ライフサイエンスコーパス: Tris

1 Tris (dibenzylideneacetone) dipalladium (Tris DBA), a sm

2 Tris DBA improved ASLN in mice through immunoregulation

3 Tris(1,3-dichloro-2-isopropyl) phosphate (TDCIPP) concen

4 Tris(1,3-dichloro-2-propyl) phosphate (TDCIPP) has been

5 Tris(1,3-dichloro-2-propyl)phosphate (TDCIPP) is a high-

6 Tris(1,3-dichloro-2-propyl)phosphate (TDCIPP) is a high-

7 Tris(1,3-dichloroisopropyl)phosphate (TDCIPP) was the mo

8 Tris(1-chloro-2-propyl) phosphate (TCIPP) was the most a

9 Tris(2,2'-bipyridyl)ruthenium can be excited to fluoresc

10 Tris(2-aminoethylamine) and cis-1,3,5-tris(aminomethyl)c

11 Tris(2-benzimidazolylmethyl)amines have been found to be

12 Tris(2-butoxylethyl) phosphate (TBOEP) accounted for 40%

13 Tris(2-carboxyethyl)phosphine (TCEP) is a widely used su

14 Tris(2-pyridylthio)methane, [Tptm]H, has been employed t

15 [Tris(2-pyridylthio)methyl]zinc fluoride, [kappa(4)-Tptm]

16 [Tris(2-pyridylthio)methyl]zinc hydride, [kappa(3)-Tptm]Z

17 Tris(8-quinolinolato)gallium(III) (1, KP46) is a very pr

18 Tris(beta-diketimine) cyclophanes are an important ligan

19 Tris(chloropropyl) phosphate isomers (SigmaTCPP) account

20 Tris(heterocyclemethyl)amines containing mixtures of 1,2

21 Tris(ligand) iron(III) complexes were prepared and inves

22 Tris(pentafluorophenyl)boron B(C6F5)3 is an effective ca

23 Tris(phenylthio)benzene molecules have been synthesized

24 Tris(phosphine)borane ligated Fe(I) centers featuring N(

25 Tris(quinolinolate)aluminum(III) (AlQ3) is the most wide

26 Tris(silyl) calixarene 7 was assigned the flattened cone

27 Tris(trialkylsilyl)silyl groups are easily prepared and

28 Tris(trifluoropropyl)trimethyl-cyclotrisiloxane and tetr

29 Tris(trimethylsilyl)amine is formed with an initial turn

30 Tris(trimethylsilyl)sulfonium 1 and methylbis(trimethyls

31 Tris(triphenylphosphinegold) oxonium tetrafluoroborate,

32 Tris-(1-chloro-2-propyl)phosphate (TCPP) was the most ab

33 Tris-arenes based on either isophthalic acid or 2,6-dipi

34 Tris-based buffers, even in optimal form, create a runaw

35 Tris-borate has a high-buffering capacity and is therefo

36 Tris-hydroxymethyl aminomethane (THAM) may be an effecti

37 Tris[N,N-bis(trimethylsilyl)amide]lanthanum (La(NTMS)) i

38 ine (PBS) buffers was similar, but in pH 8.0 Tris the hydrolysis rate nearly doubled.

39 ) M p-nitrophenyl phosphate in 1.0 M, pH 9.0 Tris buffer as the substrate for the enzymatic reaction,

40 nd an s of 5 bp were obtained in 5 mM pH 7.1 Tris-HCl buffer solution containing 50 mM NaCl.

41 the melting temperatures suggests that 0.15 Tris+ ion per phosphate is released upon denaturation.

42 d optimum response within 2s at pH 8.5 (0.1M Tris-HCl) and 35 degrees C, when operated at 20 mV s(-1)

43 A low-ionic-strength solution, 6.1muS/cm 1mM Tris (pH 9.3), was used to produce ACEO and proved the f

44 CEO driving and DNA hybridization in the 1mM Tris solution were 1.5 Vpp and 200Hz.

45 n the singly reduced form, BV*+, in a pH 7.4 Tris-HCl buffer solution at mu = 8.4 mM.

