ライフサイエンスコーパス: acidified

1 S stained intensely for the vATPase and were acidified.

2 ce of Na+ and HCO3(-), even when the soma is acidified.

3 ttenuated H37Ra strain acquired v-ATPase and acidified.

4 btained from the patients with MLIV are over-acidified.

5 not fuse with lysosomes and are only mildly acidified.

6 ely open, the cytosol of sour taste cells is acidified.

7 laque was centrifuged to yield plaque fluid, acidified (0.1 microL of 0.5 mol/L HCl per milligram pla

8 ctrospray ionization (ESI) of ubiquitin from acidified (0.1%) aqueous solution produces abundant ubiq

9 fast UHPLC separation (5min separation using acidified 10% MeOH isocratic flow in a CORTECS C18 colum

10 d-receptor complexes were disrupted using an acidified 10% methanol solution.

11 g DNA in positive ion mode is reported using acidified 3-hydroxypicolinic acid.

12 tively alkaline surface pH (4.3 +/- 0.1) was acidified (3.6 +/- 0.2) by indomethacin, and subsequent

13 long and 5 mm diameter) and then eluted with acidified 5 M NaCl solution directly into a sodium aceta

14 The acidified 70% acetone was identified as the ideal solven

15 sted samples and haem Fe was extracted using acidified 80% acetone for 60 min.

16 Extraction was performed with acidified acetonitrile (acetic acid 1% (v/v)), and addit

17 includes a prior protein precipitation with acidified acetonitrile for all samples and an additional

18 Extraction was performed with acidified acetonitrile, followed by a cleanup step with

19 in pfk2Delta, and the vacuolar lumen was not acidified after reassembly.

20 rsely, expressing ATP12A in CF mouse airways acidified airway surface liquid, impaired defenses, and

21 H(+)/K(+) adenosine triphosphatase (ATP12A) acidified airway surface liquid, which impaired airway h

22 n procedures through the reaction of Si with acidified ammonium molybdate, followed by precipitation

23 This effect is demonstrated by exposing acidified ammonium sulfate particles to 250 parts per bi

24 tion domain) as the lumen of the endosome is acidified and 2) low pH, in conjunction with acidic lipi

25 Milk samples were initially acidified and centrifuged, and then the supernatant was

26 Some endocytic vesicles were acidified and colocalized with LysoTracker.

27 d instead accumulate small vesicles that are acidified and contain the vacuolar proteins alkaline pho

28 The reaction mixture was then acidified and heated to induce stereospecific eliminatio

29 uently, vesicles can be locally recycled, re-acidified and re-used.

30 ltasecA2 mutant of M. tuberculosis were more acidified and showed greater association with markers of

31 with phagocytosis because phagosomes become acidified and the average fluorescence lifetime of EGFP

32 The milks were subsequently acidified and the distribution of protein between colloi

33 pbo-4 mutants the extracellular space is not acidified and the muscles fail to contract.

34 Urine was acidified and the organic acids were extracted by revers

35 whole blood was added to the sample chamber, acidified, and the HCN gas evolved was actively transfer

36 when pyrophosphate was added, the organelle acidified, and the rate of Ca(2+) uptake increased.

37 es were subjected to alkaline hydrolysis and acidified, and total (free + esterified) 15-PGFs and AA

38 The method involved mixing sample with acidified aqueous acetonitrile, followed by salt-out liq

39 brils upon incubation at room temperature in acidified aqueous solution at peptide concentrations >10

40 ions is produced by nanoESI from a slightly acidified aqueous solution with the micron outer diamete

41 Acidified aqueous solutions containing unfolded proteins

42 Adding glycerol to acidified aqueous solutions of cytochrome c shifts the m

43 Under basal conditions, CF epithelia acidified ASL more rapidly than NL epithelia.

44 ain-sensitive (nongastric) H+,K+-ATPase that acidified ASL, but its activity was not different in NL

45 a(+)/H(+) exchanger, intracellular pH in hTE acidified at significantly higher rates than in Calu-3,

46 orter of acidified mitochondria reveals that acidified axonal mitochondria originating from the retin

47 fects of 5-HT and halothane were examined in acidified bath solutions that blocked TASK channels.

48 act with early and late endosomes and become acidified before the onset of phagosomal disruption.

