ライフサイエンスコーパス: orthophosphate

1 64 h for 90Y-citrate and Te = 255 h for 32P-orthophosphate).

2 /- 0.03 mg-P.L(-1) (0.01 +/- 0.02 mg-P.L(-1) orthophosphate).

3 following incubation of cells with [(32)P(i)]orthophosphate.

4 h (15) N-labelled algal necromass and (33) P orthophosphate.

5 from MDA-486 cells labeled in vivo with [32P]orthophosphate.

6 sphate, releasing two molecules of inorganic orthophosphate.

7 from in-line geometry with respect to bound orthophosphate.

8 e and water (or OH-) are in equilibrium with orthophosphate.

9 pyruvate, adenosine triphosphate (ATP), and orthophosphate.

10 was studied by metabolic labeling with (32)P-orthophosphate.

11 eady state exceeded by 3-fold that of [(32)P]orthophosphate.

12 Mv1Lu cells) metabolically labeled with [32P]orthophosphate.

13 e cells were metabolically labeled with [32P]orthophosphate.

14 GA and increased resistance to the inhibitor orthophosphate.

15 ractable phosphorus, but only if measured as orthophosphate.

16 and a decreased sensitivity to the inhibitor orthophosphate.

17 n45.6 and connexin56, were labeled with [32P]orthophosphate.

18 bolically labeled with 32P-labeled inorganic orthophosphate.

19 vivo labeling of PS120/NHE3V cells with [32P]orthophosphate.

20 hydrolyzed concomitantly to produce ADP and orthophosphate.

21 residue(s) when excised shoots were fed [32P]orthophosphate.

22 y in vivo labelling of these cells with 32 P-orthophosphate.

23 by a nucleophilic water molecule to release orthophosphate.

24 ons than the corresponding condition without orthophosphate.

25 o generate flavonoid monophosphates, AMP and orthophosphate.

26 o other conditions at pH 6.5 and pH 9.0 with orthophosphate.

27 the greatest amount of NaOH-EDTA extractable orthophosphate.

28 owed soil contained lowest concentrations of orthophosphate.

29 diacylglycerol (DAG), dihydroxyacetone, and orthophosphate.

30 iphosphates to nucleoside monophosphates and orthophosphates.

31 )), which are more soluble and reactive than orthophosphates.

32 lts in protein precipitation, the effects of orthophosphate (0-64 mM) addition to sodium caseinate so

33 mg/L as P) < hexametaphosphate (0.1 mg/L) < orthophosphate (0.3 mg/L).

34 ella bronchiseptica GmhB bound to Mg(2+) and orthophosphate (1.7 A resolution).

35 A resolution), in a complex with Mg(2+) and orthophosphate (1.8 A resolution), and in a complex with

36 in another four prawn samples that contained orthophosphate (10225 +/- 1102 ug/g), as well.

37 hromatography revealed that it was all (32)P-orthophosphate ((32)P(i)).

38 ne-seeking radiopharmaceuticals, such as 32P-orthophosphate, 89Sr-chloride, 186Re-1,1 hydroxyethylide

39 In response, Newark initiated orthophosphate addition and provided faucet-mounted poin

40 In all experiments with orthophosphate addition of at least 1 mg/L as P, peaking

41 sed the year-long impacts of full-scale DWDS orthophosphate addition on both the microbial ecology an

42 Orthophosphate addition reduced bioavailability of coppe

43 Orthophosphate addition, however, represses mitotic PHO5

44 total bacterial density were observed after orthophosphate addition, likely driven by a 2 log 10 inc

45 significant compositional changes after the orthophosphate addition.

46 sence of different phosphate anions, such as orthophosphate, adenosine triphosphate, and tripolyphosp

47 Orthophosphate and 3'-phosphates were also detected in t

48 he similarity in pain relief afforded by 32P-orthophosphate and 89Sr-chloride, this hypothesis is exa

49 .0020 cGy/h/kBq and 0.0026 cGy/h/kBq for 32P-orthophosphate and 90Y-citrate, respectively.

