may be

122 ver calcium compared with two established Mn ionophores, calcimycin (A23187) and ionomycin.

123 ondrial dysfunction induced by mitochondrial ionophore, carbonyl cyanide m-chlorophenyl hydrazone and

124 Instead, we found that deltaT prevented ionophore-caused cytoplasmic membrane disruption, which

125 Ionomycin, a calcium ionophore, causes rapid mitochondrial accumulation of ac

126 se to mitochondrial perturbation by hypoxia, ionophore (CCCP) or doxorubicin.

127 In the presence of proton ionophores (CCCP, inhibitor of proton motive force), we

128 ported liquid membrane doped with a hydrogen ionophore (chromoionophore I), ion exchanger (KTFBP), an

129 nation of six antibiotics from the polyether ionophore class (lasalocid, maduramicin, monensin, naras

130 action and clean-up for the determination of ionophore coccidiostats in EU legislated foodstuffs, is

131 The resultant concentration of the Ca(2+)-ionophore complex in the ~1 mum-thick membrane can be at

132 oncentration of an aqueous analyte ion as an ionophore complex into the thin polymer membrane and is

133 try and overall formation constant of an ion-ionophore complex.

134 owered by the formation of a more stable ion-ionophore complex.

135 E mechanism to propose three-dimensional ion-ionophore complexation at the two-dimensional interface

136 ctrochemical (E) mechanism controlled by ion-ionophore complexation at the very interface in contrast

137 Selective ion-ionophore complexation in a polymeric membrane is crucia

138 Stability constants of the anion-ionophore complexes were determined from the dependence

139 An increase of the ionophore concentration in the membrane to 180 mM makes

140 t dissipating the membrane potential with an ionophore decreases the prevalence of the inward-facing,

141 se of MOSCs as a new class of size-selective ionophores dedicated to electrochemical sensing of molec

142 ion-selective membranes are formulated under ionophore depleted conditions (avoiding excess of ionoph

143 Ionophore dietary supplements that inhibit rumen protozo

144 nomycin and monensin, both monovalent cation ionophores, displayed a potent and selective cytotoxic e

145 , K-releasing agent (Gramicidin) and a metal ionophore (dithiocarbamate).

146 re, we report on the first application of an ionophore-doped double-polymer electrode for ion-transfe

147 prepare ion-selective electrodes (ISEs) with ionophore-doped fluorous sensing membranes.

148 The selectivities of ionophore-doped ion-selective electrode (ISE) membranes

149 ediate layer between a gold electrode and an ionophore-doped ISE membrane.

150 tivity over interfering ions as expected for ionophore-doped ISE membranes.

151 f insufficiently lipophilic species from the ionophore-doped ISMs into aqueous samples.

152 this approach, a approximately 1.6 mum thick ionophore-doped membrane contacts an aqueous solution co

153 loped a theoretical model for ITSV at a thin ionophore-doped membrane on the solid supporting electro

154 are quantitatively confirmed by using a thin ionophore-doped polymer membrane spin-coated on a conduc

155 ot only to confirm protamine extraction into ionophore-doped polymeric membranes but also to reveal p

156 Ionophore-doped sensing membranes exhibit greater select

157 directly on the solid substrate, and then an ionophore-doped solvent polymeric membrane was added in

158 Based on ionophore effects, we conclude that the Na(+) and H(+) t

159 After treatment with the Ca(2+) ionophore ETH129, which allows electrophoretic Ca(2+) up

160 pretreated with thapsigargin but not calcium ionophore exhibited increased Duox-1 mRNA expression.

161 r virtually any ion of interest for which an ionophore exists.

162 ed microfluidic device (muTAD) that includes ionophore extraction chemistry for the optical recogniti

163 etric data confirms that the dynamics of the ionophore-facilitated IT follows the one-step electroche

164 We reveal the slower ionophore-facilitated transfer of a smaller alkaline ear

165 y of the new cell to analyze both simple and ionophore-facilitated transfer of ions and proteins, pre

166 The mitochondrial proton ionophore, FCCP, caused a large, prolonged increase in c

167 The incorporation of a selective ionophore for carbonate allows one to determine this ani

168 calix[4]pyrrole-based molecule is used as an ionophore for the enhanced recognition of creatininium c

169 vorable, thereby requiring a Li(+)-selective ionophore for the ion-transfer mechanism.