46 ted trigonal pyramidal building block, 1,3,5-Tris(4-aminophenyl)adamantane, with linear dialdehyde bu

47 2,4,6-Tris(chlorosulfonyl)aniline (47) was obtained by the chl

48 2,4,6-Tris(dimethylamino)-1,3,5-triazine was prepared to compl

49 MAC was achieved with crude extract at pH 7, Tris-HCl binding buffer at pH 7 and the use of 300 mM im

50 nt of a 1,4,7,10-tetraazacyclododecane-1,4,7-Tris-acetic acid ligand to bind (64)Cu(2+).

51 ffers/pH (potassium phosphate buffer pH 6-8, Tris buffer pH 8-10) on the current responses generated

52 A Tris-Acetate-Phosphate-Pluronic (TAPP) medium that under

53 cally injected into a capillary containing a Tris-based aqueous buffer.

54 iding x-ray characterization of As(III) in a Tris thiolate protein environment and allowing a structu

55 on was also carried out into the effect of a Tris-HCl buffer containing the surfactant Tween 20 to ai

56 nks fluorescein and rhodamine dyes through a Tris[(2-pyridyl)methyl]amine bridge.

57 igher separation resolution as compared to a Tris glycine system, destacking of proteins down to 6.5

58 uidic Western blot assay (muWestern) using a Tris tricine discontinuous buffer system suitable for an

59 mM), is separated using such a column with a Tris buffer.

60 ion (>200 mM) of the chemical reducing agent Tris(2-carboxyethyl)phosphine (TCEP) as its reduction ra

61 since the disulfide-specific reducing agent Tris(2-carboxyethyl)phosphine hydrochloride failed to su

62 odiglycol) or the non-sulphur reducing agent Tris-(2-carboxylethyl)phosphine (TCEP).

63 ther confirmed by its resistance to alkaline Tris.HCl.

64 presence of tris(hydroxymethyl)aminomethane (Tris).

65 ct is strongly ion-specific, with Ca(2+) and Tris, respectively, promoting and reducing stress-induce

66 Li(+), NH(4)(+), and Tris(+) ions bind to A-tracts with similar affinities; t

67 s solutions containing NaCl, KCl, CaCl2, and Tris buffer show that the magnitude of the effect is str

68 e presence of Na(+), K(+), Li(+), Ch(+), and Tris(+) and that the catalytic efficiency of prothrombin

69 A-binding activity, while cytochalasin D and Tris decreased both F-actin and NPA-binding activity in

70 sponses by the reductants dithiothreitol and Tris(2-carboxyethyl)phosphine (TCEP).

71 as been measured in diethylmalonate (DM) and Tris-acetate buffers, with and without added NaCl or Tri

72 from TB patients preserved with K(2)EDTA and Tris-EDTA, respectively, showed significantly lower medi

73 red by brief illumination of O2 evolving and Tris-washed preparations at 200 K or by a single saturat

74 Similar glycerol and Tris derivatives as well as dNMPs were also formed with

75 In the presence of dATP, glycerol, and Tris buffer, the DNA primase isolated from Thermococcus

76 However, Hepes and Tris buffers did not allow formation of NO-Fe(DTCS)2.

77 ed that comigrates on reverse phase HPLC and Tris-tricine electrophoresis.

78 rs of hKAT I: indole-3-acetic acid (IAC) and Tris.

79 n of K(+), Ba(2+), Mg(2+), Na(+), Li(+), and Tris(+) in approximately 30 s, with efficiencies greater

80 y(ethylene glycol) acrylate/methacrylate and Tris-HCl buffer was loaded into the microdevice.

81 chelators 2-mercaptopropionic acid (MPA) and Tris-EDTA (TE) to detect MBLs.

