ライフサイエンスコーパス: dodecyl

1 ceptional photostability from the 4,6-bis(5'-dodecyl-[2,2'-bithiophene]-5-yl)thieno[3,4-c][1,2,5]thia

2 ) (68)Ge/(68)Ga generator that uses modified dodecyl-3,4,5-trihydroxybenzoate hydrophobically bound t

3 NDH2 has only one known inhibitor, hydroxy-2-dodecyl-4-(1H)-quinolone (HDQ), and this was used along

4 rs of 4-vinylimidazole and copolymers with 1-dodecyl-4-vinylimidazole were used as enzyme mimics to t

5 ture and surface morphologies of poly(2,6-(4-dodecyl-4H-bisthieno[3,2-b:2',3'-d]pyrrole)-random-2,5-(

6 Previously, we have demonstrated that 2-dodecyl-6-methoxycyclohexa-2,5-diene- 1,4-dione (DMDD) r

7 sing the p-channel semiconductor 5,5'-bis-(7-dodecyl-9H-fluoren-2-yl)-2,2'-bithiophene (DDFTTF).

8 medium alkyl chain length (butyl, octyl and dodecyl) added resulted in a better oxidative stability

9 sobutylene-alt-maleic anhydride] and pendant dodecyl alkyl chains, Lucifer Yellow (LY) fluorescent pr

10 We found that an aliphatic (dodecyl) analog of flavin mononucleotide, FC12, leads to

11 All four esters (methyl, hexyl, dodecyl and octadecyl dihydrocaffeates) exhibited relati

12 esence and absence of 100 mg L(-1) of sodium dodecyl benzene sulfonate (SDBS), and Suwannee River Hum

13 Drainage induced by 0.1 mM sodium dodecyl benzene sulfonate, commonly used for A(I) estima

14 that by using the anionic surfactant sodium dodecyl benzenesulfonate (SDBS) in the running buffer th

15 s now been overexpressed, solubilized with n-dodecyl beta- d-maltopyranoside (DDM), and purified to h

16 ermined a precise geometrical model of the n-dodecyl beta-d-maltopyranoside corona surrounding aquapo

17 urified Gt to photoactivated Rho (Rho*) in n-dodecyl beta-D-maltoside (DDM) examined by gel filtratio

18 brane channel (Aquaporin-0) solubilized by n-Dodecyl beta-D-Maltoside and from previously published s

19 Proteins were solubilized using n-dodecyl beta-D-maltoside and separated using SDS-PAGE.

20 membranes were solubilized with 0.1% (w/v) n-dodecyl beta-D-maltoside, and the RC complex was purifie

21 ue native PAGE and FRET assays revealed 1% n-dodecyl beta-d-maltoside-resistant cis-dimerization for

22 the properties of proteomicelles formed by n-dodecyl-beta,D-maltopyranoside (DDM) detergent.

23 or after solubilization and purification in dodecyl-beta-D-maltopyranoside (DDM).

24 om transfected HEK 293 cell membranes with n-dodecyl-beta-D-maltopyranoside.

25 of these, 234 solubilized in the detergent n-dodecyl-beta-D-maltopyranoside.

26 s provided for the ability of the surfactant dodecyl-beta-D-maltoside (DDM) to prevent charge-induced

27 spholiposomes from receptor solubilized in n-dodecyl-beta-d-maltoside analogs.

28 ecting a membrane protein complex within a n-dodecyl-beta-d-maltoside micelle, we demonstrated a powe

29 ific to the interaction with the detergent n-dodecyl-beta-maltoside (beta-DM) or membrane lipids, at

30 Here, we describe the isolation of n-dodecyl-beta-maltoside solubilized, stable, functionally

31 s of unprecedented cavitands based on a meso-dodecyl-calix[4]pyrrole-resorcin[4]arene hybrid scaffold

32 bonds to a beta-cyclodextrin (beta-CD) and a dodecyl chain was achieved with the expectation that the

33 h owes its amphiphilicity to two hydrophobic dodecyl chains on one side of the HTC core and two hydro

34 derivatives tetrasubstituted with hexyl and dodecyl chains show a phase formation that strongly depe

35 is inserted between the thiophene rings and dodecyl chains, and/or 3,4-ethylenedioxy groups are appe

36 Dodecyl creatine ester showed then a 20-fold increase in

37 -oxidative activity was; BHT>octadecyl ester>dodecyl ester>hexyl ester>methyl ester.