170 used to demonstrate that a Ca(2+)-selective ionophore forms 1:3 and 1:2 complexes with calcium and m

171 nse slopes and unbiased selectivities of the ionophore-free and the ionophore-based electrodes with 2

172 To achieve this, we introduced previously ionophore-free ion exchanger membranes doped with a well

173 l-)(pot) = -3.71, as opposed to -0.36 for an ionophore-free ISE) and were optimized by adjusting the

174 , the high solubility of sample lipids in an ionophore-free sensing matrix results in a deterioration

175 on regeneration despite confirmed washout of ionophores from tissue.

176 lux in response to ionomycin, as a result of ionophore H2O2 sensitivity.

177 Salinomycin, an antibiotic potassium ionophore, has been reported recently to act as a select

178 d calcium ionophore IV (ETH 5234) or calcium ionophore I (ETH 1001).

179 ggest 1:1 complexation stoichiometry for the ionophore I with chloride as well as salicylate.

180 -based tris-urea bis(CF3) tripodal compound (ionophore I) were found to exhibit the best selectivity

181 Moreover, the ionophore I-based ISE membrane was shown to exhibit a ve

182 Ionophore I-based ISEs were successfully applied for chl

183 sing membranes composed of anionic sites and ionophore in a 1:4 molar ratio, which results in the for

184 K1/2 phosphorylation was increased by Ca(2+) ionophore in Par-C10 and HSY salivary cell lines.

185 merocyanine photoacid polymer and a calcium ionophore in plasticized poly(vinyl chloride).

186 to the amount of a Na(+)- or Li(+)-selective ionophore in thin polymeric membranes.

187 asticized PVC membranes containing up to two ionophores in addition to a lipophilic cation-exchanger,

188 nstrate that activation of TMEM16F by Ca(2+) ionophores in Jurkat T cells triggers large-scale surfac

189 es of p-tert-butylcalix[4]arene were used as ionophores in the development of solid-contact ion-selec

190 oth TgCDPK1 and TgCDPK3 were required during ionophore-induced egress, but only TgCDPK1 was required

191 We now show that a pulse of Ca(2+) ionophore induces fertilizing capacity in sperm from inf

192 tabilized by a lipophilic chloride-selective ionophore inside the membrane, while H(+) binds with the

193 In this study, using the calcium ionophore ionomycin and/or PMA on Jurkat T cells, we sho

194 phorbol 12-myristate 13-acetate, the Ca(2+) ionophore ionomycin, and the serine/threonine phosphatas

195 wn augmented necrosis mediated by the Ca(2+) ionophore ionomycin, whereas apoptosis mediated by the B

196 ransduction in vitro Conversely, the calcium ionophore ionomycin, which disrupts calcium gradients, b

197 titutively active calcineurin or the calcium ionophore ionomycin.

198 apid translocation was rescued by the Ca(2+) ionophore, ionomycin.

199 fluoride optode using an Al(III) -porphyrin ionophore is examined as an initial example of this new

200 iions at a thin polymeric membrane, where an ionophore is exhaustively depleted upon the transfer of

201 electrode based on a tweezer type carbonate ionophore is presented here for the first time.

202 h lithium ion (nJ = 1) by a Ca(2+)-selective ionophore is thermodynamically unfavorable, thereby requ

203 complexes of higher stoichiometry unless the ionophore is used in excess.

204 2+ and K+ ionophores but not with individual ionophores is sufficient to induce efficient internaliza

205 is(trifluoromethyl)phenyl]borate and calcium ionophore IV (ETH 5234) or calcium ionophore I (ETH 1001

206 greater extent than salinomycin, a potassium ionophore known to selectively inhibit CSCs.

207 d stoichiometry of the complexes between the ionophore, L, and the target and interfering ions (I (zi

208 n these results, Fc-PVC membranes doped with ionophores may form the basis of a new family of passive

209 Analyte-specific ionophore membranes are deposited on the surface of the

210 recent work, thin layer ion-selective multi-ionophore membranes can be interrogated by cyclic voltam

211 r a net charge of |zJ|/nJ - |zI|/nI for each ionophore molecule, which forms 1:nI and 1:nJ complexes

212 versely, activating the pump with the sodium ionophore monensin decreased burst frequency.