82 Phosphate and Tris-HCl buffers decrease the signal intensity measured

83 ox species [Ru(NH3)6](3+/2+) for pumping and Tris buffer, was transported by redox-MHD and detected w

84 e membrane (CEM) -based anion suppressor and Tris and ethylenediamine buffers using an anion-exchange

85 prevented by anti-AbetaP antibody, zinc, and Tris, but not by tachykinin neuropeptides.

86 f a sample that contains a weak base such as Tris (pK(a) = 8.2) is presented here for the first time.

87 effects of common buffer components, such as Tris and glycerol, on the biotinylation process.

88 Because Tris is able to occupy the substrate binding position, w

89 The structurally biomimetic Tris-imidazole model is the most selective.

90 Commercial Bis-Tris-Mes gels provide a sample reduction buffer at pH 8.

91 219 +/- 9.7 mumol/min/mg by using HEPES-Bis-Tris propane, pH 7.5.

92 V) bis-Tris propane (1.0014) and Eu(III) bis-Tris propane (1.0012).

93 iethanolamine/Tricine, pH 7.9; and (iii) Bis-Tris/Aces, pH 6.7.

94 The preparation of cell-free extract in Bis-Tris propane/HCl, pH 7, buffer containing 0.025% (w/v) T

95 Rates are significantly lower in Bis-Tris-Mes gels than in Tris-glycine gels, reducing the ri

96 oester p-nitrophenyl phosphate by Ce(IV) bis-Tris propane (1.0014) and Eu(III) bis-Tris propane (1.00

97 fect on the reaction catalyzed by Ce(IV) bis-Tris propane solutions at pH 8 was determined to be 1.00

98 xidized to Fe3+ at 37 degrees C in 20 mM Bis-Tris buffer at pH 5.8, was significantly slowed in the p

99 in the presence of 100 mM KCl and 10 mM Bis-Tris propane over a pH range of 6.00-8.00.

100 conditions employed in this study (10 mM Bis-Tris, 200 mM KCl, 2.5 mM MgCl(2), 1 mM CaCl(2), 100 micr

101 The concentration of bis-Tris buffer impacts the extent of coupling of oxygen act

102 is determined to be 9.5, in contrast to Bis-Tris-Mes gels where the pH is 7.2.

103 The evidence includes structures with Bis-Tris (2,2-bis(hydroxymethyl)-2,2',2''-nitrilotriethanol)

104 e preparation at the higher pH used with Bis-Tris gels.

105 By testing the device with both Tris buffer and artificial urine containing a wide range

106 the homes, we detected TDBPP, or brominated "Tris," which was banned in children's sleepwear because

107 ansition Tg in a freeze-concentrated buffer (Tris-HCl).

108 m formate) with a near-physiological buffer (Tris-acetate) for three protein-ligand pairs.

109 y unfavorable interactions between the bulky Tris-borate ion and RNA or partial coordination of RNA f

110 hKAT-I is inhibited by Tris under physiological pH conditions, which explains w

111 nzymes by their sensitivity to inhibition by Tris and free arginine.

112 carried out by varying the pH maintained by Tris-HCl or CAPS buffer (pH 8.0 and 10.3) and keeping th

113 and is inhibited in a competitive manner by Tris buffer.

114 After disruption of the outer membrane by Tris-EDTA-lysozyme, the inner-membrane-anchored proteins

115 hen part of the external Na+ was replaced by Tris.

116 Hence, positively charged Tris buffer ions will compete with other monovalent cati

117 r testing by quantitative PCR were compared: Tris-EDTA (TE) buffer, PrepMan Ultra, 2% sodium dodecyl

118 Under some conditions, Tris-borate is a poor counterion for RNA and its use mer

119 t mixture, buffered at pH 7.8 and containing Tris, Triton X-100, glucose-6-phosphate, nicotinamide ad

120 conditions (conventional buffer: containing Tris and higher Mg2+ concentration [10-15 mM]; and polya

121 ll as otherwise identical buffers containing Tris.