38 -1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl ester], or the intracellularly applied Ca(2+) ch

39 he food industry, BHT, alpha-tocopherol, and dodecyl gallate.

40 ckly binds this protocatechuate and then its dodecyl group undergoes a slow interaction with the hydr

41 ure", "racemic by synthesis", n-octyl, and n-dodecyl groups was synthesized.

42 the ones with medium and long chains (octyl, dodecyl, hexadecyl and eicosyl).

43 Using chloroauric acid as precursor and N-dodecyl imidazole as functional monomer, gold nanoroots

44 (HT) ethers (ethyl, butyl, hexyl, octyl and dodecyl) in rat brain slices.

45 well as phenyl iodide, n-hexyl iodide, and n-dodecyl iodide, as electrophiles in model reactions.

46 bition with an IC50 of 0.05 muM, followed by dodecyl (lauryl) protocatechuate with an IC50 of 0.06 mu

47 CR rhodopsin are investigated in micelles of dodecyl maltoside (DDM) and in phospholipid nanodiscs by

48 Using a sugar-based surfactant system of dodecyl maltoside (DDM) in dimethylformamide (DMF), mice

49 In dodecyl maltoside (DDM) micelles, the spectra are well r

50 thylene glycol monododecyl ether (C12E8) and dodecyl maltoside (DDM) protect bovine serum albumin (BS

51 ilization of the functional fold of CB(2) in dodecyl maltoside (DDM)/CHAPS detergent solutions.

52 cle of the protein solubilized in detergent [dodecyl maltoside (DDM)].

53 Dodecyl maltoside (DM)/SDS mixed micelle spheres (0.05-0

54 Solubilizing concentrations of dodecyl maltoside left this decay rate almost unaltered,

55 Thermal denaturation of dodecyl maltoside solubilized CcO proceeds in two consec

56 exclusion chromatography of purified AAC3 in dodecyl maltoside under blue native gel-like conditions

57 length-sensitive cone pigment (VCOP) in 0.1% dodecyl maltoside using fluorescence spectroscopy.

58 of detergents as follows: n-octyl glucoside, dodecyl maltoside, Triton X-100, Tween 20, 3-[(3-cholami

59 of the enzyme solubilized with the detergent dodecyl maltoside, which is visible in electron cryomicr

60 e presence of alkyl sugar detergents such as dodecyl maltoside.

61 dimers can be isolated by gel filtration in dodecyl maltoside.

62 functional stability in Triton X-100 versus dodecyl maltoside.

63 eractions with the isolated transporter in a dodecyl-maltoside detergent environment.

64 fication steps, which include DNA digestion, dodecyl-maltoside detergent extraction, centrifugation,

65 Co-oxidation of dodecyl methyl sulfide occurred efficiently implying tha

66 N,N-dodecyl,methyl-polyethylenimine coatings applied to soli

67 ted erythropoiesis, whereas the LPA2 agonist dodecyl monophosphate (DMP) and the nonlipid specific ag

68 One compound, 4-dodecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide, inh

69 of the particles and of the neat solid of N-dodecyl-N-methyl-3-(pyren-1-yl)propan-1-ammonium chlorid

70 meric emission, the emission from 10(-5) M N-dodecyl-N-methyl-3-(pyren-1-yl)propan-1-ammonium chlorid

71 se of a chiral ammonium bromide, (-)-1R,2S-N-dodecyl-N-methylephedrinium bromide ((-)-DMEBr).

72 We observed the formation of dodecyl oligomers (n </= 4) during the reaction under an

73 lypeptide were identified in the presence of dodecyl phosphocholine detergent micelles.

74 h-resolution structure of huntingtin 1-17 in dodecyl phosphocholine micelles and the topology of its

75 ength TtRp were conducted in the presence of dodecyl phosphocholine micelles to solvate the membrane

76 nza coat protein hemagglutinin HA2, bound to dodecyl phosphocholine micelles, was recently shown to a

77 rent lipid mimetics (sodium dodecyl sulfate, dodecyl phosphocholine, lyso 1-palmitoyl phosphatidylgly

78 proteins, followed by two-dimensional sodium dodecyl polyacrylamide gel electrophoresis identified se

79 fly processed, they are separated via sodium dodecyl-polyacrylamide gel electrophoresis (SDS-PAGE, th

80 ractionation of proteins, followed by sodium dodecyl-polyacrylamide gel electrophoresis.

