ライフサイエンスコーパス: dodecyl sulfate

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

2 g to anionic phospholipid vesicles or sodium dodecyl sulfate.

3 d with a separation buffer containing sodium dodecyl sulfate.

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

5 esence of the membrane mimetic system sodium dodecyl sulfate.

6 ted and readily extractable from with sodium dodecyl sulfate.

7 fractions that are insoluble in 0.2% sodium dodecyl sulfate.

8 n agar medium and hypersensitivity to sodium dodecyl sulfate.

9 aP cells are selectively sensitive to sodium dodecyl sulfate.

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

11 ldehyde-water with anionic surfactant sodium dodecyl sulfate.

12 trations of ionic surfactants such as sodium dodecyl sulfate.

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

14 nd hypersensitivity to bile salts and sodium dodecyl sulfate.

15 in a 3x standard saline citrate/0.05% sodium dodecyl sulfate/0.001% (3-[(3-cholamidopropyl) dimethyla

16 approximately 0.7% at 25 degrees C), sodium dodecyl sulfate, an ionic detergent, above its CMC ( app

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

18 r-weight complex that is stable in 2% sodium dodecyl sulfate and at temperatures below 65 degrees C,

19 lls, is resistant to dissociation by lithium dodecyl sulfate and behaves as a stable oligomer on lith

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

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

22 le stacking phenomenon in the anionic sodium dodecyl sulfate and sodium cholate micelle systems.

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

24 zed from purified ECM by boiling with sodium dodecyl sulfate and were identified by liquid chromatogr

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

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

27 s most likely due to the formation of sodium dodecyl sulfate- and urea-resistant NEMO dimers through

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

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

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

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

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

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

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

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

36 ous work, a capillary electrophoresis sodium dodecyl sulfate (CE-SDS) method using precolumn labeling

37 lysis using capillary electrophoresis-sodium dodecyl sulfate (CE-SDS) with laser-induced fluorescence

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

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

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

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

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

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

44 Sodium dodecyl sulfate gel electrophoresis detected no proteoly

45 forms of EnvA TM on mildly denaturing sodium dodecyl sulfate gels we identified five conformational s

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

47 e two fractions migrated similarly in sodium dodecyl sulfate gels, the two fractions migrated differe

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

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

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

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

52 Sodium dodecyl sulfate-insoluble Abeta (an indicator of fibrill

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

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

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

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

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

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

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

60 drophobic monomers are solubilized in sodium dodecyl sulfate micelles.

61 Sodium dodecyl sulfate microcapillary gel electrophoresis (SDS

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

63 also found to reduce interference by sodium dodecyl sulfate, Nonidet P-40, or Triton X-100 in the ma

64 exB-TolC complex protected cells from sodium dodecyl sulfate, novobiocin, and ethidium bromide but fa

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

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

67 sted, controls such as nonfluorinated sodium dodecyl sulfate or fluorinated molecules with minimal su

68 phylococcus aureus PGN, repurified by sodium dodecyl sulfate or phenol extraction, activated TLR2 at

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

70 quaternary structures of prestin by lithium dodecyl sulfate-PAGE, perfluoro-octanoate-PAGE, a membra

71 and behaves as a stable oligomer on lithium dodecyl sulfate-PAGE.

72 Methods using sodium dodecyl sulfate poly acrylamide gel electrophoresis and

73 with the receptor density measured by sodium dodecyl sulfate polyacrylamide electrophoresis and autor

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

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

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

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

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

79 from cascaded FF-IEF were analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-

80 A new method for on-chip sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-

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

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

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

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

85 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and i

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

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

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

89 Sodium dodecyl sulfate polyacrylamide gel electrophoresis showe

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

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

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

93 e purified receptor was determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis.

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

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

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

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

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

99 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

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

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

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

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

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

105 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

106 ight chain dimer ("half-antibody") on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

107 ns prior to on-chip protein sizing by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

108 We have performed sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

109 nd alpha 3-integrins were assessed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

110 TR was observable as a 49-kDa band on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

111 change chromatography and preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

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

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

114 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-

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

116 895OR and 43895 using one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis analy

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

118 Two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis analy

119 ovalently bound to the synthase using sodium dodecyl sulfate-polyacrylamide gel electrophoresis analy

120 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analy

121 Careful sodium dodecyl sulfate-polyacrylamide gel electrophoresis analy

122 Modifications were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and 3

123 step of purification were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and d

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

125 and subjected to either separation by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and i

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

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

128 ve virion proteins were identified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and m

129 ined by separation on two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis and m

130 ve polyacrylamide gel electrophoresis/sodium dodecyl sulfate-polyacrylamide gel electrophoresis and m

131 mine-containing LOS by silver-stained sodium dodecyl sulfate-polyacrylamide gel electrophoresis and m

132 tified 60 proteins by two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis and p

133 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and s

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

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

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

137 e obtained by conventional methods of sodium dodecyl sulfate-polyacrylamide gel electrophoresis and W

138 dominant bands (31.7 and 26.1 kDa) in sodium dodecyl sulfate-polyacrylamide gel electrophoresis and W

139 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and w

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

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

142 s of the mutant lipopolysaccharide by sodium dodecyl sulfate-polyacrylamide gel electrophoresis confi

143 n with a molecular mass of 180 kDa on sodium dodecyl sulfate-polyacrylamide gel electrophoresis consi

144 separation of the protein mixtures by sodium dodecyl sulfate-polyacrylamide gel electrophoresis follo

145 xtent of cleavage after separation by sodium dodecyl sulfate-polyacrylamide gel electrophoresis follo

146 veniently coupled to second-dimension sodium dodecyl sulfate-polyacrylamide gel electrophoresis for i