122 The pH of conventional Tris-glycine SDS-PAGE gels during a run is determined to

123 esonance imaging (MRI) contrast agent, CREKA-Tris(Gd-DOTA)3 (Gd-DOTA (4,7,10-tris(carboxymethyl)-1,4,

124 Here we assess the capability of CREKA-Tris(Gd-DOTA)3 to detect micrometastasis with MRI in co-

125 We find that CREKA-Tris(Gd-DOTA)3 provides robust contrast enhancement in t

126 ts demonstrate that molecular MRI with CREKA-Tris(Gd-DOTA)3 may facilitate early detection of high-ri

127 Synthesis of the sterically crowded Tris(pentamethylcyclopentadienyl) lanthanide complexes,

128 at were identified as dAMP-glycerol and dAMP-Tris.

129 Small isolated protofibrils in dilute Tris-HCl buffers were directed along the elongation path

130 Tris (dibenzylideneacetone) dipalladium (Tris DBA), a small-molecule palladium complex, has been

131 he disulfide-reducing agents dithiothreitol, Tris(2-carboxyethyl)phosphine (TCEP), or reduced glutath

132 aks in 20-80 mM TAE (TAE, Tris-acetate-EDTA; Tris, tris[hydroxymethyl]aminomethane) buffer.

133 ly performed using buffers containing either Tris, acetate, and EDTA (TAE) or Tris, borate, and EDTA

134 roxylations of benzyl alcohol, ethylbenzene, Tris buffer, lauric acid, and methyl laurate and epoxida

135 High-performance explosives: Tris(triazolo)benzene was synthesized and converted to i

136 tial and temporal distribution are given for Tris-(1-chloro-2-propyl) phosphate (TCiPP), EHDPP, tri-n

137 ase pair (bp) oligomer ranged from 71 mM for Tris+ to 173 mM for Na+ and K+.

138 .3 A X-ray structure of the GDPMH-Mg(2+)-GDP.Tris(+) complex, the GDP leaving group interacts with fi

139 was permeable to Na(+) approximately K(+) >> Tris(+), and whole-cell current density at -80 mV increa

140 action procedures, including the use of HCl, Tris-HCl buffer, and enzymatic hydrolysis (using protein

141 examined (substituted imidazoles, histidine, Tris, and 1,4-diazabicyclo[2.2.2]octane).

142 with o-phenanthroline and eosin at pH 7.5 in Tris; a piece of filter paper was used as a solid suppor

143 orm of holoShp (hemoShp) is stable in air in Tris-HCl buffer, pH 8.0, binds to apoHtsA with a K(d) of

144 A and PNA (peptide nucleic acid) beacons, in Tris-buffer solutions containing various concentrations

145 At 25 degrees C in Tris at pH 8.3, MutL assembles into a heterogeneous mixt

146 ill compete with other monovalent cations in Tris-buffered solutions.

147 validated by correctly sensing pH changes in Tris and acetate solutions.

148 In contrast, in Tris-borate, RNA collapse has a much smaller apparent Mg

149 en 20) and Cetylpyridinium chloride (CPC) in Tris/HCl buffer, pH 8.5.

150 een VAL and Li(+), Na(+), K(+), and Cs(+) in Tris buffer solution were determined to be 67+/-42, 120+

151 face charge density were subjected to CZE in Tris-HCl (pH 8) buffers of various ionic strengths (0.00

152 een measured by capillary electrophoresis in Tris-acetate buffer, to test the hypothesis that site-sp

153 er nucleotides increase the rate >20-fold in Tris buffer.

154 Msp(Fl) folded in Tris buffer contained slightly less beta-sheet structure

155 glass surfaces, RCA-cleaned and immersed in Tris-EDTA buffer were also studied.

156 ncated at D421 was detected at low levels in Tris-soluble and detergent-soluble tau at 3 to 6 months

157 zine synthase with a Ki of 66+/-13 microM in Tris buffer and 22+/-4 microM in phosphate buffer.