81 n constant (Ki) was obtained as 0.23 muM but dodecyl protocatechuate is a slow binding inhibitor.

82 In the case of dodecyl protocatechuate, the enzyme quickly binds this p

83 n and carbon NMR analyses that the generated dodecyl radicals lead to the formation of a new thioethe

84 ded), SQ5 and SQ6 (conjugated with hexyl and dodecyl side chain) squaraine derivatives having more te

85 The attached 96 dodecyl side chains provide the solubility of the 25 260

86 -beta-D-Gal-(1 --> 4)-beta-D-GlcNAc-1,2-di-O-dodecyl-sn-glycero (B2NGL) served as model protein-GL co

87 -sheared OTFTs of selenium squaraine bearing dodecyl substituents (denoted as Se-SQ-C12) performed be

88 X-ray powder diffraction revealed that the N-dodecyl-substituted compound was oriented in an intimate

89 rubicin, 5'-fluorouracil, forskolin), sodium dodecyl sulfate (+control), and penicillin-G (-control).

90 ng reducing capillary electrophoresis sodium dodecyl sulfate (CE-SDS) and mass spectrometry (MS).

91 enatured capillary electrophoresis in sodium dodecyl sulfate (CE-SDS).

92 In proteomics, dodecyl sulfate (DS(-)) as sodium salt is commonly used

93 nonreduced capillary electrophoresis-sodium dodecyl sulfate (nrCE-SDS) method for the analysis of di

94 dium phosphate buffer containing 2.0% sodium dodecyl sulfate (SDDS) were observed in HMT samples.

95 chosen for further comparison against sodium dodecyl sulfate (SDS) (electrostatic), sodium caseinate

96 m I.D. x 160 mm, 10 mum) using 100 mM sodium dodecyl sulfate (SDS) and 1-butanol in 10 mM sodium-phos

97 the protein from leaf flour employing sodium dodecyl sulfate (SDS) and 2-mercaptoethanol (ME) resulte

98 ion of proteins in the presence of 1% sodium dodecyl sulfate (SDS) and following with desalting/delip

99 en detected by gel electrophoresis in sodium dodecyl sulfate (SDS) and immunoblotting.

100 The two tested surfactants [anionic sodium dodecyl sulfate (SDS) and nonionic poly(ethylene glycol)

101 An ompH mutant showed sensitivity to sodium dodecyl sulfate (SDS) and polymyxin B and also had a red

102 n the straight-chain alkyl surfactant sodium dodecyl sulfate (SDS) and single-walled carbon nanotubes

103 ed to probe the micellar structure of sodium dodecyl sulfate (SDS) and sodium cholate (SC) in aqueous

104 atios for two commercial amphiphiles, sodium dodecyl sulfate (SDS) and Triton X-100, in addition to a

105 eactor, in which samples dissolved in sodium dodecyl sulfate (SDS) are digested in an ultrafiltration

106 chanically unfolded polyprotein using sodium dodecyl sulfate (SDS) as an example.

107 Using catechin and sodium dodecyl sulfate (SDS) as model molecules, we have shown

108 liquid chromatography (MLC) employing sodium dodecyl sulfate (SDS) as surfactant, were determined.

109 nomers only by treatment with urea or sodium dodecyl sulfate (SDS) but not nonionic detergents.

110 BP underwent either sodium dodecyl sulfate (SDS) decellularization or stepwise, sol

111 The procedure included sodium dodecyl sulfate (SDS) denaturation and chemical reductio

112 The AS sodium dodecyl sulfate (SDS) denatures and unfolds globular pro

113 Sodium dodecyl sulfate (SDS) facilitates multiwalled carbon nan

114 g, polyvinylpyrrolidone (PVP) K12 and sodium dodecyl sulfate (SDS) in 1:2.75:0.25 ratio were produced

115 While the use of sodium dodecyl sulfate (SDS) in separation buffers allows effic

116 Sodium dodecyl sulfate (SDS) is one of the most popular laborat

117 The surfactant sodium dodecyl sulfate (SDS) is widely used as a detergent for

118 s when the hexamer was solubilized by sodium dodecyl sulfate (SDS) micelles in water.

