ライフサイエンスコーパス: sodium phosphate

1 containing 20% (vol/vol) glycerol and 75 mM sodium phosphate.

2 itted by Enceladus that show the presence of sodium phosphates.

3 les were determined, protein, ash, chloride, sodium, phosphate.

4 ditives in products included lecithin (32%), sodium phosphate (13%), calcium phosphate (11%), modifie

5 nt solution conditions (14 uM Abeta42, 20 mM sodium phosphate, 200 uM EDTA, pH 6.8).

6 tment groups: saline solution, dexamethasone sodium phosphate, a nonparticulate steroid, and the part

7 r the elution of CRP, which contained 0.05 M sodium phosphate and 2.0 M NaCl (pH 4.5).

8 er gave higher purification performance than sodium phosphate and citrate-phosphate buffers in IMAC s

9 GII is intrinsically unfolded in 10 mM sodium phosphate and gives weak chromatosome protection,

10 loop of GI, termed GII-L, is stable in 10 mM sodium phosphate and is as effective as GI in chromatoso

11 Both sodium phosphate and magnesium citrate provided excellen

12 dominis plane (TAP) block with dexamethasone sodium phosphate and preperitoneal instillation of local

13 A cathartic (sodium phosphate) and an emetic (ipecac) were given to a

14 s stably folded at low ionic strength (10 mM sodium phosphate) and gives strong protection of chromat

15 ow concentrations of impurities (e.g., 20 mM sodium phosphate), and reduces or eliminates the catastr

16 g 10mmoll(-1) sodium tetraborate, 4mmoll(-1) sodium phosphate, and 25mmoll(-1) SDS.

17 high dose of intra-erythrocyte dexamethasone sodium phosphate, and 59 received placebo).

18 concentrations of SSC, SSPE, PBS, TRIS, MES, sodium phosphate, and potassium phosphate buffers, and f

19 ouble-stranded forms of the 28-mer in 0.01 M sodium phosphate at 25 degrees C, although long-chain (c

20 ty (P(50) = 28.2 mmHg, n(max) = 2.6 in 0.1 M sodium phosphate at pH 7.4) compared to those of Hb A (P

21 y after 120days of storage at 4 degrees C in sodium phosphate buffer (0.1M, pH 7.5), whereas the free

22 U of chondroitinase ABC in 50 microl of 1 mM sodium phosphate buffer (pH 7.0) at 37 degrees C for 6 h

23 heir corresponding DNA/DNA duplexes in 10 mM sodium phosphate buffer (pH 7.0) were determined from di

24 were incubated individually for 2 h in 10 mM sodium phosphate buffer (pH 7.2) containing 0.14 M NaCl,

25 In sodium phosphate buffer (pH 7.4) at 37 degrees C, an unu

26 monocytogenes, and Candida albicans in 10 mM sodium phosphate buffer (pH 7.4).

27 ended mixture consisting in acetonitrile and sodium phosphate buffer 10mmolL(-1) pH = 3.50 (30:70v/v)

28 dine side chains of the mutant rHbs in 0.1 M sodium phosphate buffer at pH 7.0 than for those of Hb A

29 ate that was first dissolved in a 0.1-mmol/L sodium phosphate buffer at pH 7.6 and administered to th

30 ular weight of the proteins extracted with a sodium phosphate buffer containing 2.0% sodium dodecyl s

31 thyl phenylacetyl glucuronide (MPG) in 0.1 M sodium phosphate buffer in D2O at pD 7.4 over 18 h to mo

32 pH pulse produced by freeze-thawing in mixed sodium phosphate buffer induces the oligomerization of D

33 stabilizing agent (i.e., methylene blue and sodium phosphate buffer mixture), the in vitro stability

34 mV shift from CNTs to 7.4 atom % N-CNTs in a sodium phosphate buffer solution (pH 7.0) with 2.0 mM NA

35 n of single-strand DNA, 5'-ATGCTGATGC-3', in sodium phosphate buffer solution at 10 degrees C tempera

36 sition of peroxynitrite (OONO(-)) in aqueous sodium phosphate buffer solution at neutral pH was inves

37 ents of glucose-isomerase concentration in a sodium phosphate buffer that is actively varied over the

38 um dodecyl sulfate from proteins in water or sodium phosphate buffer was achieved by column chromatog

39 Also, when sodium phosphate buffer was used, increasing the ionic s

40 (1.0 mM to 0.10 muM bilirubin, measured in a sodium phosphate buffer with pH 8.6) covers the clinical

41 oward neutral to slightly acidic pH in 10 mM sodium phosphate buffer, mitigating the concern of disas

42 ns of our assay (0.05 M sodium citrate/0.1 M sodium phosphate buffer, pH 5.25, 0.2 M NaCl, 0.1 mM EDT

43 el adopts a random-coil conformation in 2 mm sodium phosphate buffer, pH 5.5, and becomes an alpha he

44 With increasing hydration (50 mM sodium phosphate buffer, pH 7.0; 50 mM NaCl), T(M) decre

45 mbda em = 393 nm) in Tris buffer, pH 9.0, or sodium phosphate buffer, pH 7.2, but under the same cond

46 , 0.01-0.06 mM] but not in 0.14 M NaCl/10 mM sodium phosphate buffer, pH 7.2/0.5 mM CaCl2/0.15 mM MgC

47 of 1.0 mug muL(-1) stock solutions in 100 mM sodium phosphate buffers (pH 1-12) at room temperature.