50 vage of phosphonoacetaldehyde (Pald) to form orthophosphate and acetaldehyde.

51 nophosphate, while ADP is hydrolyzed to form orthophosphate and AMP.

52 anic polyphosphate (polyP) is the polymer of orthophosphate and can be found in all living organisms.

53 vivo by pulse-labeling HeLa cells with [32P]orthophosphate and chasing using three different techniq

54 ADP is attacked by water with liberation of orthophosphate and formation of AMP.

55 At neutral pH, products of the reaction (orthophosphate and fructose 6-phosphate) bind to the act

56 used to determine the binding force between orthophosphate and iron (oxy)hydroxide that was coated o

57 in the raw activated sludge was dominated by orthophosphate and long-chain polyphosphates, whereas in

58 lar techniques and supplied them with (33) P-orthophosphate and O. vulgatum sporophytes with (14) CO2

59 C phosphorylation sites incorporated [(33)P]-orthophosphate and showed a progressive decrease with no

60 proteins, RASM cells were labeled with [32P]orthophosphate and stimulated with 100 nmol/L Ang II for

61 tor, YT cells were radiolabeled with [(32)P]-orthophosphate and stimulated with Interleukin-2.

62 t 2B7 incorporated immunoprecipitable [(33)P]orthophosphate and that 2B7His, previously expressed in

63 egates were governed by the concentration of orthophosphate and the aggregates consisted of all casei

64 Orthophosphate and the oxoanion analogues orthovanadate,

65 ic degradation of long-chain phosphates into orthophosphate and trimetaphosphate whereas heating the

66 The competition between orthophosphate and water-extractable organic matter (WEO

67 Inhibitor blends (Zn+orthophosphate and Zn+NOM+orthophosphate) had stronger i

68 x formed as a result of the reaction between orthophosphates and molybdates ions where ascorbic acid

69 ntly validated through the quantification of orthophosphates and total dissolved phosphorus in pollut

70 ) by Lp(a)-associated enzymes helps generate orthophosphate, and apolipoprotein(a) blocks plasmin-ind

71 -1beta (10 U/ml, 4 h) were labeled with [32P]orthophosphate, and E-selectin was immunoprecipitated us

72 te, hydrocerussite, chloropyromorphite, lead orthophosphate, and lead oxide solids; however, in the p

73 the other hand, AMP, in the presence of GDP, orthophosphate, and Mg(2+), adopts the binding mode of a

74 itivity to its negative allosteric effector, orthophosphate, and more stable interactions between lar

75 identified intracellular P as polyphosphate, orthophosphate, and pyrophosphate.

76 rophosphate, and phosphoenolpyruvate to ATP, orthophosphate, and pyruvate and provides diverse functi

77 and water to catalyze the formation of AMP, orthophosphate, and selenophosphate.

78 tosomes were metabolically labeled with [32P]orthophosphate, and solubilized homogenates were subject

79 the significant clinical experience with 32P-orthophosphate, and the similarity in pain relief afford

80 reveals new insight into the consequences of orthophosphate application on the DWDS microbiome and hi

81 udy, we investigated the mechanistic role of orthophosphate as a corrosion inhibitor in controlling l

82 termine the overall lead exposure when using orthophosphate as a corrosion inhibitor.

83 tic phosphorylation reactions have relied on orthophosphate as the source of phosphorus.