119 samples were treated with 0.1% or 1% sodium dodecyl sulfate (SDS) or 0.1% Triton X-100 and assayed f

120 stationary phase of anionic detergent sodium dodecyl sulfate (SDS) or cationic detergent cetyltrimeth

121 s from immunoblots involve the use of sodium dodecyl sulfate (SDS) or low-pH buffers.

122 ured to varying degrees with heat and sodium dodecyl sulfate (SDS) prior to the thermal melt and acti

123 tion + in-solution digestion + 2D LC; sodium dodecyl sulfate (SDS) protein extraction + 1D gel LC; ph

124 cosity measurements were obtained for sodium dodecyl sulfate (SDS) solutions, ranging from 1.0 to 50.

125 (FIOMNs) and mixed hemi/ad-micelle of sodium dodecyl sulfate (SDS) was designed for the magnetic immo

126 n alphaLA and the chemical surfactant sodium dodecyl sulfate (SDS) were also investigated.

127 (DOI 10.1021/bi100338e ), identified sodium dodecyl sulfate (SDS), alone or in combination with othe

128 sensitivity to lysis by the detergent sodium dodecyl sulfate (SDS), and the vpsC mutant showed minor

129 hanges induced by urea, spermine, and sodium dodecyl sulfate (SDS), its interaction with SDS micelles

130 ersions were prepared using Tween 80, sodium dodecyl sulfate (SDS), sodium caseinate (SC) and SDS-Twe

131 removal of 1-5% detergents, including sodium dodecyl sulfate (SDS), sodium deoxycholate, Chaps, Trito

132 e effects of the chemical denaturants sodium dodecyl sulfate (SDS), urea, guanidine hydrochloride (Gu

133 amide Clearing Tissue (FACT) is a new sodium dodecyl sulfate (SDS)-based clearing protocol for the ch

134 Mixed hemi/ad-micelle sodium dodecyl sulfate (SDS)-coated magnetic iron oxide nanopar

135 report a novel strategy to immobilize sodium dodecyl sulfate (SDS)-coated proteins for fully integrat

136 r initial proteolysis with trypsin of sodium dodecyl sulfate (SDS)-extracted I. hospitalis-N. equitan

137 SA-SWNT dispersions were subjected to sodium dodecyl sulfate (SDS)-PAGE, BSA passed through the stack

138 mperature gradient focusing (TGF) and sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis

139 ed a rapid, sensitive, and label-free sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis

140 and aggregation state, as observed in sodium dodecyl sulfate (SDS)-polyacrylamide gels.

141 In the method, sodium dodecyl sulfate (SDS)-protein complexes are separated by

142 Both PiB binding and the amount of sodium dodecyl sulfate (SDS)-soluble Abeta were able to predict

143 anol and water with the assistance of sodium dodecyl sulfate (SDS).

144 een agarose and SWCNTs suspended with sodium dodecyl sulfate (SDS).

145 (SMCs) were tested with ibuprofen and sodium dodecyl sulfate (SDS).

146 paper, and dye was eluted in 1% (w/v) sodium dodecyl sulfate (SDS).

147 form a ternary complex in presence of sodium dodecyl sulfate (SDS).

148 e solubilized in aqueous solutions of sodium dodecyl sulfate (SDS).

149 a binding partner, the lipid-mimetic sodium dodecyl sulfate (SDS).