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

148 igest of the protein extracted from a sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel a

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

150 on, the mobility of gH, gB, and gD in sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels

151 negative staining, spectroscopy, and sodium dodecyl sulfate-polyacrylamide gel electrophoresis indic

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

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

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

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

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

157 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of cy

158 s at 144 and 168 kDa, and analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis of LF

159 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of pr

160 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profi

161 transcriptional data, two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis revea

162 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis revea

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

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

165 Vhs translation product comigrated in sodium dodecyl sulfate-polyacrylamide gel electrophoresis with

166 ted, as evidenced by migration during sodium dodecyl sulfate-polyacrylamide gel electrophoresis with

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

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

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

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

171 By using two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis, immu

172 ed to be the same molecular weight on sodium dodecyl sulfate-polyacrylamide gel electrophoresis, whet

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

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

175 ins were separated by one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

176 apsids or with tails were purified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

177 ork, spore extracts were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

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

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

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

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

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

183 ush border proteins that migrate on a sodium-dodecyl sulfate-polyacrylamide gel like a distinct set o

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

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

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

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

188 at results in the formation of large, sodium dodecyl sulfate-resistant complexes involving tight junc

189 , the drug inhibited formation of the sodium dodecyl sulfate-resistant PA oligomer, which occurs in a

190 degrees C in buffer with and without sodium dodecyl sulfate, respectively.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

206 obtained with only anionic surfactant sodium dodecyl sulfate (SDS) as the template.

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

208 cin (DOX) were in-column lysed with a sodium dodecyl sulfate (SDS) containing buffer, their contents

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

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

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

212 Sodium dodecyl sulfate (SDS) facilitates multiwalled carbon nan

213 ative isoelectric focusing (IEF) with sodium dodecyl sulfate (SDS) gel electrophoresis on a polymer m

214 species that migrates as a trimer on sodium dodecyl sulfate (SDS) gel electrophoresis; ATPS promoted

215 Sodium dodecyl sulfate (SDS) has been used as a perturbant to s

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

217 en developed to accurately quantitate sodium dodecyl sulfate (SDS) in aqueous biochemical samples.

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

219 Although the absence of sodium dodecyl sulfate (SDS) in the second-dimension sizing sep

220 tigated the inactivation of prions by sodium dodecyl sulfate (SDS) in weak acid.

221 n-dodecyl-beta-D-maltoside (DDM) and sodium dodecyl sulfate (SDS) is able to suppress analyte adsorp

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

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

224 ach (FCA) was used to calculate water-sodium dodecyl sulfate (SDS) micelle partition coefficients, K(

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

226 pA) transmembrane helices embedded in sodium dodecyl sulfate (SDS) micelles to identify contacts sign

227 self-associates into pentamers within sodium dodecyl sulfate (SDS) micelles, but the oligomeric statu

228 he Abeta(1-40) aggregates produced on sodium dodecyl sulfate (SDS) micelles, which may be a better mo

229 mM NaH2PO4 (pH 7.05) containing 100mM sodium dodecyl sulfate (SDS) mixed with 45% (v/v) methanol to b

230 ompares the rate of denaturation with sodium dodecyl sulfate (SDS) of the individual rungs of protein

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

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

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

234 The treatment of 12-SWNT with sodium dodecyl sulfate (SDS) overcomes this strong nanotube/iso

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

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

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

238 tudent at MIT discovered the power of sodium dodecyl sulfate (SDS) to dissociate the envelope protein

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

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

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

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

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

244 ives, such as benzoic acid, LiCl, and sodium dodecyl sulfate (SDS), on the Wittig reaction has been e

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

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

247 ammonium bromide (CTAB), and anionic, sodium dodecyl sulfate (SDS), surfactants as a function of solu

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

249 and a negatively charged surfactant, sodium dodecyl sulfate (SDS), using capillary electrophoresis (

250 s-EDTA (TE) buffer, PrepMan Ultra, 2% sodium dodecyl sulfate (SDS)-10% Triton X with and without soni

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

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

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

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

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

256 hown by cross-linking and analysis by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis

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

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

259 cent probe, which is copolymerized in sodium dodecyl sulfate (SDS)-polyacrylamide gel.

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

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

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

263 esulting complex of trypsin/fAbeta is sodium dodecyl sulfate (SDS)-stable.

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

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

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

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

268 and killing by the anionic surfactant sodium dodecyl sulfate (SDS).

269 ses, including heat and the detergent sodium dodecyl sulfate (SDS).

270 ntaining denaturing concentrations of sodium dodecyl sulfate (SDS).

271 horesis, even in the presence of 2.5% sodium dodecyl sulfate (SDS).

272 in C in the presence of the detergent sodium dodecyl sulfate (SDS).

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

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

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

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

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

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

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

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

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

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

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

284 in vitro, an increased sensitivity to sodium dodecyl sulfate, suggesting the presence of an additiona

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

286 ere used to fit absorption spectra of sodium dodecyl sulfate suspended HiPco SWNT and CoMoCat SWNT.

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

288 spores are more sensitive to heat and sodium dodecyl sulfate than their wild-type counterparts.

289 hat are more fragile and sensitive to sodium dodecyl sulfate than wild-type biofilms.

290 re sensitive specifically to heat and sodium dodecyl sulfate than wild-type spores, while mspC mutant

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

292 Addition of sodium dodecyl sulfate to the separation buffer (i.e., MEKC) re

293 have expanded naturally in vivo or by sodium dodecyl sulfate treatment in vitro but does not bind to

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

295 The subcomplex is stable in sodium dodecyl sulfate up to 80 degrees C.

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

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

298 In contrast, the presence of sodium dodecyl sulfate was the only factor tested that conclusi

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

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