158 one-4-phosphate substrate from 5.2 microM in Tris buffer or from 6.7 microM in MOPS buffer to 50 micr

159 trypsin ranging from 0.002 to 2 microg/ml in Tris-buffered saline buffer for 2 h.

160 egrees C and [Mg(2+)] approximately 10 mM in Tris-borate (TB) buffer.

161 ic strengths, it could be easily observed in Tris buffer, containing 150 mM NaCl.

162 oximately 3.75 wt % linear polyacrylamide in Tris-HCl) is used to obtain fully stretched configuratio

163 s and calibration standards were prepared in Tris buffer (pH:7.2) for selective hydride generation an

164 roximately 10 days), second-order process in Tris-buffered saline.

165 e containing the dipeptide glycyl-proline in Tris-HCl supplemented with manganese at 37 degrees C for

166 of inhibition and fluorescence quenching in Tris buffer occurs when an average of two serine binding

167 Screening of selenium in Tris-buffer-urea soluble fraction was carried out by sod

168 homogenization of the excised gel slice (in Tris-EDTA buffer), containing the DNA fragment of intere

169 cores, the Tg mice peptides were soluble in Tris-SDS-EDTA solutions, revealing both monomeric and SD

170 ) were used to characterize PHF suspended in Tris-buffered saline (TBS), sodium acetate buffer, and w

171 tidyl choline (DOPC) liposomal suspension in Tris-HCl buffer (pH 7.4 at 40 degrees C) has been develo

172 on of the rac-alcohols using W110A TESADH in Tris buffer/acetone (90:10, v/v).

173 moanaerobacter ethanolicus (W110A TESADH) in Tris buffer using 2-propanol (30%, v/v) as cosolvent and

174 However, when tested in Tris buffer vs Mycobacterium tuberculosis lumazine synth

175 ificantly lower in Bis-Tris-Mes gels than in Tris-glycine gels, reducing the risk of adventitious pro

176 fractional site occupancy indicates that in Tris buffer, one serine is bound to each interface at ma

177 We also show that in Tris-buffered solutions the Raman signature of supercoil

178 ay involves homogenization of the tissues in Tris-HCl:glycerol buffer and the recording of Soret exci

179 different DNA extraction methods, including Tris-EDTA Method, a modified Cetyltrimethylammonium Brom

180 correlated with (1) significantly increased Tris-buffered saline (TBS)-insoluble Abeta(42) levels an

181 nto random-coil structure upon dilution into Tris buffer.

182 ement over earlier model reactions involving Tris.

183 ay 3), injected CA II protein + Tris or just Tris (Day 3), measured I(NBC) or the initial rate at whi

184 d out in buffered medium (methanol: 10mmol/l Tris buffer pH 7.5, 1:1 v/v) and reaction was completed

185 In a solution containing 0.04 M Tris-acetate buffer at 25 degrees C, calculated mobiliti

186 is routinely stored at 4 degreesC, in 0.05 m Tris/HCl buffer containing 25% glycerol and at high prot

187 l(2) and 2.5 mM Ru(NH(3))(6) Cl(3), in 0.1 M Tris buffer (pH = 9).

188 In addition, the same measurements in 0.1 M Tris buffer at pH 7.0 show a much slower exchange rate f

189 ed wine after its dilution (4-fold) in 0.1 M Tris pH 8.0.

190 ine derivatives were well separated in 0.1 M Tris-0.1 M borate-2 mM EDTA buffer (pH 8.75) using a 60-

191 when operated at 0.2V (vs. Ag/AgCl) in 0.1 M Tris-HCl buffer, pH 8.5 and at 35 degrees C.

192 l peptides at pH 7.4, 37.0 degrees C, 0.15 M Tris.HCl buffer have been determined; a library of 913 a

193 In 0.20 M Tris buffer solution (pH 7.4), an irreversible, overlapp

194 s without an aminosulfonate moiety (maleate, Tris, and bicarbonate).

195 in the presence of NRS in a buffered medium (Tris; pH 8.0) with formation of Fe(II)/NRS complexes.