49 experiments to determine whether exposure to acidified bile salts causes esophageal epithelial cells

50 Exposure of squamous cells to acidified bile salts significantly increased the secreti

51 ophageal squamous cell lines were exposed to acidified bile salts to evaluate their effects on cytoki

52 at addition of moderate amounts of pepsin to acidified bovine insulin at close to physiological tempe

53 Solution chemistry indicated that CO(2)-acidified brine preferentially dissolved dolomite until

54 nt with an experimental study in which a CO2-acidified brine was injected into a fracture in the Dupe

55 omography before and after exposure to CO(2)-acidified brine, allowing mineral phase and voidspace di

56 We studied two CO2-acidified brines having the same pH (3.3) and comparable

57 ed intradermally to nape or cheek skin, (ii) acidified buffer elevated intracellular calcium levels i

58 In cells acidified by 5 minutes of exposure to 20 mM ammonium chl

59 croglia also degrade fAbeta if lysosomes are acidified by an ammonia pulse-wash or by treatment with

60 man melanoma xenografts can be significantly acidified by induction of hyperglycemia combined with ad

61 a persistent ozonide in airway-lining fluids acidified by preexisting pathologies or inhaled particul

62 The intestinal cytoplasm is acidified by proton influx from the lumen during defecat

63 usly measured while cells were progressively acidified by superfusion with a bicarbonate-buffered sol

64 u370 abstracts the C2 pro-R proton, which is acidified by the polarization of the thiolester carbonyl

65 ytic vesicles containing these complexes are acidified, causing the heptamer to transform into a tran

66 creased pH(out) stops the outward current of acidified cells.

67 utyl-1-methylxanthine alkalinized NL ASL but acidified CF ASL; and (iii).

68 in TEs increased significantly following an acidified chlorite treatment.

69 agents used to alter organelle pH affect all acidified compartments and are poorly reversible.

70 rsible effect of M2 on the pH of a subset of acidified compartments in the cell.

71 ression of all IFITMs expanded vesicular and acidified compartments within cells, there were marked p

72 ascidians and 29% sponges after 100 days in acidified conditions (pH 7.7).

73 Long-term exposure to acidified conditions predicted for the year 2100 and bey

74 ariability found among samples maintained in acidified conditions relative to controls, suggests a po

75 communities maintained in or transplanted to acidified conditions, and altered community structure in

76 cyanobacterium Trichodesmium decreased under acidified conditions, notwithstanding a beneficial effec

77 berrant shapes being observed only under the acidified conditions.

78 increase in the abundance of Padina spp. in acidified conditions.

79 y undergo maturation and become increasingly acidified, consistent with the formation of an autolysos

80 he charging of cytochrome c ions formed from acidified denaturing solutions generally increases with

81 dissolution of calcite particles by flow of acidified desalinated water through a bed packed with mi

82 y flow of micron-size calcite particles with acidified desalinated water.

83 In acidified dough the pattern of volatile metabolites allo

84 were investigated and compared to chemically acidified dough.

85 an; rescue can also be achieved by providing acidified drinking water to sublytic homozygotes.

86 elevated summer temperatures in historically acidified ecosystems.

87 r structures that colocalize with markers of acidified endosomal compartments.

88 n binding between PA and its receptor in the acidified endosome environment.

89 esting RGS4 traffics through PM recycling or acidified endosome pathways.

90 transfer of Wg to DFz2 within the merged and acidified endosome to initiate Wg signaling.

91 of cellular entry requires trafficking to an acidified endosome, which promotes translocation across

92 serving as a route of export of folates from acidified endosomes and (ii) provide a functional role f

93 dendritic cells (pDCs) detect viruses in the acidified endosomes by means of Toll-like receptors (TLR

94 diphtheria toxin catalytic domain (DTA) from acidified endosomes into the cytoplasm of eukaryotic cel

95 is generally leads to virion inactivation in acidified endosomes or degradation in lysosomes.

96 facilitates egress of the viral genome from acidified endosomes, and the L2/DNA complex accumulates

97 lfate-resistant PA oligomer, which occurs in acidified endosomes, but did not prevent cell surface PA

98 oxin, which enters the cytosol directly from acidified endosomes, were screened for abnormalities in

99 LF x PA complexes are then trafficked to acidified endosomes, where PA forms heptameric pores in

100 gests hosts may need to adapt not only to an acidified environment, but also to changes in their Symb

101 increased in solid tumors in response to an acidified environment, the appearance of hypopigmented c

102 The blueberries were soaked in acidified ethanol, filtered, and the filtrate was cleane

103 one concentration (%), time of extraction in acidified ethanolic solution (min) and ethanol concentra

104 ate was extracted from M. xanthus cells with acidified ethyl acetate and sequentially purified by sol

105 Samples were extracted with acidified ethyl acetate, MgSO4 and CH3COONa and cleaned

106 resorb mineralized tissue and cannot form an acidified, extracellular resorption compartment.

