ライフサイエンスコーパス: ionophore

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

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

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

4 using phorbol myristate actetate or calcium ionophore.

5 slowly in response to treatment with calcium ionophore.

6 of the system is determined by the employed ionophore.

7 on of oligomycin and titration with a proton ionophore.

8 ode, in addition to the lipophilic carbonate ionophore.

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

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

11 unoprecipitate in the presence of the Ca(2+) ionophore.

12 te or a mutant TonE were unresponsive to the ionophore.

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

14 ic actions by acting as a Cu/Zn chelator and ionophore.

15 polymeric membrane, this molecule acts as an ionophore.

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

17 aphthalenesulfonate as a protamine-selective ionophore.

18 eatures consistent with those of known metal ionophores.

19 porphyrins were found to function as neutral ionophores.

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

21 t are closely related to naturally occurring ionophores.

22 or ion exchangers as well as neutral carrier ionophores.

23 without the need for the development of new ionophores.

24 adopted in European Community for polyether ionophores.

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

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

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

28 s, but not PS120/NHE3 cells, with the Ca(2+) ionophore, 4-bromo-A23187 (0.5 mum): 1) inhibited NHE3 V

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

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

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

32 The calcium ionophore A23187 induced SFK phosphorylation in both wil

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

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

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

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

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

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

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

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

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

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

43 n stimulation of the CESS cells with calcium ionophore A23187.

44 4) (LTB(4)) when stimulated with the calcium ionophore A23187.

45 le exocytosis are induced by PMA and calcium ionophore A23187.

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

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

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

49 a veterinary anthelmintic with known proton ionophore activities, was identified as a potent and spe

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

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

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

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

54 The zinc ionophore activity was demonstrated by exploring the use

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

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

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

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

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

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

61 ponse to inflammatory agonists (e.g. calcium ionophore and ATP).

62 nonactin diastereoisomer that can act as an ionophore and has antibacterial activity.

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

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

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

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

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

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

69 ordinated environments provided by selective ionophores and biological ion channels/transporters of k

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

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

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

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

74 in which alpha-latrotoxin acts like a Ca(2+) ionophore, and (2) a Ca(2+)-independent mechanism with C

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

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

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 the gold surface abolishes the necessity of ionophore application.

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

85 New ionophores are essential for advancing the art of select

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

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

88 Ionophores are widely used ion carriers in ion selective

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

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

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

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

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

94 Ionophore-based ion selective optical nanosensors that o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

117 g of a green-fluorescing triazacryptand K(+) ionophore-Bodipy conjugate, coupled to dextran, together

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

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

120 es within the membranes, suggesting that the ionophores can function via either a charged or a neutra

121 Overexpression of BTN1 or the presence of ionophore carbonyl cyanide m-chlorophenil hydrazone (CCC

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

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

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

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

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

127 ndogenous esterified lipid stores by calcium ionophore (CI) calcimycin (A-23187).

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

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

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

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

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

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

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

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

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

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

138 For membranes of low ionophore concentration, the polymer affected the sensor

139 The use of higher ionophore concentrations removes the undesirable effect

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

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

142 Ionophore dietary supplements that inhibit rumen protozo

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

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

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

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

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

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

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

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

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

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

153 Ionophore-doped sensing membranes exhibit greater select

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 Furthermore, the ionophore gramicidin can be incorporated into the bilaye

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

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

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

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

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

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

178 Ionophore I-based ISEs were successfully applied for chl

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

180 FcepsilonRI, and can be activated by Ca(2+) ionophore in a manner independent of antigen stimulation

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

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

183 one such triazolophane as a halide-selective ionophore in poly(vinyl chloride) (PVC) membrane electro

184 Rh(III)-tetra(t-butylphenylporphyrin) as the ionophore in the presence of lipophilic cationic sites i

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

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

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

188 f nonprimed macrophages with ATP and calcium ionophore induced a rapid release of MV that were predom

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

190 effect on human 5-LOX activity but impaired ionophore-induced intracellular calcium increase and cal

191 ntrations, both LTRAs also inhibited calcium ionophore-induced leukotriene (leukotriene B(4) and leuk

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

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

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

195 Treatment with the calcium ionophore ionomycin resulted in increased GlcAT-I expres

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

197 static joints by the intra-articular Ca(2+) ionophore ionomycin, prostaglandin E(2), cAMP-raising ag

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

199 titutively active calcineurin or the calcium ionophore ionomycin.

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

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

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

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

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

205 for both ion exchangers and neutral carrier ionophores is also discussed.

206 2+ and K+ ionophores but not with individual ionophores is sufficient to induce efficient internaliza

207 al and evoked IK(ATP) by ionomycin, a Ca(2+) ionophore, is activated by CaMKII.

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

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

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

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

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

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

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

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

216 The ionophore nigericin also reduces cytosolic pH and induce

217 7 receptor channels, the exogenous bacterial ionophore nigericin, or the lysosomotropic agent Leu-Leu

218 n reactions in the carboxylic acid polyether ionophore nigericin.

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

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

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

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

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

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 evaluated to identify concentrations of the ionophore, plasticizer, and lipophilic additive that giv

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

252 sor of intracellular Zn(2+), and that Zn(2+) ionophores, such as CQ and ZnPy, activate TRPA1 by incre

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

254 All ionophores tested exhibit preferred selectivity toward n

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

256 by Streptomyces griseus ETH A7796 and is an ionophore that is selective for K(+) ions.

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

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

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

266 ophen complexes with Rh(III) are examined as ionophores to prepare nitrite selective polymeric membra

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

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

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

272 TF pathway inhibitor inhibition, and calcium ionophore treatment.

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

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

275 The addition of a Ca(2+) ionophore under TLo conditions reversed the pro-Th17 eff

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

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

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

279 ydrophobic-ion-like membrane defects and the ionophore valinomycin, which exhibit little membrane def

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

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

282 2+) treatment, along with a selective Zn(2+) ionophore, we show that transient elevations in intracel

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

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

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

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

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

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

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

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

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

292 binds to Na+, K+, Ca2+, and the unprotonated ionophore with binding constants of 10(3.5), 10(1.8), 10

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

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

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

296 and one of four fluorophilic Ag(+)-selective ionophores with one or two thioether groups were investi

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

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

299 the solvent displacement method using sodium ionophore X, BME-44, and ETH 1001 for sodium-, potassium

300 phore I, lipophilic ion-exchanger and sodium ionophore X, BME-44, and ETH 5234 for sodium, potassium,