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1 trations of ionic surfactants such as sodium dodecyl sulfate.
2 aturation by reagents such as urea or sodium dodecyl sulfate.
3 nd hypersensitivity to bile salts and sodium dodecyl sulfate.
4 sphate buffer containing 30 mmolL(-1) sodium dodecyl sulfate.
5 same buffer that also contained 25mM sodium dodecyl sulfate.
6 g to anionic phospholipid vesicles or sodium dodecyl sulfate.
7 d with a separation buffer containing sodium dodecyl sulfate.
8 n of alpha-helicity can be induced by sodium dodecyl sulfate.
9 esence of the membrane mimetic system sodium dodecyl sulfate.
10 ted and readily extractable from with sodium dodecyl sulfate.
11 fractions that are insoluble in 0.2% sodium dodecyl sulfate.
12 e turned off through addition of the blocker dodecyl sulfate.
13 ldehyde-water with anionic surfactant sodium dodecyl sulfate.
14 in a 3x standard saline citrate/0.05% sodium dodecyl sulfate/0.001% (3-[(3-cholamidopropyl) dimethyla
15 turing lysis step (in the presence of sodium dodecyl sulfate and alkylating agents that irreversibly
16 lls, is resistant to dissociation by lithium dodecyl sulfate and behaves as a stable oligomer on lith
17 embled lattice materials (composed of sodium dodecyl sulfate and beta-cyclodextrin) in a spatially re
18 sing oppositely charged micelles from sodium dodecyl sulfate and cetyltrimethylammonium bromide, resp
19 min) and buffer composition (10(-7) % sodium dodecyl sulfate and pH 7.9), a calibration curve of quan
21 onfluorinated compounds were identified with dodecyl sulfate and tetradecyl sulfate the most abundant
22 sensitive to the detergents deoxycholate and dodecyl sulfate and the antimicrobial peptide polymyxin
23 zed from purified ECM by boiling with sodium dodecyl sulfate and were identified by liquid chromatogr
24 tic wastewater containing surfactant (sodium dodecyl sulfate) and mineral oil, as well as with shale
25 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
34 It became clear that stearates and sodium dodecyl sulfates can cause substantial overestimation of
35 f total proteins has been realized by sodium dodecyl sulfate capillary gel electrophoresis (SDS CGE)
36 otherapeutic proteins were studied in sodium dodecyl sulfate capillary gel electrophoresis (SDS-CGE)
37 ng reducing capillary electrophoresis sodium dodecyl sulfate (CE-SDS) and mass spectrometry (MS).
38 ous work, a capillary electrophoresis sodium dodecyl sulfate (CE-SDS) method using precolumn labeling
39 lysis using capillary electrophoresis-sodium dodecyl sulfate (CE-SDS) with laser-induced fluorescence
41 The level of proteins extractable in sodium dodecyl sulfate containing media was fitted using first
42 The level of protein extractable in sodium dodecyl sulfate containing medium under non-reducing con
43 rubicin, 5'-fluorouracil, forskolin), sodium dodecyl sulfate (+control), and penicillin-G (-control).
44 Cholines, dodecyldimethylglycine, and sodium dodecyl-sulfate denature both RANTES variants at low pH,
45 in several different lipid mimetics (sodium dodecyl sulfate, dodecyl phosphocholine, lyso 1-palmitoy
47 Using two-dimensional native green/sodium dodecyl sulfate gels, the loosely PSII-bound LHCb was se
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
51 carbon nanotubes (SWNTs) coated with sodium dodecyl sulfate in microfluidic channels significantly i
54 licity in K2 at low concentrations of sodium dodecyl sulfate is not due to a decrease in the critical
55 -sheet conformation in the context of sodium dodecyl sulfate micelles and phospholipid (1:1 1-palmito
56 r electrokinetic chromatography using sodium dodecyl sulfate micelles that were electrophoretically i
59 as K2 in the presence and absence of sodium dodecyl sulfate micelles, and we docked the bound struct
60 adical initiator, of linoleic acid in sodium dodecyl sulfate micelles, have been determined in terms
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
68 sted, controls such as nonfluorinated sodium dodecyl sulfate or fluorinated molecules with minimal su
69 phylococcus aureus PGN, repurified by sodium dodecyl sulfate or phenol extraction, activated TLR2 at
70 e thermal cycle number and the use of sodium dodecyl sulfate or PMA enhancer for Gram-negative bacter
71 was induced in the presence of bile, sodium dodecyl sulfate, or novobiocin and that the induction of
72 quaternary structures of prestin by lithium dodecyl sulfate-PAGE, perfluoro-octanoate-PAGE, a membra
76 with the receptor density measured by sodium dodecyl sulfate polyacrylamide electrophoresis and autor
78 vestigated by 2D isoelectric focusing sodium dodecyl sulfate polyacrylamide gel electrophoresis (IEF/
79 plasma mass spectrometry (ICP MS), 1D sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS
80 immobilizes all sized proteins after sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-
83 d to homogeneity and characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-
84 from cascaded FF-IEF were analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-
85 d electrophoretic mobility (shift) in sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-
86 Its homogeneity was determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-
87 ed chloroplast, which is evaluated by sodium dodecyl sulfate polyacrylamide gel electrophoresis and c