196 , 27% sucrose (wt/vol), 2 mM EDTA, and 10 mM Tris (pH 9), were required for efficient OM release, as

197 propylamine and O(2) as substrates in 10 mM Tris HCl, pH 7.9, 4 degrees C.

198 f 2400(+/-600) nt before dissociation (10 mM Tris-HCl (pH 8.3), 20 mM NaCl, 20% (v/v) glycerol, 25 de

199 potassium glutamate and 8 mM MgCl2 or 10 mM Tris-HCl and 200 mM KCl, with or without 0.5% Tween adde

200 e addition of glycerol to 500 mM NaCl, 20 mM Tris (pH 8.4), 2 mM beta-mercaptoethanol significantly e

201 by sodium borohydride (200 microm) in 20 mm Tris-HCl, 1 mm EDTA at 37 degrees C, pH 7.4, gives a 50-

202 were completed in less than 30 s using 25 mM Tris, 192 mM glycine at pH 8.5 as the electrophoresis bu

203 formed directly from a 150 mM KCl and 25 mM Tris-HCl buffer at pH 7 that is widely used in protein c

204 n even in the presence of 0.05% SDS in 25 mM Tris/HCl buffer, which indicated that it was highly asso

205 onditions [350 mM KCl, 8 mM MgCl2, and 30 mM Tris (pH 7.5)], a complex with an association constant o

206 e of 1.27 +/- 0.06 kcal mol(-1) M(-1) (30 mM Tris-HCl, pH 8, 1 mM DTT, 25 degrees C).

207 ation constant in our standard buffer (40 mm Tris (pH 7.9), 10 mm MgCl(2), 0.1 mm dithiothreitol, 5%

208 s were measured for eight oligomers in 40 mM Tris acetate buffer.

209 icrom C(18) packing with 75% ACN (v/v), 5 mM Tris at pH 8.0.

210 r Eu(III) (6.2 +/- 0.3 microM) (pH 7.8, 5 mM Tris) were determined by tryptophan fluorescence titrati

211 ere mobile phase containing 90/10 ACN/2.5 mM Tris, pH 8, sheath liquid containing 50/50 MeOH/10 mM HC

212 om virions disrupted by treatment with 50 mM Tris (pH 7.5), 0.5 M NaCl, 0.5% NP-40, and 10 mM dithiot

213 that Ms-Lon associates to a hexamer at 50 mM Tris and 10 mM MgCl(2), at pH 8.0 and 20 degrees C, and

214 ormation constants (in the presence of 50 mM Tris) of P3W for Eu(III) (K(a) = (2.1 +/- 0.1) x 10(5) M

215 sieving ability at 0.5% (w/w) in TTE (50 mM Tris, 50 mM TAPS, 2 mM EDTA, pH 8.4) buffer.

216 odiscs at 20 degrees C in 100 mM NaCl, 50 mM Tris, at pH 7.4.

217 electrolytes (BGEs) (100 mM H(3)PO(4), 50 mM Tris, pH 2.25; 500 mM acetic acid, pH 2.54; 200 mM formi

218 llel quadruplex structure in 22AG-ThT (50 mM Tris, pH 7.2) solution to the antiparallel form just by

219 nd their extension rates determined in 50 mM Tris, pH 8.3, 0.5 mg/ml BSA, 2 mM MgCl(2), and 200 muM e

220 nditions of ionic strength (163 mM) in 50 mM Tris-HCl (pH 7.4) at 37 degrees C.

221 Na(2)S, and 40 microM holo frataxin in 50 mM Tris-HCl (pH 7.5) with 4.3 mM DTT.

222 irpins (and, presumably, duplexes) bind more Tris+ ions than Na+ ions in solution.

223 tides can be modified to the corresponding N-Tris(2, 4,6-trimethoxyphenyl)phosphonium-acetyl (TMPP-Ac

224 after 6.25 h of hybridization in 50 mM NaCl Tris buffer.