213 n with NHE6 or treatment with the Na(+)/H(+) ionophore monensin shifted APP away from the trans-Golgi

214 of exosome release through treatment with an ionophore, monensin, revealed a corresponding increase i

215 The ionophore nigericin also reduces cytosolic pH and induce

216 7 receptor channels, the exogenous bacterial ionophore nigericin, or the lysosomotropic agent Leu-Leu

217 n reactions in the carboxylic acid polyether ionophore nigericin.

218 ochondria was observed upon stimulation with ionophores, nigericin, or ionomycin.

219 the global elevation of [Ca(2+)]i by Ca(2+) ionophore or by Ca(2+) entry via ARC channels in native

220 rss31-null MCs were activated with a calcium ionophore or by their high affinity IgE receptors, they

221 al cells were stimulated by either a calcium ionophore or thapsigargin to produce NO.

222 er that can be rescued, in part, with Ca(2+) ionophores or agonists of TRPML1, a lysosomal Ca(2+) cha

223 ubber (SR), i.e. SR without any plasticizer, ionophore, or lipophilic anion, was applied on top of a

224 nes with platelet activating factor, calcium ionophore, or phorbol myristate acetate, develops within

225 nge properties and are doped with lipophilic ionophores originally developed for chemical ion sensors

226 hore depleted conditions (avoiding excess of ionophore over ion-exchanger), which is purposely differ

227 Functionally, spermatozoa exposed to calcium ionophore, phorbol ester, or H(2)O(2) exhibited superoxi

228 a general mechanism for epoxide selection by ionophore polyether epoxide hydrolases.

229 hibit no obvious interference from the other ionophores present in the membrane.

230 sicle membrane potential by agents including ionophores produce large changes of CQ accumulation that

231 ons in macrotetrolides, a class of polyether ionophores produced by Streptomyces species, was investi

232 ization assays suggest that 4 acts as a K(+)-ionophore, provided that the glycine carboxyl group is a

233 nhibitors (uncouplers), which are not simply ionophores, provided new insights into the enzyme mechan

234 veral metal-binding compounds, including the ionophore pyrithione zinc (PZ), that effectively inhibit

235 ally identify different classes of polyether ionophores rapidly and selectively.

236 and were optimized by adjusting the site-to-ionophore ratio to achieve the highest CN- selectivity,

237 predicted by established theory, the site-to-ionophore ratios that provide optimum potentiometric sel

238 ith the cADPR analog 3-deaza-cADPR or Ca(2+) ionophores recapitulated the effects of NAD(+) on TGF-be

239 lecular level mechanism of heterogeneous ion-ionophore recognition at plasticized polymer membrane/wa

240 SUPRAS-RAM efficiently extracted the ionophores (recoveries in milk, eggs, fat, liver, kidney

241 Both sodium and proton ionophores reduced ATP synthesis in the wild type grown

242 a related pathway for NET induction, whereas ionophores require an alternative pathway but that NETs

243 ation of VSM cells with ionomycin, a calcium ionophore, resulted in activation of CaMKIIdelta2 and Fy

244 and interact with ligand acting as a charged ionophore, resulting in Nernstian potentiometric respons

245 We discovered that the polyether ionophore salinomycin potently inhibited the formation o

246 he receptor is an optically silent uncharged ionophore selective for the analyte cation.

247 ol % and 71 mol % cationic sites relative to ionophore showed that the Zn(II) tetraphenylporphyrin fo

248 metric ion sensing system based on selective ionophores, specifically for the carbonate anion.