84 very low soil solution concentration of free orthophosphate, as they contain high concentrations of s

85 H from 6.5 to 9.0 and the addition of 6 mg/L orthophosphate at pH 6.5 and 9.0 slowed down the copper

86 emoval of two terminal phosphate moieties as orthophosphate (Bacillus subtilis) or pyrophosphate (Esc

87 Five or more orthophosphates bound together by high-energy phosphoanh

88 high concentrations of Ca(2+) and inorganic orthophosphate, but pH and/or other ligands for Ca(2+) ,

89 itates resulted in gradual adsorption of the orthophosphate, causing re-dispersion of the casein-iron

90 d of a hitherto unknown sodalite-type silver orthophosphate cluster (SOC) {(Ag(3) PO(4) )(8) }, remin

91 phosphates, supports an in vivo role for the orthophosphate complex of Mn(2+) in resistance to oxidat

92 d AGP activity in the presence of a range of orthophosphate concentrations in vitro.

93 ased from sediments, leading to bottom water orthophosphate concentrations increasing by a factor of

94 es isolated from induced plants had a higher orthophosphate content than granules from noninduced con

95 This study identifies key factors (e.g., orthophosphate, copper resistance, and anode materials)

96 amine the effects of copper dose (0-2 mg/L), orthophosphate corrosion control agent, and water heater

97 Orthophosphate corrosion control was used in both system

98 prosolvency problems through the addition of orthophosphate corrosion inhibitors.

99 ing of the other reaction product (inorganic orthophosphate) could not be detected.

100 t run backward synthesizing ATP from ADP and orthophosphate; (d) that its mechanism is a ping-pong on

101 ng of wild-type and mutant B cells with [32P]orthophosphate demonstrated that each of the RFX subunit

102 aortic endothelial cells labeled with [(32)P]orthophosphate demonstrated that only phosphoserine was

103 pyrophosphatase 1, followed by colorimetric orthophosphate detection.

104 avage of triphosphate into pyrophosphate and orthophosphate did not occur, indicating that triphospha

105 Increased total organic P and orthophosphate diesters by P NMR and accumulated inosito

106 s further supported the reduction in organic orthophosphate diesters on day 30.

107 e surface soils showed higher proportions of orthophosphate diesters under paddy than under non-paddy

108 enesis, as exemplified by cytosolic PYRUVATE ORTHOPHOSPHATE DIKINASE (cyPPDK).

109 emperatures with altered amounts of pyruvate orthophosphate dikinase (PPDK) and Rubisco or altered pr

110 mbined with the cytosolic/plastidic pyruvate orthophosphate dikinase (PPDK) catalyze two key steps du

111 horibosyl transferase (APRTase) and pyruvate orthophosphate dikinase (PPDK) convert adenine to ATP fo

112 The enzyme pyruvate,orthophosphate dikinase (PPDK) interconverts pyruvate an

113 Pyruvate orthophosphate dikinase (PPDK) is a critical enzyme for

114 Pyruvate orthophosphate dikinase (PPDK) is a key enzyme in C(4) p

115 Pyruvate, orthophosphate dikinase (PPDK) is a ubiquitous, low-abun

116 RT-DD also detected mRNA for pyruvate, orthophosphate dikinase (PPDK) which has already been sh

117 included the two known isoforms of pyruvate orthophosphate dikinase (PPDK), large and small subunits

118 sphoribosyl transferase (APRT), and pyruvate orthophosphate dikinase (PPDK), respectively.

119 bidopsis, and that the second uses pyruvate, orthophosphate dikinase (PPDK).

120 se in addition to the reduction of pyruvate, orthophosphate dikinase activity in o2 endosperm is comp

121 specific) and the genes that encode pyruvate orthophosphate dikinase and phosphoenolpyruvate carboxyl

122 sferase converts adenine to AMP and pyruvate orthophosphate dikinase converts AMP to ATP.

123 umulation of two isoforms of CA and pyruvate,orthophosphate dikinase in M cells.

124 g phosphoenolpyruvate carboxylase, pyruvate, orthophosphate dikinase, and the 2'-oxoglutarate/malate

125 Trends of delta(18)O values in released orthophosphate during each enzyme-catalyzed reaction in

126 ounts of calcium to maintain phosphate in an orthophosphate environment in the glass.