107 eactions in fractured basalts exposed to CO2-acidified fluids.

108 E. ictaluri-containing vacuoles (ECV) became acidified following ingestion by head kidney-derived mac

109 This compartment must be acidified for Salmonella to survive within macrophages,

110 Decades of acid rain have acidified forest soils and freshwaters throughout montan

111 ort function gradually decreasing when pH is acidified from 8.0 to 5.5.

112 The root cap apoplast acidified from pH 5.5 to 4.5 within 2 min of gravistimul

113 eystone organism in a more nutrient-limited, acidified future ocean.

114 Specimens were demineralized using acidified gel (pH = 4.5) for 5 wk and scanned every week

115 s were grown to the mid-logarithmic phase on acidified glucose minimal medium, conditions that induce

116 nant protein and electron cryo-microscopy of acidified hantavirus allows us to propose a model for en

117 Acidified Hepes (N-2-hydroxyethylpiperazine-N'-2- ethane

118 of the bacteria-containing phagosome into an acidified, hydrolytically active compartment.

119 n 5days and then approximately pH 8.5) to be acidified in PLGA MS for 9weeks, unlike CM2-free PLGA MS

120 ic pre-insertion form of PA (the prepore) is acidified in solution, it rapidly loses the ability to i

121 mers that undergo conformational change when acidified in the endosome.

122 into the intestinal lumen and are lacking in acidified intestinal V-ATPase-containing compartments.

123 ore appears to be pH dependent, requiring an acidified intracellular compartment.

124 In both cell types, virions localized to acidified intracellular organelles.

125 reasing acidosis temperature to 37 degrees C acidified intracellular pH and depressed synaptic respon

126 either genetic or pharmaceutical approaches acidified intracellular pH and reduced cell growth.

127 ate aCSF, pH 6.70 for 30 min at 32 degrees C acidified intracellular pH from 7.19+/-0.13 to 6.43+/-0.

128 (aCSF), pH 6.70 for 30 min at 32 degrees C, acidified intracellular pH from 7.31+/-0.12 to 6.53+/-0.

129 ologic agent of Q fever, inhabits a spacious acidified intracellular vacuole which is prone to fusion

130 or 9 (TLR9) is activated by DNA presented in acidified, intracellular compartments.

131 Polyacetylenes were retained better in acidified juices and cold storage temperatures (4 degree

132 pace between the intestine and the muscle is acidified just prior to muscle contraction and that the

133 -524) is sufficient to pilot the effector to acidified LAMP1-positive lysosomal compartments, where W

134 Despite localization to acidified late phagosomes, viable G. bethesdensis cells

135 ) cortical neurons, the GA is severely under-acidified, leading to osmotic swelling.

136 l pathogen that replicates exclusively in an acidified, lysosome-like vacuole.

137 and 2-(acetylamino)-2-methyl propanol (8) in acidified MeCN solution.

138 e CiaRH, ComDE, or VicRK grew more slowly in acidified media and were more sensitive to killing at le

139 of the wild-type strain grown in neutral and acidified media under conditions favoring induction of g

140 mutants showed a reduced ability to grow in acidified medium.

141 The epsilon in acidified MeOH and buffer pH 1 ranged between ~16,000-30

142 hilized fruit samples were extracted with an acidified MeOH mixture assisted by ultrasound.

143 ic-lipophilic balanced resin and eluted with acidified methanol (0.1% formic acid), resulting in anal

144 and to evaluate their spectral behaviors in acidified methanol (MeOH) and buffers pH 1-9.

145 Major anthocyanins were extracted with acidified methanol and characterised in powdered berry e

146 udes cell lysis, protein precipitation using acidified methanol and HPLC analysis of the lysate.