150 GF1/IGFBP) complex dissociation using sodium dodecyl sulfate (SDS).

151 itterionic), Triton X-100 (nonionic), sodium dodecyl sulfate (SDS, anionic), and dodecyltrimethylammo

152 tion, the ARM absorptivity factor (in sodium dodecyl sulfate [SDS] at 260 nm) of 1.2+/-0.1 (at 1 SD)

153 turing lysis step (in the presence of sodium dodecyl sulfate and alkylating agents that irreversibly

154 sing oppositely charged micelles from sodium dodecyl sulfate and cetyltrimethylammonium bromide, resp

155 min) and buffer composition (10(-7) % sodium dodecyl sulfate and pH 7.9), a calibration curve of quan

156 sensitive to the detergents deoxycholate and dodecyl sulfate and the antimicrobial peptide polymyxin

157 Using sodium dodecyl sulfate as a membrane model, we examined the NMR

158 Using sodium dodecyl sulfate as a model analyte, quantification was l

159 The addition of sodium dodecyl sulfate as supporting additive further enhanced

160 h high concentrations of Tris-HCl and sodium dodecyl sulfate as well as exposure to high heat.

161 In membranes, dodecyl sulfate blocked chloride transport through the c

162 f total proteins has been realized by sodium dodecyl sulfate capillary gel electrophoresis (SDS CGE)

163 The level of proteins extractable in sodium dodecyl sulfate containing media was fitted using first

164 Using two-dimensional native green/sodium dodecyl sulfate gels, the loosely PSII-bound LHCb was se

165 carbon nanotubes (SWNTs) coated with sodium dodecyl sulfate in microfluidic channels significantly i

166 ures observed for CNTs dispersed with sodium dodecyl sulfate in the absence of DNA.

167 licity in K2 at low concentrations of sodium dodecyl sulfate is not due to a decrease in the critical

168 -sheet conformation in the context of sodium dodecyl sulfate micelles and phospholipid (1:1 1-palmito

169 r electrokinetic chromatography using sodium dodecyl sulfate micelles that were electrophoretically i

170 The overall linker placement in sodium dodecyl sulfate micelles was identified by NMR experimen

171 Using membrane-mimicking sodium dodecyl sulfate micelles, an NMR derived structural mode

172 as K2 in the presence and absence of sodium dodecyl sulfate micelles, and we docked the bound struct

173 adical initiator, of linoleic acid in sodium dodecyl sulfate micelles, have been determined in terms

174 Preferential adsorption of sodium dodecyl sulfate on {111} planes of Cu(2)O crystals, whic

175 Methods using sodium dodecyl sulfate poly acrylamide gel electrophoresis and

176 vestigated by 2D isoelectric focusing sodium dodecyl sulfate polyacrylamide gel electrophoresis (IEF/

177 plasma mass spectrometry (ICP MS), 1D sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS

178 immobilizes all sized proteins after sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-

179 d electrophoretic mobility (shift) in sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-

180 The use of sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-

181 The assay comprises non-reducing sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-

182 d to homogeneity and characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-

183 ed chloroplast, which is evaluated by sodium dodecyl sulfate polyacrylamide gel electrophoresis and c

184 d with the probe and analyzed by both sodium dodecyl sulfate polyacrylamide gel electrophoresis and i

185 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and i

186 alysis of the human plaque tissues by sodium dodecyl sulfate polyacrylamide gel electrophoresis confi

187 the urine by ultracentrifugation and sodium dodecyl sulfate polyacrylamide gel electrophoresis demon

188 entrifugal fractionation coupled with sodium dodecyl sulfate polyacrylamide gel electrophoresis mobil

189 Sodium dodecyl sulfate polyacrylamide gel electrophoresis showe

190 n by centrifugation and separation by sodium dodecyl sulfate polyacrylamide gel electrophoresis, foll

191 y controls, a biologic binding assay, sodium dodecyl sulfate polyacrylamide gel electrophoresis, mass

192 ve been noted by nonreduced capillary sodium dodecyl sulfate polyacrylamide gel electrophoresis, reve

193 performance liquid chromatography and sodium dodecyl sulfate polyacrylamide gel electrophoresis.

194 n blotting system based on separating sodium-dodecyl sulfate protein complexes by capillary gel elect

195 nor corneas and decellularized with a sodium dodecyl sulfate solution.

196 The sodium dodecyl sulfate stability of the two proteins was consis

197 re sensitive to acid, bile salts, and sodium dodecyl sulfate stresses.

198 he well-known, commercially available sodium dodecyl sulfate surfactant media.

199 While addition of electrolyte to sodium dodecyl sulfate suspensions of single-wall carbon nanotu

200 taining 8% tetrahydrofurane and 123mM sodium dodecyl sulfate was employed as running buffer.