127 Both in vivo radiolabeling (using [(32)P]orthophosphate) followed by thin-layer or high-performan

128 Phosphorus, in its orthophosphate form (P(i)), is one of the most limiting

129 Increasing orthophosphate from 0.5 to 1.0 mg L(-1) (as PO4(3-)) acc

130 '-labeling of the adducts by transfer of 32P-orthophosphate from [gamma-32P]ATP mediated by polynucle

131 5'-end-dependent RNA degradation by removing orthophosphate from the 5'-diphosphorylated transcripts.

132 oups bind irrotationally to bone, displacing orthophosphate from the bone mineral matrix.

133 hosphatase and atypically releases inorganic orthophosphate from triphosphates instead of pyrophospha

134 Gallium orthophosphate (GaPO4) is an alternative piezoelectric m

135 e-dispersed soluble complexes of casein-iron-orthophosphate generated using this process could be use

136 delivered by meteorites, can be oxidized to orthophosphate, generating thiophosphate in the process.

137 lyphosphate (polyP) is an anionic polymer of orthophosphate groups linked by high energy bonds that t

138 hibitor blends (Zn+orthophosphate and Zn+NOM+orthophosphate) had stronger inhibitory effects compared

139 Addition of orthophosphate has been commonly employed to suppress le

140 Orthophosphate immobilized oxidized lead as insoluble hy

141 iosynthesis of monoselenophosphate, AMP, and orthophosphate in a 1:1:1 ratio from selenide and ATP.

142 is examined in this study using 32P- and 33P-orthophosphate in a mouse femur model.

143 monstrated increased incorporation of [32PO4]orthophosphate in drug-treated cells.

144 resulted in the production of only inorganic orthophosphate in the hydrochar.

145 rporation of 18O from H218O exclusively into orthophosphate in the overall selenide-dependent reactio

146 equivalent labeling of the protein with [32P]orthophosphate in the presence and absence of cyclohexim

147 endent inhibition of immunodetectable [(33)P]orthophosphate in UGTs and protein kinase Cepsilon (PKCe

148 replication by metabolic labeling with [32P]orthophosphate in vivo and obtained direct evidence that

149 P is converted quantitatively to AMP and two orthophosphates in a very slow partial reaction.

150 ar UGT1A7 and UGT1A10 activities and of [33P]orthophosphate incorporation into immunoprecipitable pro

151 n of protein kinase A (PKA) increased [(32)P]orthophosphate incorporation into perilipin 5 by 2-fold,

152 Use of [(32)P]orthophosphate incorporation, pervanadate treatment, and

153 mer-requested sampling after the addition of orthophosphate indicated below detection levels for 59%

154 1 followed by metabolic labeling with [(32)P]orthophosphate indicated that p42(mapk/erk2) phosphoryla

155 Metabolic labeling studies using [32P]orthophosphate indicated that the poor prenylation of th

156 ctrometry analyses confirmed that the pH and orthophosphate inhibited copper corrosion with different

157 In fact, orthophosphate, inorganic tripolyphosphate (3polyP), ade

158 f colloidal structures involving casein-iron-orthophosphate interactions.

159 The incorporation of [32P]orthophosphate into immunoprecipitated TTF-1 protein als

160 inase C, also enhanced incorporation of [32P]orthophosphate into TTF-1 protein; however, the DNA bind

161 phous calcium phosphate (ACP) rich in acidic orthophosphate ions and water molecules.

162 Measuring orthophosphate is an important tool in biochemical analy

163 ymatic hydrolysis of these esters to produce orthophosphate is often a required reaction preceding ph

164 Free orthophosphate is the form of P taken up by plants, but

165 cies are long-term labeled in vivo with [32P]orthophosphate, isolated in a highly selective way, enzy

166 tes and eukaryotes synthesize long chains of orthophosphate, known as polyphosphate (polyP), which fo