147 Compared with methanol solvent, using acidified methanol led to increased extraction yield by

148 om minced muscle samples involved the use of acidified methanol, ultrasound treatment and centrifugat

149 An acidified methanol-water mixture was used as an effectiv

150 The method is based on extraction with an acidified methanol-water mixture.

151 s commonly used for phenols, extraction with acidified methanol-water was chosen as the best to quant

152 casseliflavus and 20 E. gallinarum isolates) acidified MGP, 41 of 46 (89%) were LM and ARA positive,

153 y with its potent inhibitor HOE 642 not only acidified microglia, abolished the BK-triggered dynamic

154 Sample preparation improvements included acidified, microwave-accelerated, PNGase F N-glycan rele

155 ubjects were randomly assigned to receive an acidified milk drink containing >/=10(9) colony-forming

156 were important during exponential growth in acidified minimal medium containing glucose but were unn

157 duced tandem fluorophore protein reporter of acidified mitochondria reveals that acidified axonal mit

158 Selective oxidation of a-PhobPH in an acidified mixture of a-PhobPH and s-PhobPH is an efficie

159 feature of these key species in the reduced acidified molybdate solutions and to observe the templat

160 ncentrations increase considerably in gypsum-acidified must, although they fell markedly after fermen

161 nced precipitation was, however, observed in acidified NaHCO(3) solutions (pH 5, DIC approximately 25

162 ollowing topical application of the NO donor-acidified nitrite (NO2(-)), has set the paradigm of NO b

163 e nitrogen species produced biochemically as acidified nitrite and by bone marrow-derived macrophages

164 and a treatment arm that received 3 doses of acidified nitrite applied topically for 12 weeks with an

165 We report that acidified nitrite caused a 3-log-increased kill of C. je

166 nitrosylation upon exposure of Salmonella to acidified nitrite, a signal encountered by this enteropa

167 culosis uvrB result in severe sensitivity to acidified nitrite, a source of nitric oxide (6).

168 In contrast acidified nitrite, releasing equal quantities of NO (mea

169 s that are unable to grow in the presence of acidified nitrite, the cadC gene product was identified

170 Two acidified nitrite-inducible genes of Salmonella enterica

171 ll is substantially increased by exposure to acidified nitrite.

172 mine cadaverine and increased sensitivity to acidified nitrite.

173 itro and abrogated protection of Mtb against acidified nitrite.

174 ransposon mutants for hypersusceptibility to acidified nitrite.

175 gest that the potent inflammation induced by acidified NO2(-) is secondary to the release of addition

176 daptive capacity of species to respond to an acidified ocean, and, as a result, predictions regarding

177 S stained intensely for the vATPase and were acidified, only 20 to 30% of phagosomes containing live

178 ke of anthropogenic carbon dioxide (CO2) has acidified open-ocean surface waters by 0.1 pH units sinc

179 ine because global pH perturbants affect all acidified organelles in the cell and also have numerous

180 activity affects the pH of only a subset of acidified organelles, and its activity can be rapidly re

181 inetics in Cd-Zn cocontaminated alkaline and acidified paddy soils, under various flooding periods an

182 intracellular pathogen that replicates in an acidified parasitophorous vacuole derived from host lyso

183 n, the pathogen replicates exclusively in an acidified (pH 4.5 to 5) phagolysosome-like parasitophoro

184 these markers and thus were not appreciably acidified (pH 6.7).

185 gote stage of the parasite that lives within acidified phagolysomal vesicles of mammalian macrophages

186 e intracellular bacterium that resides in an acidified phagolysosome and has a remarkable ability to

187 Intracellularly, the organism prospers in an acidified, phagolysosome-like vacuole.

188 e normal process of phagosomes maturing into acidified phagolysosomes.

189 7-positive stage, but do not mature to fully acidified phagolysosomes.

190 bility to acid pH and reduced survival in an acidified phagosomal vacuole.

191 How the bacterium resists the low pH of the acidified phagosome is incompletely understood.

192 stigating the survival of mycobacteria in an acidified phagosome-like compartment.

193 iplasmic protease MarP for Mtb to survive in acidified phagosomes and establish and maintain infectio

194 Activated macrophages produce NO, which in acidified phagosomes is converted to NO(2).

195 ce are metabolically inactive, reside within acidified phagosomes that have fused with Texas red dext

196 ence are metabolically active, reside in non-acidified phagosomes that have not fused with Texas red

197 esistance, and intracellular survival within acidified phagosomes.

