ライフサイエンスコーパス: periodate

1 ished by treatment of the glycopeptides with periodate.

2 ith hydrogen peroxide, air oxygen, or dilute periodate.

3 to o-aminophenols in the presence of sodium periodate.

4 s secondary alcohols, at specified levels of periodate.

5 hloride and subsequent oxidation with sodium periodate.

6 were subjected to oxidation by tyrosinase or periodate.

7 ses, and unaffected by oxidation with sodium periodate.

8 atment of T. vaginalis with metronidazole or periodate abolished the adhesion of parasites to cell mo

9 of binding to MAb 1B5 whereas treatment with periodate abolished this binding, suggesting the presenc

10 oelectric point of 4.2-4.6, and was shown by periodate acid Schiff's staining to be glycosylated.

11 as highly selective fluorescence sensors for periodate amongst a set of different anions.

12 elective interaction of peanut proteins with periodate amongst chloride, sulphate, iodide, phosphate,

13 s abolished by pretreatment of sections with periodate and in the presence of excess sialic acid or l

14 etected by oxidization of carbohydrates with periodate and labeling with hydrazide-conjugated digoxig

15 chment of terminal glycerol for oxidation by periodate and reaction of the resulting aldehyde with am

16 mmediately fixed in paraformaldehyde, sodium periodate, and lysine (PLP); (2) some were stored at 4 d

17 HA with periodate- and neuraminidase-treated RBCs indicated that

18 hlorite, hydrogen peroxide, ozone and sodium periodate, are described in this review.

19 e couplings with anilines in the presence of periodate as oxidant.

20 M 3 binding when specimens were treated with periodate at high pH, which specifically destroys NeuPSA

21 A periodate based oxidation was performed for an AHB-based

22 urface-displayed mannan by acid treatment of periodate-borohydride cells exposes glucan.

23 nnan-dependent resistance can be overcome by periodate-borohydride conversion of mannose polysacchari

24 charides to polyalcohols; cells treated with periodate-borohydride initiate the alternative pathway w

25 Pretreatment of mucin with periodate but not with pronase reduced adherence.

26 posure of C. pneumoniae elementary bodies to periodate, but not elevated temperatures, inhibited chol

27 d be demonstrated that iodate is oxidized to periodate by a CuO-activated hypohalous acid, which is a

28 amine oxidized with one equivalent of sodium periodate causes a concentration-dependent inactivation

29 oretic methods and by controlled cleavage at periodate-cleavable moieties incorporated during synthes

30 oretic methods and by controlled cleavage at periodate-cleavable moieties incorporated during synthes

31 D(3) by comigration on two HPLC systems and periodate cleavage reaction.

32 Comigration on two HPLC systems, periodate cleavage reactions, and NaBH4 reduction establ

33 We found that low levels of periodate, commonly used to oxidize specifically termina

34 No periodate could be measured in filtered solutions becaus

35 oprotein P by N-glycosidase assay and by the periodate-dansylhydrazine test, which indicated no detec

36 , oxidation of the mucin glycans in pLL with periodate did not abrogate the effects on cells.

37 d oxidation with hydrogen peroxide or sodium periodate (i.e., the phenylselenocysteine side chain is

38 roduct 4 was oxidatively cleaved with sodium periodate in the presence of methylamine.

39 bilizes developing charge on both sulfur and periodate in the transition state via cation-pi and elec

40 It is sensitive to pronase and periodate, indicating that it is likely a glycoprotein.

41 ut were susceptible to treatment with sodium periodate, indicating that the antigen inducing opsonic

42 Using mildly basic reaction conditions, the periodate-induced diol cleavage of meso-tetraphenyl-2,3-

43 Second, we demonstrated that periodate-induced DOPA-protein cross-linking could be ca

44 The protein periodate interactions have also resulted in a simultane

45 ylazo dienophiles with tetra-n-butylammonium periodate is reported.

46 ced by 3,4-dihydroxyphenylalanine (DOPA) for periodate-mediated chemical cross-linking, and biotin wa

47 Erosion of the inner shell via periodate-mediated cleavage of the 1,2-diol bond in DHEA

48 oupled receptor (GPCR), has been analyzed by periodate-mediated cross-linking.

49 The method involves the periodate-mediated reaction of phenylene diamine substit

50 as determined using a murine model of sodium periodate (NaIO(4))-induced peritonitis.

51 otocol that can greatly reduce the amount of periodate necessary for effective coupling.