167 By immunoprecipitation carried out on [(32)P]orthophosphate-labeled AtT-20 pituitary cells stably exp

168 First, [(32)P]orthophosphate-labeled cells (Sf9, 3T3-L1 fibroblasts, a

169 Separating tryptic peptides from [(32)P]orthophosphate-labeled cells and analyzing the phosphope

170 Furthermore, in [(32)P]orthophosphate-labeled cells, pantophysin was phosphoryl

171 [32P]Orthophosphate-labeled dUTPase was purified from HeLa ce

172 Phenol-chloroform extraction of [(32)P]orthophosphate-labeled Escherichia coli cells followed b

173 Exposure of [(32)P]orthophosphate-labeled human pulmonary artery endothelia

174 increased in response to TNFalpha in [(32)P]orthophosphate-labeled macrophages, although the level o

175 tion and ODC immunoprecipitation from [(32)P]orthophosphate-labeled NHEK lysates showed that a phosph

176 as confirmed by showing a 2-fold increase in orthophosphate-labeled Sp1 with EGF and okadaic acid.

177 or protein was markedly stimulated when [32P]orthophosphate-labeled Swiss 3T3 cells or CHO-mBR1 cells

178 However, immunoprecipitation of [32P] orthophosphate-labeled UBF from hypertrophying neonatal

179 Immunoprecipitation of [32P]orthophosphate-labeled UBF from hypertrophying, neonatal

180 Orthophosphate labeling and immunoprecipitation of an ep

181 irmed to be phosphorylated in vivo by [(32)P]orthophosphate labeling and peptide mapping.

182 Additionally, orthophosphate labeling coupled with phosphoamino acid a

183 Phosphatase treatment and orthophosphate labeling demonstrated that the species wi

184 In vivo [32P]orthophosphate labeling experiments demonstrated that PP

185 otransfected IRS-1 as demonstrated by [(32)P]orthophosphate labeling experiments.

186 In vivo [32P]orthophosphate labeling indicated that the rescue of the

187 Metabolic [(32)P]orthophosphate labeling of human ARNT-transfected COS-1

188 1) Based on [(32)P]orthophosphate labeling of protein-bound nucleotide, Rab

189 mass spectrometry, mutagenesis, and [(32)P] orthophosphate labeling to identify that all five hydrox

190 Using orthophosphate labeling we showed a decrease in phosphor

191 Immunoprecipitation studies with [32P]-orthophosphate-labelled cells demonstrated that IncG is

192 radioimmunoprecipitation of lysates of [32P]-orthophosphate-labelled infected HeLa cells with anti-In

193 osphorylation of hERG was measured by [(32)P]orthophosphate labelling of immunoprecipitated protein w

194 n intact neutrophils was confirmed by [(32)P]orthophosphate loading, followed by fMLP stimulation in

195 Using a [32P]orthophosphate metabolic labeling procedure to study HDV

196 consists of an aqueous suspension of silver orthophosphate microparticles under UV illumination, in

197 Polyphosphate (polyP), a polymer of orthophosphate moieties released from the dense granules

198 s research confirmed that nonadherent Pb(II)-orthophosphate nanoparticles were an important form of P

199 The minimum doses of orthophosphate necessary to achieve acceptable cuprosolv

200 The effects of orthophosphate, nucleotide analogues, ADP, and covalent

201 After intravenous administration of 32P-orthophosphate or 90Y-citrate in Swiss Webster mice, DNA

202 ubstrate binding was not inhibited by either orthophosphate or glycerol 3-phosphate, indicating that

203 lowing metabolic labeling of cells with [32P]orthophosphate or in vitro in phosphorylation assays wit

204 tory effects compared to each inhibitor (Zn, orthophosphate or NOM) alone, whereas Zn+NOM showed a le

205 (31)P NMR showed comparable inorganic orthophosphate (ortho-P, 53-60% of total P) and organoph

206 sensing protocol allows the determination of orthophosphates over the range from 0.5 to 20 mug L(-1)

207 leaf phosphoenolpyruvate carboxylase [PEPC; orthophosphate:oxaloacetate carboxy-lyase (phosphorylati