89 d with the probe and analyzed by both sodium dodecyl sulfate polyacrylamide gel electrophoresis and i
90 alysis of the human plaque tissues by sodium dodecyl sulfate polyacrylamide gel electrophoresis confi
91 the urine by ultracentrifugation and sodium dodecyl sulfate polyacrylamide gel electrophoresis demon
93 entrifugal fractionation coupled with sodium dodecyl sulfate polyacrylamide gel electrophoresis mobil
95 n by centrifugation and separation by sodium dodecyl sulfate polyacrylamide gel electrophoresis, foll
96 y controls, a biologic binding assay, sodium dodecyl sulfate polyacrylamide gel electrophoresis, mass
97 ve been noted by nonreduced capillary sodium dodecyl sulfate polyacrylamide gel electrophoresis, reve
100 cusing (CIEF) with parallel capillary sodium dodecyl sulfate- polyacrylamide gel electrophoresis (SDS
101 composition, which were confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
103 re clipped into two portions: one for sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
104 containing samples into a nonreducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
108 aration of alpha- and beta-tubulin by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
110 quantification strategy that involves sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
111 h purified fraction were verified via sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
112 ing an albumin depletion method (with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
114 ight chain dimer ("half-antibody") on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
115 ns prior to on-chip protein sizing by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
117 nd alpha 3-integrins were assessed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
119 stigated by immobilized trypsin using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-
120 895OR and 43895 using one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis analy
123 ovalently bound to the synthase using sodium dodecyl sulfate-polyacrylamide gel electrophoresis analy
124 step of purification were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and d
125 By proteomic analysis, using combined sodium dodecyl sulfate-polyacrylamide gel electrophoresis and h
126 -associated proteins were isolated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and i
127 ins were identified as calmodulins by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and l
128 )-SQS gave a single band at 42 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and m
129 ve virion proteins were identified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and m
130 ined by separation on two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis and m
131 tified 60 proteins by two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis and p
132 was quantified by performing tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis and s
133 demonstrated mobility as a trimer on sodium dodecyl sulfate-polyacrylamide gel electrophoresis and t
135 by changes in protein migration using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and W
136 e obtained by conventional methods of sodium dodecyl sulfate-polyacrylamide gel electrophoresis and W
137 dominant bands (31.7 and 26.1 kDa) in sodium dodecyl sulfate-polyacrylamide gel electrophoresis and W
138 tion probe through its application in sodium dodecyl sulfate-polyacrylamide gel electrophoresis assay
139 ter the mobility of Ebola virus NP by sodium dodecyl sulfate-polyacrylamide gel electrophoresis by 5
140 n with a molecular mass of 180 kDa on sodium dodecyl sulfate-polyacrylamide gel electrophoresis consi
141 separation of the protein mixtures by sodium dodecyl sulfate-polyacrylamide gel electrophoresis follo
142 xtent of cleavage after separation by sodium dodecyl sulfate-polyacrylamide gel electrophoresis follo
144 igest of the protein extracted from a sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel a
145 IgG from chronic chagasic sera and on sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels
146 on, the mobility of gH, gB, and gD in sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels
147 negative staining, spectroscopy, and sodium dodecyl sulfate-polyacrylamide gel electrophoresis indic
148 y, we used a diagonal two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis metho
149 sphorylated forms of tau with altered sodium dodecyl sulfate-polyacrylamide gel electrophoresis migra
150 rbohydrate-containing components with sodium dodecyl sulfate-polyacrylamide gel electrophoresis mobil
151 TRIM5alpha proteins exhibited similar sodium dodecyl sulfate-polyacrylamide gel electrophoresis mobil
152 P. ubique enzyme possessed an M(r) on sodium dodecyl sulfate-polyacrylamide gel electrophoresis of 38
156 transcriptional data, two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis revea
158 ction in leaf extract was realized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis SDS-P
159 olyacrylamide gel electrophoresis and sodium dodecyl sulfate-polyacrylamide gel electrophoresis Weste
160 Vhs translation product comigrated in sodium dodecyl sulfate-polyacrylamide gel electrophoresis with
161 re subjected to gel-based separation (sodium dodecyl sulfate-polyacrylamide gel electrophoresis) and
162 agmentation of protein backbones (via sodium dodecyl sulfate-polyacrylamide gel electrophoresis).
