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 ne (4T1) treated by an antitumor compound, 2-Dodecyl-6-methoxycyclohexa-2, 5-diene-1,4-dione (DMDD),

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

6 nent diblock copolymer melts comprising poly(dodecyl acrylate)-block-poly(lactide).

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

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

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

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

11 tric pai-chromophoric bola-amphiphilic BAB1 (dodecyl and triethyleneglycolmonomethylether containing

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 ensor fabricated from polypyrrole doped with dodecyl benzenesulfonate (PPy (DBS)) is placed over RTN

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

16 Cs of n-octyl beta-d-glucopyranoside (OG), n-dodecyl beta-d-maltopyranoside (DDM), and lauryldimethyl

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

18 llection device as well as the addition of n-Dodecyl beta-d-maltoside (0.01%) in the collection buffe

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

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

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

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

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

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

25 A unique combination of a nonionic detergent dodecyl-beta-d-maltopyranoside (DDM) with urea as protei

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

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

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

29 mosynechococcus elongatus via conventional n-dodecyl-beta-D-maltoside solubilization (DM-PSI) and a,

30 of PSMalpha3 peptides in solution and with n-dodecyl-beta-d-maltoside, a micelle-forming detergent, w

31 solubilization with the nonionic detergent n-dodecyl-beta-d-maltoside, which preserved both hydrophil

32 osphocholine, n-decyl-beta-D-maltoside, or n-dodecyl-beta-D-maltoside.

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

34 hosphatidylcholine can be cosolubilized by n-dodecyl-beta-melibioside to form bicelles.

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

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

37 up based on negatively charged sulfonate and dodecyl chain.

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

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

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

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

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

43 -1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl ester], or the intracellularly applied Ca(2+) ch

44 tential measurements for octaethylene glycol dodecyl ether (C(12)EO(8)), octyl glucoside (OG), and do

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 ther (C(12)EO(8)), octyl glucoside (OG), and dodecyl maltoside.

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

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

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

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

70 upramolecular co-assembly based on lower-rim dodecyl-modified sulfonatocalix[4]arene (SC4AD) and naph

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

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

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

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

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

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

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

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

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

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

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

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

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

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

85 However, BAB2 (dodecyl side chain on both sides) does not show gelation

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

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

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

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

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

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

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

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

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

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

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

97 of n-octanol enhanced with surfactant sodium dodecyl sulfate (SDS) (0.10% in n-octanol) was applied a

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

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

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

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

102 rokinetic chromatography (MEKC) using sodium dodecyl sulfate (SDS) and fused silica capillaries is de

103 ith performance comparable to that of sodium dodecyl sulfate (SDS) and is compatible with mass spectr

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

105 g surfactants: Tween 80, Triton X100, Sodium Dodecyl Sulfate (SDS) and Quillaja Saponin was evaluated

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

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

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

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

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

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

112 Specifically, the intercalation of sodium dodecyl sulfate (SDS) bilayers in a PEM comprising poly(

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

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

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

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

117 Sodium dodecyl sulfate (SDS) facilitates multiwalled carbon nan

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

119 Extensive use of Sodium Dodecyl Sulfate (SDS) in households, agricultural operat

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

121 With stools spiked with sodium dodecyl sulfate (SDS) in situ bacteria lysing and DNA de

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

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

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

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

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

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

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

129 In addition, chemical treatment with sodium dodecyl sulfate (SDS) solutions was tested.

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

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

132 Addition of surfactant (sodium dodecyl sulfate (SDS)), elevation of temperature, additi

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

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

135 n digestion using an ionic detergent, sodium dodecyl sulfate (SDS), at high temperature, conditions w

136 three chemically diverse surfactants, sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (C

137 investigated, including the amount of sodium dodecyl sulfate (SDS), ethanol, and ionic strength in th

138 litensis M28 to the membrane stressor sodium dodecyl sulfate (SDS), indicating cell envelope defects,

139 modelling, and computer simulations, sodium dodecyl sulfate (SDS), over a broad range of concentrati

140 triblock copolymer (L64 or F68), and sodium dodecyl sulfate (SDS), so-called nanoblends, were develo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

156 with homeotropic anchoring induced by sodium dodecyl sulfate (SDS).