208 , and phosphoenolpyruvate carboxylase [PEPC; orthophosphate:oxaloacetate carboxy-lyase (phosphorylati

209 relationships between five leaf P fractions (orthophosphate P, P(i); lipid P, P(L); nucleic acid P, P

210 ur assay, malachite green is used to measure orthophosphate (P(i)) concentrations after degradation b

211 ly TbIP(3)R disclosed that luminal inorganic orthophosphate (P(i)) or pyrophosphate (PP(i)), and neut

212 erichia coli detects environmental inorganic orthophosphate (P(i)) to regulate genes of the phosphate

213 nversion of adenosine 5'-triphosphate (ATP), orthophosphate (P(i)), and pyruvate with adenosine 5'-mo

214 In the presence of inorganic orthophosphate (P(i)), succinyl-CoA, and either GDP, ADP

215 d-enabled Donnan dialysis process to recover orthophosphate (P(V)) from alum-laden waste activated sl

216 minantly present in the water as fine Pb(II) orthophosphate particles.

217 dant complexes with small metabolites (e.g., orthophosphate, peptides), which exhibit narrow EPR sign

218 bacteria, P is acquired mainly as inorganic orthophosphate (Pi) and assimilated into adenosine triph

219 Pyruvate,orthophosphate (Pi) dikinase (PPDK) is best recognized a

220 olism and physiology, and to the pathways of orthophosphate (Pi) entry into the root, which increase

221 ethionine (AdoMet), pyrophosphate (PPi), and orthophosphate (Pi) from ATP and L-methionine.

222 Variation in the concentration of orthophosphate (Pi) in actively contracting, chemically

223 Inorganic orthophosphate (Pi) is an essential nutrient for plant g

224 the ability to convert phosphite (Phi) into orthophosphate (Pi) offers an alternative selectable mar

225 However, plants can only acquire inorganic orthophosphate (Pi), meaning global crop production is f

226 Mn(2+) coordinated by orthophosphate (Pi), metabolites, or peptides acts as a

227 A sensor for the determination of orthophosphate (PO(4)(3-)) concentration in water was de

228 oiting the enzymatic reaction of maltose and orthophosphate (PO(4)(3-)) in the presence of maltose ph

229 dominated blooms to nutrient amendments with orthophosphate (PO4) and inorganic and organic forms of

230 kinesis, we labeled eggs in vivo with [(32)P]orthophosphate, prepared cortices, and mapped LC20 phosp

231 ferred from UDP-N-acetyl[18O]muramate to the orthophosphate produced in the reaction.

232 However, we could document orthophosphate production from ATP catalyzed by the ATP-

233 Additionally, orthophosphate, pyrophosphate and phosphonates were also

234 haracterization of inorganic polyphosphates [orthophosphate, pyrophosphate, tripolyphosphate, trimeta

235 nts that suggest phosphate species including orthophosphates, pyrophosphates, and adenosine phosphate

236 nversion for various P(V) sources, including orthophosphates, pyrophosphoric acid, Na(3)P(3)O(9) and

237 rgy transfer, co-immunoprecipitation, [(32)P]orthophosphate radiolabeling, and measurement of lipolys

238 ynamics simulations further corroborate that orthophosphates readily cluster in aqueous solutions.

239 iron to sodium caseinate solution containing orthophosphate reduced the diffusible phosphorus content

240 Our findings provide insights to how orthophosphate reduces lead levels under drinking water

241 cess releases carbon to the solution whereas orthophosphate remains adsorbed on goethite.

242 t to rare earth sesquioxides (RE(2)O(3)) and orthophosphates (REPO(4)) using DFT computations with th

243 ions such as maintaining water chemistry and orthophosphate residuals and to ensure comparability to

244 osphates (polyP) consist of linear chains of orthophosphate residues, linked by high-energy phosphoan

245 coagulant inorganic polymer of linear-linked orthophosphate residues.