52 xyfunctionalization of steroidal ethers with periodate or bromate as terminal oxidants in phosphate b

53 chains of cell surface Sia residues by mild periodate oxidation (known to abrogate Sia recognition b

54 ion with ethylthioacetyl chloride and sodium periodate oxidation afforded a E/Z mixture of alpha-sulf

55 two novel procedures: triethylamine-assisted periodate oxidation and acetolysis.

56 ribe a technique termed GLIB (glucosylation, periodate oxidation and biotinylation), which combines s

57 emical modification of a standard heparin by periodate oxidation and borohydride reduction enhanced i

58 ivatives of digoxin have been synthesized by periodate oxidation and reductive amination using a vari

59 after modification of the GalNAc residues by periodate oxidation and sodium borohydride reduction, in

60 ides were monitored for activation by sodium periodate oxidation and subsequent analysis by gas chrom

61 bstituted, peptide-linked GalNAc residues by periodate oxidation and subsequent trimming of the remai

62 The lesion is released via periodate oxidation of a triol containing a vicinal diol

63 etal-dependent hydroxyquinone formation from periodate oxidation of catechol 1, suggested a rate-limi

64 The periodate oxidation of paralytic shellfish toxins (PSTs)

65 Mild periodate oxidation of sialic acids to their correspondi

66 try, frequent use is made of formaldehyde by periodate oxidation of terminal vicinal diols.

67 lboronate was achieved in part by controlled periodate oxidation of the 9,21-diol to the 21-nor-9-oxo

68 ily the exoplasmic leaflet as detected using periodate oxidation of the cell surface.

69 3) of triacylglycerol was measured following periodate oxidation of the glycerol isolated from hydrol

70 Mild periodate oxidation of the L-selectin ligand CD34, or L-

71 advance for assessing specificity using mild periodate oxidation of the sialic acid chain.

72 Under the same conditions, periodate oxidation of the simple catechol 4-tert-butylc

73 The in situ periodate oxidation of the unstable N-hydroxyphosphorami

74 Periodate oxidation of this lactam led directly to an al

75 The strategy includes periodate oxidation of tryptic digests, solid-phase enri

76 pald reagent, especially in conjunction with periodate oxidation reactions.

77 l nucleic acid ribosides, such as ATP, using periodate oxidation simplifies the chromatogram and mini

78 The results of periodate oxidation studies suggested that the product f

79 ethylated and 2'-hydroxylated nucleosides to periodate oxidation to develop Nm-seq, a sensitive metho

80 The method uses mild periodate oxidation to generate an aldehyde on sialic ac

81 by labeling with biotin hydrazide following periodate oxidation, a specific and well established met

82 first approach, termed GLIB (glucosylation, periodate oxidation, biotinylation) uses a combination o

83 four monokines were found to be sensitive to periodate oxidation, the TNF-alpha-stimulating activity

84 on of FT-IR, methylation and GC-MS analysis, periodate oxidation-Smith degradation, partial acid hydr

85 used as substrates for galactose oxidase and periodate oxidation.

86 nd rapidly converted to the aldehyde form by periodate oxidation.

87 (DOPA) as a protein cross-linking agent upon periodate oxidation.

88 ins, and reactivity with hydrazide following periodate oxidation.

89 ylsulfeny)acetyl chloride followed by sodium periodate oxidation.

90 Limited periodate oxidations suggested that the +258-Da modifica

91 blocked by P2X7RS-specific concentrations of periodate oxidised ATP (OxATP: 100 microM) and brilliant

92 ophages with a P2Z/P2X7 receptor antagonist, periodate oxidized adenosine 5'-triphosphate (o-ATP), su

93 receptor antagonists, including suramin and periodate oxidized ATP (oATP), resulted in a significant

94 -2',4'-disulphonic acid, Brilliant Blue G or periodate oxidized ATP dialdehyde to the site of ATP rel

95 ct of the cross-linking reaction between the periodate-oxidized AMP moiety of the tRNA and Lys207 is

96 etween aldehyde groups on the Fc moieties of periodate-oxidized antibodies and hydrazide groups on fu

97 tropic nucleotide (P2X) receptors, including periodate-oxidized ATP (oATP), attenuate a subset of end

98 In vivo short-term P2X7R targeting (using periodate-oxidized ATP [oATP]) delays islet allograft re

99 y the P2X(7) purinergic receptor antagonists periodate-oxidized ATP and pyridoxal-phosphate-6-azophen

100 ular ATP/P2X purinergic signaling pathway by periodate-oxidized ATP delayed the progression of the dy

101 Short-term P2X7R targeting with periodate-oxidized ATP promotes long-term cardiac transp

102 ed by the P2 receptor antagonists XAMR 0721, periodate-oxidized ATP, and suramin.