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

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

159 n the CMC of commonly used surfactant sodium dodecyl sulfate (SDS).

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

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

162 perfluorohexanesulfonic acid (PFHxS); sodium dodecyl sulfate (SDS); and sodium tetradecyl sulfate (TD

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

164 The addition of sodium dodecyl sulfate (SDS, surfactant), beta-mercaptoethanol

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

166 embled lattice materials (composed of sodium dodecyl sulfate and beta-cyclodextrin) in a spatially re

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

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

169 onfluorinated compounds were identified with dodecyl sulfate and tetradecyl sulfate the most abundant

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

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

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

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

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

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

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

177 otherapeutic proteins were studied in sodium dodecyl sulfate capillary gel electrophoresis (SDS-CGE)

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

179 The level of protein extractable in sodium dodecyl sulfate containing medium under non-reducing con

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

181 ure in an aqueous solution containing sodium dodecyl sulfate in 83% yield.

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

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

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

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

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

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

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

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

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

191 sin or pepsin, and survive boiling in sodium dodecyl sulfate or 5 M guanidine hydrochloride.

192 e thermal cycle number and the use of sodium dodecyl sulfate or PMA enhancer for Gram-negative bacter

193 Methods using sodium dodecyl sulfate poly acrylamide gel electrophoresis and

194 e oil bodies were characterized using sodium dodecyl sulfate polyacrylamide electrophoresis.

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

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

197 Its homogeneity was determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-

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

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

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

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

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

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

204 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and i

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

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

207 Sodium dodecyl sulfate polyacrylamide gel electrophoresis demon

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

209 Sodium dodecyl sulfate polyacrylamide gel electrophoresis showe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

224 r capability to distinguish among PE, sodium dodecyl sulfate, and stearates.

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

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

227 es showed surface tensions lower than sodium dodecyl sulfate, SDS (19.59-36.57 mN/m compared to 38.8

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

229 Sodium dodecyl sulfate, which is commonly applied in microplast

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

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

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

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

234 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

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

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

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

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

239 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

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

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

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

243 The sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

244 By proteomic analysis, using combined sodium dodecyl sulfate-polyacrylamide gel electrophoresis and h

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

246 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and w

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

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

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

250 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profi

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

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

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

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

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

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

257 ldehyde-water with anionic surfactant sodium dodecyl sulfate.

258 trations of ionic surfactants such as sodium dodecyl sulfate.

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

260 nd hypersensitivity to bile salts and sodium dodecyl sulfate.

261 sphate buffer containing 30 mmolL(-1) sodium dodecyl sulfate.

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

263 g to anionic phospholipid vesicles or sodium dodecyl sulfate.

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

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

266 f chemical stripping (incubation with sodium-dodecyl-sulfate (SDS) and beta-mercaptoethanol at 50-60

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

268 Sodium-dodecyl-sulfate poly acrylamide gel electrophoreses (SDS

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

270 It became clear that stearates and sodium dodecyl sulfates can cause substantial overestimation of

271 showed that when the concentration of sodium dodecyl sulfonate (SDS) were lower than critical micelle

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

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

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

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

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

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

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

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

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

281 50 MPa for 0, 2.5 and 5 min) on total sodium dodecyl sulphate (SDS)-soluble and sarcoplasmic proteins

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

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

284 ms in different caprine muscles using sodium dodecyl sulphate glycerol gel electrophoresis (SDS-GGE).

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

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

287 that amyloid-beta, which migrates on sodium dodecyl sulphate polyacrylamide gel electrophoresis with

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

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

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

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

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

293 Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophoresis (SDS

294 ilk showed a noticeable separation on sodium dodecyl sulphate-polyacrylamide gel electrophoresis and

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

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

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

298 crystal structures of LpqN and LpqN bound to dodecyl-trehalose suggest that LpqN directly binds treha

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