225 bovine serum albumin, washing with EDTA/NaCl/Tris buffer, and spraying with inert gases, were used to

226 Upon nonreducing Tris-Tricine-urea-SDS-PAGE, newly synthesized proinsulin

227 ere performed using 2g of sample and 20ml of Tris-HNO3 (pH=8) containing: a) 0.1M NaCl and 2g of skim

228 at pH 8.5 versus the conventional pH 6.8 of Tris-glycine gels.

229 ric DNA, both in the presence and absence of Tris buffer/salt, and sensing the same through its fluor

230 n APP at the mRNA level affect the amount of Tris buffer extractable APP protein and Abeta40 and 42 p

231 coiled DNA can be obscured by Raman bands of Tris counterions.

232 The binding of Tris+, NH4+, Li+, Na+, and K+ to dsDNA was then investig

233 The weak capacity of Tris-borate to stabilize RNA folding may reflect relativ

234 Using various relative concentrations of Tris and either phosphate, tricarballylate (1,2,3-propan

235 red lysis buffer with high concentrations of Tris-HCl and sodium dodecyl sulfate as well as exposure

236 on was between 8.5 and 8.7 with no effect of Tris concentration.

237 However, the effectiveness of Tris-borate as a counterion for RNA has not been systema

238 tudy, we examined the therapeutic effects of Tris DBA on glomerular cell proliferation, renal inflamm

239 The use of volatile buffers instead of Tris-acetate in detection of small molecules by MS impro

240 atic digestions of the substrate in 50 mM of Tris buffer at pH 7.4 generates fluorescence emission at

241 Because the apparent number of Tris+ ions released is greater than that observed by oth

242 red in 90% yields by the Mannich reaction of Tris(hydroxymethyl)phosphine 1 with (l)- or (d)- Alanine

243 On the other hand, the use of Tris-HCl as binding buffer gave higher purification perf

244 tion is a hydrophilic ion like Na+, NH4+, or Tris+ or a hydrophobic ion like tetrabutylammonium.

245 ution buffered to pH 8-8.2 with phosphate or Tris-HCl, followed by reaction with TMPP-acetic acid N-h

246 ning either Tris, acetate, and EDTA (TAE) or Tris, borate, and EDTA (TBE).

247 lted in greater sensitivity than with TBS or Tris.

248 0 min exposure, a fully assembled (mu(3)-oxo)Tris[(mu(2)-peroxo)(mu(2)-glutamato-kappaO:kappaO')](glu

249 ized with tris(hydroxymethyl)aminomethane (P-Tris) was used in affinity membrane chromatography for l

250 c membrane chromatography with three-layer P-Tris nanofiber membranes, the optimal operating conditio

251 findings demonstrated the effectiveness of P-Tris affinity nanofiber membrane for the recovery of lys

252 Langmuir model, the adsorption capacity of P-Tris nanofiber membrane was estimated to be 345.83 mg/g.

253 of hKAT-I and reassesses the effects of pH, Tris, amino acids and alpha-keto acids on the activity o

254 ions for monovalent ions (sodium, potassium, Tris), magnesium ions and commonly used denaturing agent

255 r 2-amino-2-(hydroxymethyl)-1,3-propanediol (Tris base).

256 tage clamp (Day 3), injected CA II protein + Tris or just Tris (Day 3), measured I(NBC) or the initia

257 ssed the utility of the sulfhydryl reductant Tris(2-carboxyethyl)phosphine (TCEP) for both nucleic ac

258 dine hydrochloride (GdnHCl) or the reductant Tris(2-carboxyethyl)phosphine (TCEP) has been analyzed u

259 K, L, and S at neutral pH by high resolution Tris-Tricine SDS-PAGE and matrix-assisted laser desorpti

260 extraction buffers (phosphate buffer saline, Tris-HCl and NaCl) on the extraction efficiency of total

261 Each amphibactin has the same Tris-hydroxamate-containing peptidic headgroup composed

262 freezing without cryoprotection in a simple Tris.HCl buffer containing EGTA (50 mM) and NaCl (50 mM)

263 the effects of magnesium, potassium, sodium, Tris ions, and deoxynucleoside triphosphates on melting

264 e under stirring whereas under non-stirring, Tris buffer at pH 10 with 0.03M (NH4)2SO4 and 30microm M

265 lution of the DNA using a low ionic strength Tris buffer at pH 8.