48 genes encoding the kidney-specific type IIa sodium phosphate co-transporter (SLC34A1), the calcium-s

49 The sodium phosphate co-transporters Npt2a and Npt2c play im

50 that scaffolds membrane proteins, including sodium-phosphate co-transport protein 2A (NPT2A) at the

51 Sodium-phosphate co-transporter 2a (NaPi2a) is predomina

52 reduction in the protein levels of the renal sodium-phosphate co-transporter NaPi-IIa in the proximal

53 layed higher renal protein expression of the sodium-phosphate co-transporter NaPi-IIa, lower renal Kl

54 deficiency in the pulmonary epithelial Npt2b sodium-phosphate co-transporter that results in accumula

55 intra-erythrocyte delivery of dexamethasone sodium phosphate compared with placebo in children with

56 was dependent on alkyl side chain length and sodium phosphate concentration, but the same effects wer

57 ues were then minced and extracted with 5 mM sodium phosphate containing 1% Triton X-100.

58 Parathyroid hormone inhibits sodium-phosphate cotransport in proximal renal tubule ce

59 yroid hormone inhibits proximal renal tubule sodium-phosphate cotransport through a signaling complex

60 ogic regulator of proximal renal tubule cell sodium-phosphate cotransport, stimulates several signal

61 The sodium/phosphate cotransport inhibitor phosphonoformic a

62 Na-H exchanger 3, Na-K ATPase, and type IIa sodium phosphate cotransporter (NaPi IIa).

63 s a carboxy-terminal PDZ ligand required for sodium phosphate cotransporter 2a (NPT2A) and sodium hyd

64 panning protein that functions as a type III sodium phosphate cotransporter and as the receptor for a

65 hybridize to the message for the rat kidney sodium phosphate cotransporter NaPi-2 close to the trans

66 evels and decreased kidney membrane type IIa sodium phosphate cotransporter protein, as was the case

67 ranscripts for hBNP-1, a type 1b human brain sodium phosphate cotransporter, and cystic fibrosis tran

68 Human PiT1 (PiT1), another type III sodium phosphate cotransporter, is a highly related prot

69 on of phosphate uptake and PTH regulation of sodium-phosphate cotransporter (NaPi-4) expression were

70 ein (AKAP) by demonstrating that the type II sodium-phosphate cotransporter (NaPi-4) physically assoc

71 expression of the major apical transporters sodium-phosphate cotransporter 2A (NaPi-IIa) and sodium-

72 ising candidate gene, SLC34A1 encoding renal sodium-phosphate cotransporter 2A (NaPi-IIa), revealed a

73 The renal sodium-phosphate cotransporter 2a (Npt2a) plays an impor

74 sive genes, we inadvertently discovered that sodium-phosphate cotransporter 2B (NaPi-2b) mRNA concent

75 med by co-transfecting HEK293 cells with the sodium-phosphate cotransporter and wild type AKAP, a mut

76 in D 1alpha-hydroxylase cytochrome P450, and sodium-phosphate cotransporter mRNA concentrations.

77 ontains SLC34A3, the gene encoding the renal sodium-phosphate cotransporter NaP(i)-IIc.

78 (a) The proximal sodium-phosphate cotransporter NaPi-2 was markedly upreg

79 FGF23 levels and abundant expression of the sodium-phosphate cotransporter Npt2a at the brush border

80 n of recombinant cKL downregulated the renal sodium-phosphate cotransporter Npt2a in alphaKL-null mic

81 The sodium-phosphate cotransporter NPT2a plays a key role in

82 The sodium-phosphate cotransporter Npt2a, which mediates a l

83 bsorption of phosphate by downregulating the sodium-phosphate cotransporter Npt2a.

84 o bound other cellular targets including the sodium-phosphate cotransporter type IIa encoded by the N

85 sis transmembrane conductance regulator, and sodium-phosphate cotransporter type IIa.

86 also measured the expression of aquaporin-2, sodium/phosphate cotransporter (NaPi)-2, paracellin-1, a

87 ssociated with increased renal expression of sodium/phosphate cotransporter 2a (NaPi2a) protein.

88 The PIT1/SLC20A1 protein, a well-described sodium/phosphate cotransporter and retrovirus receptor,

89 mice have increased renal expression of the sodium/phosphate cotransporter NaP(i)2a and of 1- alpha-

90 se in the transport activity of the type IIa sodium/phosphate cotransporter protein (NaPi) despite an

91 The widely expressed mammalian sodium/phosphate cotransporter SLC20A1/PiT1 mediates pho

92 ses suggest that increased renal activity of sodium-phosphate cotransporters (NaPi2a) leads to severe

93 s in the SLC34A1 and SLC34A3 genes, encoding sodium-phosphate cotransporters 2a (NPT2a) and 2c (NPT2c

94 xcretion by reducing expression of the renal sodium-phosphate cotransporters NaPi-IIa and NaPi-IIc in

95 GF23 and small molecule inhibitors of kidney sodium-phosphate cotransporters.

96 Despite lower levels of the sodium/phosphate cotransporters (NaPi)-2a and -2c, knock

97 ace amounts of solutes with hydroxyl groups (sodium phosphate dibasic, potassium phosphate monobasic,

98 to high-dose intra-erythrocyte dexamethasone sodium phosphate did not initiate treatment.