201 obilization without any modification; sodium dodecyl sulfate was identified to be efficient enough fo

202 icellar systems consisting of anionic sodium dodecyl sulfate with explicit solvent.

203 tic wastewater containing surfactant (sodium dodecyl sulfate) and mineral oil, as well as with shale

204 onq = 5,8-dioxydo-1,4-naphtoquinonato, DOS = dodecyl sulfate) with pyrenyl-functionalized poly(aryles

205 various surfactants (sodium cholate, sodium dodecyl sulfate, and cetyl trimethylammonium bromide).

206 in several different lipid mimetics (sodium dodecyl sulfate, dodecyl phosphocholine, lyso 1-palmitoy

207 X were hypersensitive to antibiotics, sodium dodecyl sulfate, heat shock, and reactive oxygen and nit

208 as model analytes, while humic acid, sodium dodecyl sulfate, hydroxypropyl-beta-cyclodextrin, and Na

209 An aqueous mixture of CuCl(2), sodium dodecyl sulfate, NaOH, and NH(2)OH.HCl was prepared to p

210 was induced in the presence of bile, sodium dodecyl sulfate, or novobiocin and that the induction of

211 ng with buffer solution to remove the sodium dodecyl sulfate, the so-obtained renal ECM scaffolds wer

212 cusing (CIEF) with parallel capillary sodium dodecyl sulfate- polyacrylamide gel electrophoresis (SDS

213 cellularized with distilled water and sodium dodecyl sulfate-based solution.

214 composition, which were confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

215 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

216 re clipped into two portions: one for sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

217 containing samples into a nonreducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

218 A modified Laemmli sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

219 In addition, when sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

220 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

221 aration of alpha- and beta-tubulin by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

222 Analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

223 quantification strategy that involves sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

224 h purified fraction were verified via sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

225 ing an albumin depletion method (with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

226 stigated by immobilized trypsin using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

227 895OR and 43895 using one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis analy

228 Two-dimensional blue native-sodium dodecyl sulfate-polyacrylamide gel electrophoresis analy

229 -associated proteins were isolated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and i

230 ins were identified as calmodulins by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and l

231 )-SQS gave a single band at 42 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and m

232 was quantified by performing tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis and s

233 demonstrated mobility as a trimer on sodium dodecyl sulfate-polyacrylamide gel electrophoresis and t

234 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and w

235 by changes in protein migration using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and W

236 tion probe through its application in sodium dodecyl sulfate-polyacrylamide gel electrophoresis assay

237 ter the mobility of Ebola virus NP by sodium dodecyl sulfate-polyacrylamide gel electrophoresis by 5

238 Proteins were separated on a sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel a

239 IgG from chronic chagasic sera and on sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels

240 y, we used a diagonal two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis metho

241 sphorylated forms of tau with altered sodium dodecyl sulfate-polyacrylamide gel electrophoresis migra

242 rbohydrate-containing components with sodium dodecyl sulfate-polyacrylamide gel electrophoresis mobil

243 TRIM5alpha proteins exhibited similar sodium dodecyl sulfate-polyacrylamide gel electrophoresis mobil

244 P. ubique enzyme possessed an M(r) on sodium dodecyl sulfate-polyacrylamide gel electrophoresis of 38

245 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profi

246 ction in leaf extract was realized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis SDS-P

247 olyacrylamide gel electrophoresis and sodium dodecyl sulfate-polyacrylamide gel electrophoresis Weste

248 re subjected to gel-based separation (sodium dodecyl sulfate-polyacrylamide gel electrophoresis) and

249 agmentation of protein backbones (via sodium dodecyl sulfate-polyacrylamide gel electrophoresis).

250 t extractable coat protein as seen by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, as w

251 Samples were resolved using sodium dodecyl sulfate-polyacrylamide gel electrophoresis, foll

252 active fractions were resolved using sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

253 d and accounts for the 58-kDa size by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

254 , respectively, based on non-reducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

255 roMMP processing was determined using sodium dodecyl sulfate-polyacrylamide gel electrophoresis/N-ter

256 ith 10% fetal bovine serum; SDS-PAGE, sodium dodecyl sulfate-polyacrylamide gel electrophoresis; RANK

257 Results of 16S rRNA gene sequencing, sodium dodecyl sulfate-polyacrylamide gel electrophoretic analy

258 fied rSj97 was >95% pure as judged by sodium dodecyl sulfate-polyacrylamide gel electrophoretic analy

259 EPS were also estimated from stained sodium dodecyl sulfate-polyacrylamide gels and verified by West

260 lysis of two-dimensional blue native/lithium dodecyl sulfate-polyacrylamide gels indicated that no in

261 igrated at the mobility of U(S)1.5 in sodium dodecyl sulfate-polyacrylamide gels.