249 ncrease and/or LTB(4) formation triggered by ionophores, sphingosine 1-phosphate, and lysophosphatidi

250 In ionophore-stimulated (A23187; 1-2.5 muM) human blood neu

251 d good in vivo pharmacodynamics in a calcium ionophore-stimulated rat model after oral dosing (in viv

252 generate leukotriene (LT) C(4) upon calcium ionophore stimulation but had little effect on LTB(4) ge

253 o and in humans to phorbol ester and calcium ionophore stimulation in vitro in the face of low-dose R

254 luorous membranes doped with these carbonate ionophores suggests their use not only for potentiometri

255 n ion-transfer mechanism utilizes the second ionophore that independently transfers the secondary ion

256 We observed that PZ both acts as an ionophore that promotes uptake of toxic metals and inhib

257 ts a new paradigm for the rational design of ionophores that can rapidly and precisely monitor molecu

258 Ionophores that dissipated the membrane potential (Delta

259 ltiple such waves are observed with multiple ionophores that exhibit no obvious interference from the

260 ilitate the development of new ISEs based on ionophores that form complexes of higher stoichiometries

261 ISEs based on the most selective of the four ionophores, that is, 1,3-bis(perfluorodecylethylthiometh

262 g the scan of a membrane containing multiple ionophores, the least bound ion is expelled first, givin

263 the sample-ISM interface, from one to three ionophores, therefore promoting a change in the nature a

264 ieved to rely solely on its role as a proton ionophore; thus, the impact of each of its biological ac

265 ne is doped with a Na(+)- or Li(+)-selective ionophore to detect not only the primary ion, but also t

266 in composition except for the addition of an ionophore to one of the membranes.

267 where both ions form 1:1 complexes with the ionophores to transfer a net charge of +1.

268 ne (cAMP activator), and ionomycin (a Ca(2+) ionophore) to tissue-engineered constructs for 1 hour da

269 t, K(ILn), is not sufficiently large and the ionophore-to-ionic site ratio does not markedly exceed n

270 tiometric selectivities as a function of the ionophore-to-ionic site ratio or from calculations of co

271 n interfering ion is shown here to shift the ionophore-to-ionic site ratio that provides the highest

272 ities can be optimized by selection of ideal ionophore-to-ionic site ratios, considering complex stoi

273 n of intracellular chloride concentration by ionophores transiently decreased ATP production by mitoc

274 hagocytose apoptotic lymphocytes and calcium ionophore-treated erythrocytes but had no effect on ameb

275 the rapid resolution of thrombi produced by ionophore treatment of the mesenteric venules and reduce

276 TF pathway inhibitor inhibition, and calcium ionophore treatment.

277 Treatment with Ca(2+) ionophore triggers the association of AnxA2 with the spe

278 toward copper ions, much higher than that of ionophores typically used to induce selectivity for poly

279 However, the ionophores used in this study give examples of charges a

280 A valuable analog of the K(+)-ionophore valinomycin (1), bearing a pentafluorophenyl e

281 mple, K(+)-selective electrodes based on the ionophore valinomycin exhibit electrode-to-electrode sta

282 ride, the CFTR agonist genistein or the K(+) ionophore valinomycin.

283 cal application, a membrane containing three ionophores was used to determine lithium, sodium, and po

284 2+) treatment, along with a selective Zn(2+) ionophore, we show that transient elevations in intracel

285 Unfortunately, ionophores were found to promote the loss of insufficien

286 as reactive oxygen species (ROS) and calcium ionophore, whereas knockdown of RIP3 and MLKL blocked on

287 ed by the physiochemical properties of Cl(-) ionophores which have caused poor stability, drift, slug

288 firmed using valinomycin as a K(+)-selective ionophore, which forms a approximately 60 times more sta

289 he carbonate ion by a molecular tweezer-type ionophore, which has previously been demonstrated to exh

290 ically observed with another Na(+)-selective ionophore, which was assumed to form only a 1:2 complex

291 binding is augmented by a covalently grafted ionophore, while binding of other metals is prevented by

292 metry will emerge, and the membrane with the ionophore will exhibit a larger phase-boundary potential

293 Moreover, the use of this ionophore with a linear perfluorooligoether as membrane

294 Nigericin, another potassium ionophore with activity against cancer stem cells, exert

295 double-polymer membrane is facilitated by an ionophore with high Ca(2+) affinity and selectivity.

296 tochondria were depolarized on chip using an ionophore with results showing that the organelle viabil

297 Four ionophores with different selectivities toward Na(+), K(

298 the formation constants between the ions and ionophores with temperature.

299 Na(+),K(+)-ATPase (NKA) to monensin, a Na(+) ionophore, with and without ouabain, an NKA inhibitor, i

300 fying v-AuNW electrodes with polyaniline, Na ionophore X, and a valinomycin-based selective membrane,