99 PLGA) nanoparticles containing dexamethasone sodium phosphate (DSP) exhibited a size of 200 nm, 8 wt.

100 soluble form of dexamethasone, dexamethasone sodium phosphate (DSP), that has been demonstrated to ac

101 Here, we developed dexamethasone sodium phosphate (DSP)-loaded dicarboxyl-terminated poly

102 imizations revealed that sodium carbonate or sodium phosphate followed by DHB sublimation increases t

103 d 118 consecutive patients given single-dose sodium phosphate for bowel catharsis and 115 consecutive

104 8.6% (627 of 708) of colonic segments in the sodium phosphate group and in 88.1% (608 of 690) in the

105 ntly different between magnesium citrate and sodium phosphate groups (790 HU +/- 216 vs 978 HU +/- 16

106 weak chromatosome protection, but in 250 mM sodium phosphate has a structure very similar to that of

107 Here, we evaluated dexamethasone sodium phosphate-loaded platelet-inspired nanoparticles

108 The activity of cell-surface sodium-phosphate (Na(+)-P(i)) cotransporters mediates th

109 Apically expressed sodium-phosphate (Na(+)-P(i)) transporters play a critic

110 dministered pegylated liposomal prednisolone sodium phosphate (Nanocort) was compared to equipotent i

111 to receive either 2 mL (8 mg) dexamethasone sodium phosphate or 2 mL of IV solution (placebo) before

112 sphorylated or acetylated by Ac~P and either sodium phosphate or potassium phosphate, which are not p

113 , 2.60; 95% confidence interval, 1.46-4.63), sodium phosphate (OR, 9.34; 95% confidence interval, 2.1

114 ly 14-22 mg) intra-erythrocyte dexamethasone sodium phosphate, or placebo, using an independent inter

115 Oral sodium phosphate (OSP) is a commonly used purgative befo

116 t formation, autolyzed more rapidly in 10 mM sodium phosphate (pH 6.8), and, in contrast to strains t

117 In 10 mM sodium phosphate (pH 7), the GI domain, like the globula

118 Likewise, the formation of alanine in 500 mM sodium phosphate (pH 7.0) from 5 mM glyceraldehyde and 1

119 yde and ammonium ion in aqueous solutions of sodium phosphate (pH 7.0) or imidazole-imidazolium chlor

120 Surprisingly, in 10 mM sodium phosphate (pH 7.0), GII is largely unfolded, wher

121 dodecyl sulfate (SDS) and 1-butanol in 10 mM sodium-phosphate (pH 7.2) at a flow rate of 5 mL/min.

122 sensitivity and speed of analysis were 50 mM sodium phosphate, pH 2.3, and 100 mM ammonium formate, p

123 roximately 2 microM at 25 degreesC in 0.1 mM sodium phosphate, pH 7.2.

124 ibrils after incubation (37 degrees C, 10 mM sodium phosphate, pH 7.60), but in contrast to beta-shee

125 embranes prepared by hypotonic lysis in 5 mM sodium phosphate, pH 8.0 (5P8), conditions in which the

126 oscopy, including polyethylene glycol (PEG), sodium phosphate, picosulfate, or oral sulfate solutions

127 Phenstatin was converted to the sodium phosphate prodrug (3d) by a dibenzyl phosphite ph

128 Hydroxyphenstatin was converted to the sodium phosphate prodrug (6e) by a dibenzyl phosphite ph

129 oscopy preceded by bowel cleansing with oral sodium phosphate solution (OSPS) or Visicol.

130 These viruses use the related sodium-phosphate symporters Pit1 and Pit2, respectively,

131 multicenter trial compared 1.0% prednisolone sodium phosphate to placebo in the treatment of bacteria

132 genes with structural similarity to a type 1 sodium phosphate transporter, 12 novel histone genes, an

133 nic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter 2a and 2c are rare causes o

134 delivery (PBS pH 7.2 and 0.9% saline), and a sodium phosphate vehicle previously shown to enhance the

135 fference seen in the sigmoid colon (2.17 for sodium phosphate vs 2.44 for magnesium citrate; P< 0.01)

136 Intravenous intra-erythrocyte dexamethasone sodium phosphate was administered once a month for 6 mon

137 When sodium phosphate was substituted for beta-glycerol phosp

138 intra-erythrocyte delivery of dexamethasone sodium phosphate will continue in participants aged 6-9

139 In 10 mM sodium phosphate with 125 mM NaCl, the combinations of s

140 II-L is very similar to GII folded in 250 mM sodium phosphate, with the exception of the substituted

141 1 M triflic acid) and 1150 mV at pH 6 (10 mM sodium phosphate) yielded a red colored solution with a