198 I-LC-MS/MS when the inactivated samples were acidified prior to analysis, indicating a requirement fo

199 liver, more mature populations of endosomes acidified progressively more slowly, but both toxins and

200 SA300 clone, the USA300-containing phagosome acidified rapidly and acquired the late endosome and lys

201 The protein storage vacuole (PSV) becomes acidified rapidly when aleurone cells are treated with g

202 ton gradient (DeltapH, where the endosome is acidified relative to the cytosol) is a potent driving f

203 ires osteoclasts to generate and maintain an acidified resorption compartment between the apical memb

204 r polarization and formation of an isolated, acidified resorptive microenvironment.

205 tected hBD-1 peptide in unstimulated, whole, acidified saliva from normal volunteers.

206 ve flow-through CO2 equilibration between an acidified sample and an indicator solution with a fast r

207 ve flow-through CO2 equilibration between an acidified sample and an indicator solution with a respon

208 ydrides were generated in the reaction of an acidified sample with NaBH4 after pre-reduction with KI-

209 Acidified samples were spiked and equilibrated with an e

210 reviewed experimental data on the effects of acidified seawater on calcifying species growth, reprodu

211 s of PNH erythrocytes in a modified extended acidified serum assay, and also prevents C3 fragment dep

212 sis), and, usually, a positive result on the acidified serum lysis test.

213 ysmal nocturnal hemoglobinuria in either the acidified serum or "sugar water" tests.

214 opment, allowing serpulids to do best at the acidified site by the end of the experiment, although ea

215 We show that succession at the acidified site was initially delayed (less community cha

216 pH(i) recovery was significantly greater in acidified slc4a10-transfected cells than in control cell

217 Nitrite addition to the acidified sludge at a concentration of 20 mg NO2(-)-N/L

218 e survival of most strains exposed to either acidified sodium nitrite (ASN) or hydrogen peroxide (H(2

219 nical Mycobacterium tuberculosis isolates to acidified sodium nitrite (ASN) were compared.

220 ant in vitro than other clinical isolates to acidified sodium nitrite (ASN), a generator of reactive

221 d to grow at higher rates in the presence of acidified sodium nitrite (ASN), a model system used to g

222 utathione or the nitric oxide (NO)-generator acidified sodium nitrite (NaNO(2)) during aerobic growth

223 ant to both hydrogen peroxide (H(2)O(2)) and acidified sodium nitrite than were the other strains tes

224 tro and was highly susceptible to killing by acidified sodium nitrite.

225 othesis that calcium limits forest growth in acidified soils.

226 77-83% moisture content) were conditioned in acidified solution at 5, 15 and 25 degrees C, absence of

227 t of carbonate mineral reactivity with CO(2)-acidified solution is voidspace generation through physi

228 Microinfusion of acidified solutions into the rhythmically active pre-Bot

229 In weakly acidified solutions, 1 exhibited strong toxicity to canc

230 hm as small as 3.7% achieved in desalted and acidified solutions.

231 nvironmental problem, but efforts to restore acidified streams and biota have had limited success.

232 The secondary production of culturally acidified streams is low, with a few species of generali

233 ta vacuoles were alkalinized and the cytosol acidified, suggestive of impaired V-ATPase proton transp

234 teine, albumin, and hemoglobin are stable in acidified sulfanilamide as determined by the tri-iodide

235 This claim is based on the beliefs that (i) acidified sulfanilamide pretreatment, required to remove

236 ations were only enhanced in the presence of acidified sulfate aerosol, consistent with prior work.

237 Additionally, we show reactive uptake on the acidified sulfate aerosols supports a previously unrepor

238 ich form during the BVOC oxidation, into the acidified sulfate particles is shown to explain the latt

239 low-NO(x) SOA is enhanced in the presence of acidified sulfate seed aerosol (mass yield 28.6%) over t

240 facility in the presence of nonacidified and acidified sulfate seed aerosol.

241 otons (coreleased with neurotransmitter from acidified synaptic vesicles).

242 s wave EPR spectra of RPE cells and TREPR of acidified synthetic melanin suggest that increased melan

243 Vesicles rapidly acidified (t(1/2) approximately 10 ms) in response to HC

244 Following transport to the acidified TGN/endosomal compartments, furin cleaves the

245 did not occur, and the cytoplasm became more acidified than in the presence of Na(+).