163 t extractable coat protein as seen by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, as w
167 d and accounts for the 58-kDa size by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.
168 ins were separated by one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis.
169 apsids or with tails were purified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.
170 , respectively, based on non-reducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis.
171 roMMP processing was determined using sodium dodecyl sulfate-polyacrylamide gel electrophoresis/N-ter
172 ith 10% fetal bovine serum; SDS-PAGE, sodium dodecyl sulfate-polyacrylamide gel electrophoresis; RANK
173 Results of 16S rRNA gene sequencing, sodium dodecyl sulfate-polyacrylamide gel electrophoretic analy
174 fied rSj97 was >95% pure as judged by sodium dodecyl sulfate-polyacrylamide gel electrophoretic analy
175 EPS were also estimated from stained sodium dodecyl sulfate-polyacrylamide gels and verified by West
176 lysis of two-dimensional blue native/lithium dodecyl sulfate-polyacrylamide gels indicated that no in
178 n blotting system based on separating sodium-dodecyl sulfate protein complexes by capillary gel elect
179 , the drug inhibited formation of the sodium dodecyl sulfate-resistant PA oligomer, which occurs in a
180 dium phosphate buffer containing 2.0% sodium dodecyl sulfate (SDDS) were observed in HMT samples.
181 of n-octanol enhanced with surfactant sodium dodecyl sulfate (SDS) (0.10% in n-octanol) was applied a
182 chosen for further comparison against sodium dodecyl sulfate (SDS) (electrostatic), sodium caseinate
183 m I.D. x 160 mm, 10 mum) using 100 mM sodium dodecyl sulfate (SDS) and 1-butanol in 10 mM sodium-phos
184 the protein from leaf flour employing sodium dodecyl sulfate (SDS) and 2-mercaptoethanol (ME) resulte
185 ion of proteins in the presence of 1% sodium dodecyl sulfate (SDS) and following with desalting/delip
186 rokinetic chromatography (MEKC) using sodium dodecyl sulfate (SDS) and fused silica capillaries is de
188 ith performance comparable to that of sodium dodecyl sulfate (SDS) and is compatible with mass spectr
189 The two tested surfactants [anionic sodium dodecyl sulfate (SDS) and nonionic poly(ethylene glycol)
190 An ompH mutant showed sensitivity to sodium dodecyl sulfate (SDS) and polymyxin B and also had a red
191 g surfactants: Tween 80, Triton X100, Sodium Dodecyl Sulfate (SDS) and Quillaja Saponin was evaluated
192 n the straight-chain alkyl surfactant sodium dodecyl sulfate (SDS) and single-walled carbon nanotubes
193 ed to probe the micellar structure of sodium dodecyl sulfate (SDS) and sodium cholate (SC) in aqueous
194 atios for two commercial amphiphiles, sodium dodecyl sulfate (SDS) and Triton X-100, in addition to a
195 eactor, in which samples dissolved in sodium dodecyl sulfate (SDS) are digested in an ultrafiltration
198 liquid chromatography (MLC) employing sodium dodecyl sulfate (SDS) as surfactant, were determined.
200 Specifically, the intercalation of sodium dodecyl sulfate (SDS) bilayers in a PEM comprising poly(
206 species that migrates as a trimer on sodium dodecyl sulfate (SDS) gel electrophoresis; ATPS promoted
208 g, polyvinylpyrrolidone (PVP) K12 and sodium dodecyl sulfate (SDS) in 1:2.75:0.25 ratio were produced
214 n-dodecyl-beta-D-maltoside (DDM) and sodium dodecyl sulfate (SDS) is able to suppress analyte adsorp
218 he Abeta(1-40) aggregates produced on sodium dodecyl sulfate (SDS) micelles, which may be a better mo
219 mM NaH2PO4 (pH 7.05) containing 100mM sodium dodecyl sulfate (SDS) mixed with 45% (v/v) methanol to b
220 ompares the rate of denaturation with sodium dodecyl sulfate (SDS) of the individual rungs of protein
221 samples were treated with 0.1% or 1% sodium dodecyl sulfate (SDS) or 0.1% Triton X-100 and assayed f
222 stationary phase of anionic detergent sodium dodecyl sulfate (SDS) or cationic detergent cetyltrimeth
225 ured to varying degrees with heat and sodium dodecyl sulfate (SDS) prior to the thermal melt and acti
226 tion + in-solution digestion + 2D LC; sodium dodecyl sulfate (SDS) protein extraction + 1D gel LC; ph
228 cosity measurements were obtained for sodium dodecyl sulfate (SDS) solutions, ranging from 1.0 to 50.