103 sion of IL-6 were revealed in the muscles of periodate-oxidized ATP-treated mdx mice.

104 nnective tissue growth factor, in muscles of periodate-oxidized ATP-treated mdx mice.

105 the P2X(7) receptor and that is inhibited by periodate-oxidized ATP.

106 This reagent reacted rapidly with periodate-oxidized N-terminal Ser or Thr peptides and wi

107 ted enhanced macrophage and mast cell death; periodate-oxidized-ATP (oATP)-treated macrophage and mas

108 vivo perfusion with paraformaldehyde-lysine-periodate (PLP) and processed for light and electron mic

109 Furthermore, periodate reactivity of the final product signifies acqu

110 n good agreement with those from the current periodate-resorcinol method (P>0.05) thus indicating tha

111 iol (1) to Cu(II) and subsequent addition of periodate resulted in rapid formation of the TPQ-like co

112 dation but rather were obtained using sodium periodate, resulting in variable NDA yields (13-51%) fro

113 The periodate salts may garner widespread use in military an

114 Periodate sensing using different synthesized organic mo

115 ng a battery of monoclonal antibodies (MAbs) periodate-sensitive epitopes were identified on Tf190, s

116 of pneumococci with pronase E but not sodium periodate significantly reduced C1q binding.

117 ody that was serovar specific for Oag and by periodate-silver staining.

118 Using both thin-layer chromatography and the periodate-thiobarbituric acid reaction, we found that th

119 When a 2:1 molar ratio of periodate to alditol is used, the core mannitol is cleav

120 f the sulfide derivatives were oxidized with periodate to give their corresponding sulfones.

121 )glycero-d-manno-heptose of LPS molecules by periodate to release formaldehyde.

122 could be generated in situ by oxidation with periodate (to avoid generation of H(2)O(2)).

123 Periodate-treated ehrlichiae did not induce production o

124 Periodate-treated parasites showed no adherence to host

125 hand, lymphocytes from mice sensitized with periodate-treated SEA did not produce any of these same

126 Mice sensitized with periodate-treated SEA displayed a significant decrease i

127 Furthermore, sensitization of mice with periodate-treated SEA significantly reduced levels of Ag

128 ice sensitized with native SEA, but not with periodate-treated SEA, produced IL-4, IL-5, and IL-10 wh

129 Metronidazole- or periodate-treated T. foetus showed no damage to BVEC mon

130 those containing a cP, are cleaved through a periodate treatment after phosphatase treatment; hence,

131 ective cleavage at the core mannitol by mild periodate treatment and analysis of the reaction product

132 region, which were missing from the mutants; periodate treatment and carbohydrate staining confirmed

133 s sensitive to proteinase K and resistant to periodate treatment and glycoprotein staining.

134 t treatment of E. chaffeensis had no effect, periodate treatment completely abolished the ability of

135 ees C for acid hydrolysis of PS precedes the periodate treatment in the purpald assay.

136 Heat or proteinase K treatment but not periodate treatment of E. chaffeensis abrogated the inhi

137 Periodate treatment of lysates of the clone confirmed th

138 Periodate treatment of MG2 did not affect the interactio

139 Binding of MAb 4A4-2 was inhibited by mild periodate treatment of N. caninum antigen, demonstrating

140 Periodate treatment of recombinant gp36 reduced the anti

141 the synthetic (nonglycosylated) peptide, and periodate treatment of the recombinant glycopeptide epit

142 nsitive to proteinase K treatment but not to periodate treatment, indicating that the cognate epitope

143 rformance liquid chromatography analysis and periodate treatment.

144 ost with proteinase K treatment but not with periodate treatment.

145 e Man alpha(1-3)Man branch was oxidized with periodate under controlled conditions.

146 The adsorbed periodate was identified by scanning electron microscopy

147 In this approach, periodate was used under mild conditions to oxidize the

148 eness of modification of sialic acid by mild periodate was verified with monoclonal antibody to sialy

149 The interactions of the proteins with periodate were also confirmed by other spectral methods

150 Further, treatment of R36A with periodate, which selectively destroys PC residues, had n