246 CS exposure acidified the airspaces and induced localization of the

247 ubating the cells with HCO(3)(-) or butyrate acidified the cytosol and increased the selectivity of S

248 Inhibition of extramitochondrial CA activity acidified the matrix (as determined by fluorescence meas

249 ion of vacuolar-type H(+)-ATPase components, acidified the pericellular milieu, and maintained extrac

250 Illumination with amber light acidified the surrounding interstitium and led to activa

251 They acidified the yeast cytosol and caused pH-sensitive grow

252 When the interior of the proteoliposomes was acidified, the addition of aminoglycosides to the extern

253 l growth, all of these Lactobacillus species acidified their growth medium at rates on the order of 1

254 L. vaginalis, L. crispatus, and L. jensenii-acidified their growth medium to an asymptotic pH (3.2 t

255 /endosomal network and vacuolar membrane and acidified these compartments as part of a hybrid V-ATPas

256 mes, within a C. neoformans-containing cell, acidified to a lesser extent and failed to recruit CD63

257 In the first hour, DC phagosomes acidified to a pH that was, on average, half a point hig

258 Sample water is first acidified to convert all DIC to carbon dioxide (CO2).

259 ionein(MT)-bound and non-MT-bound Cd(II) was acidified to displace the Cd(II) from MT.

260 total dissolved iron analysis, samples were acidified to pH 2.0 in the presence of 30 muM DHN and le

261 olerance was assessed in 48 pups fed formula acidified to pH 3 with either hydrochloric acid or citri

262 intained around -120 mV, and the apoplast is acidified to pH 3.

263 In turn, these salts can be acidified to produce the functionalized aryl acids or tr

264 mobilization of metal contaminants by brine acidified upon contact with CO2 during geologic carbon s

265 PC-PLC activation occurs in the acidified vacuolar environment.

266 ate intracellular bacteria that occupy a non-acidified vacuole (the inclusion) during their entire de

267 ns remain regarding how bacteria survive the acidified vacuole and how acidification affects bacteria

268 of macrophages, where Brucella resides in an acidified vacuole at a pH of 4-4.5 during the early phas

269 ts growth medium in vitro, and resided in an acidified vacuole within macrophages.

270 m was not impaired following fusion with the acidified vacuole.

271 virulence mechanisms differentially rely on acidified vacuoles and that the loss of both vacuolar (V

272 fection, PC-PLC is activated specifically in acidified vacuoles.

273 rowth rate of M. tuberculosis was reduced in acidified vacuoles.

274 lar proton pump, blocked MDP accumulation in acidified vesicles and cytokine responses, suggesting th

275 c machinery to discriminate fully loaded and acidified vesicles from vesicles undergoing neurotransmi

276 MDP is internalized into acidified vesicles in macrophages.

277 ation, labeled MDP was rapidly released from acidified vesicles into the cytosol, a process that requ

278 et cells triggers toxin internalization into acidified vesicles, whereupon cryptic segments from with

279 blocking the fusion of early endosomes with acidified vesicles.

280 ons from the cell surface to the appropriate acidified vesicular compartment where fusion occurs.

281 The desolvated solutions were dispersed in acidified water (pH 3) immediately after desolvation.

282 A gradient method was developed using acidified water and acetonitrile combined with high colu

283 Extractions with acidified water and ultrasound were not effective to rec

284 ects of the extraction methods and solvents (acidified water pH 2.0, ethanol+water 50% v/v and ethano

285 The haloacetic acids are extracted from acidified water through a microscale liquid-liquid extra

286 ite electrode readily produces hydrogen from acidified water when functionalized with the modified cl

287 terials and with a diffusion-limited rate in acidified water, is efficient as well as oxygen tolerant

288 bly linked to a pyrite electrode immersed in acidified water.

289 cumvented if rats are maintained on neomycin/acidified water.

290 5) degradation over 2 weeks when prepared in acidified water.

291 sistent spatial mosaic in the penetration of acidified waters into ecologically-important nearshore h

292 The cytoplasm is acidified when V-ATPase is inhibited; thus we conducted

293 extraction with primary secondary amine and acidified with 0.1% formic acid.

294 In the assay, cell samples are directly acidified with 4 M H(2)SO(4) in sealed reaction vials.

295 modified QuEChERS technique in acetonitrile acidified with acetic acid (1%, v/v) and citrate-buffere

296 extraction was performed using acetonitrile acidified with formic acid (1%, v/v).

297 Samples were dissolved in water and acidified with HNO3.

298 Cells were acidified with NH(4)Cl (25 mM, 1 min) and pH(i) recovery

299 Winemaking of musts acidified with up to 3g/L of gypsum (CaSO4 2H2O) and tar

300 Inclusion of MTGase into acidified yogurt drinks reduces the serum separation wit