229 tudent at MIT discovered the power of sodium dodecyl sulfate (SDS) to dissociate the envelope protein
230 (FIOMNs) and mixed hemi/ad-micelle of sodium dodecyl sulfate (SDS) was designed for the magnetic immo
233 (DOI 10.1021/bi100338e ), identified sodium dodecyl sulfate (SDS), alone or in combination with othe
234 sensitivity to lysis by the detergent sodium dodecyl sulfate (SDS), and the vpsC mutant showed minor
235 n digestion using an ionic detergent, sodium dodecyl sulfate (SDS), at high temperature, conditions w
236 three chemically diverse surfactants, sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (C
237 investigated, including the amount of sodium dodecyl sulfate (SDS), ethanol, and ionic strength in th
238 litensis M28 to the membrane stressor sodium dodecyl sulfate (SDS), indicating cell envelope defects,
239 hanges induced by urea, spermine, and sodium dodecyl sulfate (SDS), its interaction with SDS micelles
240 ives, such as benzoic acid, LiCl, and sodium dodecyl sulfate (SDS), on the Wittig reaction has been e
241 modelling, and computer simulations, sodium dodecyl sulfate (SDS), over a broad range of concentrati
242 triblock copolymer (L64 or F68), and sodium dodecyl sulfate (SDS), so-called nanoblends, were develo
243 ersions were prepared using Tween 80, sodium dodecyl sulfate (SDS), sodium caseinate (SC) and SDS-Twe
244 removal of 1-5% detergents, including sodium dodecyl sulfate (SDS), sodium deoxycholate, Chaps, Trito
245 ammonium bromide (CTAB), and anionic, sodium dodecyl sulfate (SDS), surfactants as a function of solu
246 e effects of the chemical denaturants sodium dodecyl sulfate (SDS), urea, guanidine hydrochloride (Gu
247 and a negatively charged surfactant, sodium dodecyl sulfate (SDS), using capillary electrophoresis (
248 amide Clearing Tissue (FACT) is a new sodium dodecyl sulfate (SDS)-based clearing protocol for the ch
250 report a novel strategy to immobilize sodium dodecyl sulfate (SDS)-coated proteins for fully integrat
251 r initial proteolysis with trypsin of sodium dodecyl sulfate (SDS)-extracted I. hospitalis-N. equitan
252 SA-SWNT dispersions were subjected to sodium dodecyl sulfate (SDS)-PAGE, BSA passed through the stack
253 hown by cross-linking and analysis by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis
254 mperature gradient focusing (TGF) and sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis
255 ed a rapid, sensitive, and label-free sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis
258 Both PiB binding and the amount of sodium dodecyl sulfate (SDS)-soluble Abeta were able to predict
273 perfluorohexanesulfonic acid (PFHxS); sodium dodecyl sulfate (SDS); and sodium tetradecyl sulfate (TD
274 itterionic), Triton X-100 (nonionic), sodium dodecyl sulfate (SDS, anionic), and dodecyltrimethylammo
276 f chemical stripping (incubation with sodium-dodecyl-sulfate (SDS) and beta-mercaptoethanol at 50-60
277 tion, the ARM absorptivity factor (in sodium dodecyl sulfate [SDS] at 260 nm) of 1.2+/-0.1 (at 1 SD)
278 es showed surface tensions lower than sodium dodecyl sulfate, SDS (19.59-36.57 mN/m compared to 38.8
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
284 in vitro, an increased sensitivity to sodium dodecyl sulfate, suggesting the presence of an additiona
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
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 have expanded naturally in vivo or by sodium dodecyl sulfate treatment in vitro but does not bind to
296 obilization without any modification; sodium dodecyl sulfate was identified to be efficient enough fo
300 onq = 5,8-dioxydo-1,4-naphtoquinonato, DOS = dodecyl sulfate) with pyrenyl-functionalized poly(aryles