266 teractions are present in low ionic strength Tris buffers when vimentin is maintained at the "protofi

267 honate and alpha-carboxylate, we synthesized Tris-POC-2-PMPA (21b), which afforded excellent release

268 15-308.15 K without preparation of synthetic Tris seawater buffers.

269 ntration than is possible with standard TAE (Tris/acetate, pH 8.0) or TBE (Tris/borate, pH 8.3) buffe

270 Gaussian-shaped peaks in 20-80 mM TAE (TAE, Tris-acetate-EDTA; Tris, tris[hydroxymethyl]aminomethane

271 form complexes with the borate ions in TBE (Tris-borate-EDTA) buffer, with mobilities that depend on

272 standard TAE (Tris/acetate, pH 8.0) or TBE (Tris/borate, pH 8.3) buffers.

273 Because dpH(i)/dt was greater in CA II than Tris oocytes, and EZA eliminated the difference, injecte

274 The Tris tricine muWestern is completed in an enclosed, stra

275 n ALP was incubated with BCIP for 1 h in the Tris-HCl buffer.

276 sured for two oligomers as a function of the Tris acetate buffer concentration.

277 ept antibody probe plug delivery scheme, the Tris tricine muWestern blot enables 40% higher separatio

278 m alternative reaction pathways available to Tris.

279 times higher using 0.5M NaCl as compared to Tris-HCl and phosphate buffer saline.

280 Because sensitivity to Tris extraction correlates well with nucleotide hydrolys

281 H)(2)(6-Me(3)-TPA)(2)](2+) (1) [6-Me(3)-TPA, Tris(6-methyl-2-pyridylmethyl)amine] with O(2) in CH(2)C

282 Golden trefoils: Tris(alkyne)gold complex [(coct)(3)Au][SbF(6)] (see pict

283 ein solutions (pH 7.4) were reduced by using Tris (2-carboxyethyl) phosphine HCl and irradiated with

284 azidolinker are efficiently removed by using Tris(2-carboxyethyl)phosphine in aqueous solution that i

285 The extract obtained using Tris-HCl/DDT buffer (pH 8) was used in the pre-treatment

286 An extraction procedure using Tris-HCl buffer solution was employed in order to extrac

287 r, EZA had identical effects in CA II versus Tris oocytes.

288 However, when Tris-boric acid-EDTA (TBE, pH 9.1) buffer was used, the

289 PI protein levels positively correlated with Tris-extractable, soluble Abeta40 (p=0.046) and 42 level

290 forms a stable adduct very efficiently with Tris, which protects the abasic site against cleavage.

291 (37.8-46.5%) bound to the column eluted with Tris-HCl buffer, pH 7.5 with a yield up to 76.6%.

292 nsistently more resistant to extraction with Tris.

293 thylene glycol ester of N-formylglycine with Tris(hydroxymethyl)aminomethane, with the rate of peptid

294 and severe lupus nephritis (ASLN) mice with Tris DBA resulted in improved renal function, albuminuri

295 ced by replacement of extracellular Na+ with Tris, by Ni2+ or the Na+/Ca2+ exchanger blocker KB-R7943

296 Replacement of external NaCl with Tris-HCl significantly reduced the magnitude of the GRP-

297 ysis was performed by partial reduction with Tris(2-carboxyethyl)phosphine and real-time mass monitor

298 the oxidized cysteine residues in rSeBP with Tris(2-carboxyethyl)phosphine required addition of a den

299 matin and heme aggregates, sequentially with Tris/SDS buffer and alkaline bicarbonate solution for co

300 ctive media remained largely unchanged, with Tris as the primary cation.