262 benefits occurred without changes in sodium dodecyl sulfate-soluble or formic acid-soluble Abeta poo

263 trations of ionic surfactants such as sodium dodecyl sulfate.

264 aturation by reagents such as urea or sodium dodecyl sulfate.

265 nd hypersensitivity to bile salts and sodium dodecyl sulfate.

266 same buffer that also contained 25mM sodium dodecyl sulfate.

267 g to anionic phospholipid vesicles or sodium dodecyl sulfate.

268 d with a separation buffer containing sodium dodecyl sulfate.

269 n of alpha-helicity can be induced by sodium dodecyl sulfate.

270 e turned off through addition of the blocker dodecyl sulfate.

271 ldehyde-water with anionic surfactant sodium dodecyl sulfate.

272 aws, and decellularized by successive sodium dodecyl sulfate/Triton-X cycles.

273 Cholines, dodecyldimethylglycine, and sodium dodecyl-sulfate denature both RANTES variants at low pH,

274 nin macropolymer particles and varied sodium-dodecyl-sulfate sedimentation volumes, compared with tho

275 B with Se(IV) ions in the presence of sodium dodecyl sulphate (SDS) and Ponpe 7.5.

276 ormation between the ionic surfactant sodium dodecyl sulphate (SDS) and the phenolic acid salicylic a

277 Sodium dodecyl sulphate (SDS) enhanced PPO activity, with pulp

278 The electrokinetic injection of sodium dodecyl sulphate (SDS) including sample (-10 kV, 20 s) w

279 this work, the stabilising effect of sodium dodecyl sulphate (SDS) micelles on pH-induced colour var

280 f emulsifiers, lecithin, Tween-20 and sodium dodecyl sulphate (SDS) were tested.

281 be improved by adding a cosurfactant (sodium dodecyl sulphate (SDS)).

282 -gel method using anionic surfactant, sodium dodecyl sulphate (SDS), as template to control the size

283 B) in acid medium, in the presence of sodium dodecyl sulphate (SDS), producing a yellow compound (lam

284 50 MPa for 0, 2.5 and 5 min) on total sodium dodecyl sulphate (SDS)-soluble and sarcoplasmic proteins

285 EGCG) oxidation (400muM) in Tween- or sodium dodecyl sulphate (SDS)-stabilised hexadecane emulsions.

286 osphate buffer at pH 7.0 and 30 mM of sodium dodecyl sulphate at an applied voltage of 25 kV.

287 racted proteins were characterised by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS

288 a soluble fraction was carried out by sodium dodecyl sulphate polyacrylamide gel electrophoresis afte

289 gation of Fab to HRG was confirmed by sodium dodecyl sulphate polyacrylamide gel electrophoresis-West

290 um by addition of lithium acetate and Sodium dodecyl sulphate, followed by centrifugation and alcohol

291 lar weight of 23 kDa as determined by sodium dodecyl sulphate-polyaccrylamide gel electrophoresis (SD

292 s in adulterated samples by utilising sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS

293 py, atomic force microscopy (AFM) and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS

294 e liquid chromatography (SE-HPLC) and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS

295 Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophoresis (SDS

296 r mass of approximately 25 kDa on 12% sodium dodecyl sulphate-polyacrylamide gel electrophoresis.

297 ynapses by apolipoprotein E4 includes sodium dodecyl sulphate-stable dimers and trimers.

298 Proteins were denatured by sodium dodecyl-sulphate (SDS) and precipitated as potassium sal

299 on for analytes with high polarities such as dodecyl trimethylammonium bromide and bradykinin are est

300 ion was focused using a cationic surfactant (dodecyl trimethylammonium bromide, DTAB) solution in a m