246 d day after injection of 90Y-citrate and 32P-orthophosphate, respectively.

247 dition of iron to caseins in the presence of orthophosphate results in the formation of colloidal str

248 ciated GAPDH by in vivo labeling with [(32)P]orthophosphate revealed the presence of multiple phospho

249 stressed HeLa cells, labeled in vivo by [32P]orthophosphate, revealed four major phosphopeptides A to

250 of epimastigotes labeled for 3 h with (32)P-orthophosphate showed a significant incorporation of the

251 est importance, in vivo labeling with [(32)P]orthophosphate showed that the tryptic phosphopeptide ma

252 egions, with a corresponding increase in the orthophosphate signal, as compared to unhydrolyzed extra

253 The addition of different concentrations of orthophosphate solution to the casein-iron precipitates

254 rea and choline chloride), utilizing various orthophosphate sources.

255 with alanine reduces incorporation of (32)P-orthophosphate substantially.

256 ermeabilized Jurkat T cells using a specific orthophosphate substrate.

257 In the presence of inorganic orthophosphate, succinyl-CoA, and an equimolar amount of

258 Calcium orthophosphates, such as hydroxyapatite (HAP), have been

259 of a novel assay procedure for quantitating orthophosphate that is extremely sensitive, reproducible

260 rganic polyphosphates are linear polymers of orthophosphate that modulate blood clotting and inflamma

261 pared with those obtained previously for 32P-orthophosphate, the radiochemical 117mSn(4+)DTPA yields

262 -01 and NIH 3T3 cells were labeled with [32P]orthophosphate to investigate COX phosphorylation in viv

263 lved in these responses, we used radioactive orthophosphate to pulse-label suspension-cultured cells

264 than 600 Da and the reduced binding force of orthophosphate to WEOM-adsorbed iron (oxy)hydroxide AFM

265 in polyphosphate metabolism and V-ATPase in orthophosphate transport were absent from CAP IB HKU-1.

266 e (Omegacalcite = 13), demonstrated that Zn, orthophosphate, tripolyphosphate, and hexametaphosphate

267 Darby bovine kidney cells, labeled with [32P]orthophosphate under normal culture conditions.

268 ine phosphorus excretion, and reduced [(33)P]orthophosphate uptake in rats.

269 complete digestion of the oligomer sample to orthophosphate using acid at high temperature and subseq

270 , all forms of phosphorus are converted into orthophosphates via sample digestion (heating and acidif

271 ssed in transfected cells labeled with [32P] orthophosphate was phosphorylated following the addition

272 th chloramine, with intermittent flow, or if orthophosphate was present.

273 The water pH 9.0 without orthophosphate was the most likely to induce localized c

274 Orthophosphate was very effective at reducing cuprosolve

275 pH buffer with strong complexing properties (orthophosphate) was employed in the background electroly

276 A model distribution system, dosed with orthophosphate, was used to evaluate the effect of corro

277 32P- and 33P-orthophosphate were administered intravenously, and GM-C

278 he nucleus incorporates radiolabel from [32P]orthophosphate whereas cytoplasmic VP22 does not.

279 totic activation is repressed by addition of orthophosphate, which significantly increases cellular p

280 f divalent cations, fructose 6-phosphate and orthophosphate, which together stabilize an R-state conf

281 This study explored the interactions of orthophosphate with casein-iron precipitates.

282 )] which is achieved by activation of [(32)P]orthophosphate with ethyl isocyanate followed by aminoly

283 The interactions of added orthophosphate with iron in the presence and absence of

284 W complexes with nitrogenous metabolites and orthophosphate, with negligible EPR signal from Mn(2+) o

285 vailable in Enceladus's ocean in the form of orthophosphates, with phosphorus concentrations at least

286 o sodium caseinate solution containing 32 mM orthophosphate without any protein precipitation.

287 titation of radiolabeled ATP and radioactive orthophosphate without the generation of large quantitie