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1 ith the same buffer that also contained 25mM sodium dodecyl sulfate.
2 binding to anionic phospholipid vesicles or sodium dodecyl sulfate.
3 ubilized with a separation buffer containing sodium dodecyl sulfate.
4 adoption of alpha-helicity can be induced by sodium dodecyl sulfate.
5 the presence of the membrane mimetic system sodium dodecyl sulfate.
6 associated and readily extractable from with sodium dodecyl sulfate.
7 ellular fractions that are insoluble in 0.2% sodium dodecyl sulfate.
8 efect on agar medium and hypersensitivity to sodium dodecyl sulfate.
9 deltayraP cells are selectively sensitive to sodium dodecyl sulfate.
10 d formaldehyde-water with anionic surfactant sodium dodecyl sulfate.
11 concentrations of ionic surfactants such as sodium dodecyl sulfate.
12 and denaturation by reagents such as urea or sodium dodecyl sulfate.
13 rrier and hypersensitivity to bile salts and sodium dodecyl sulfate.
14 oligo in a 3x standard saline citrate/0.05% sodium dodecyl sulfate/0.001% (3-[(3-cholamidopropyl) di
15 ation ( approximately 0.7% at 25 degrees C), sodium dodecyl sulfate, an ionic detergent, above its CM
16 a denaturing lysis step (in the presence of sodium dodecyl sulfate and alkylating agents that irreve
17 olecular-weight complex that is stable in 2% sodium dodecyl sulfate and at temperatures below 65 degr
18 iched using oppositely charged micelles from sodium dodecyl sulfate and cetyltrimethylammonium bromid
19 on (30 min) and buffer composition (10(-7) % sodium dodecyl sulfate and pH 7.9), a calibration curve
20 e micelle stacking phenomenon in the anionic sodium dodecyl sulfate and sodium cholate micelle system
21 olubilized from purified ECM by boiling with sodium dodecyl sulfate and were identified by liquid chr
22 synthetic wastewater containing surfactant (sodium dodecyl sulfate) and mineral oil, as well as with
23 ed with various surfactants (sodium cholate, sodium dodecyl sulfate, and cetyl trimethylammonium brom
24 This is most likely due to the formation of sodium dodecyl sulfate- and urea-resistant NEMO dimers t
28 fer with high concentrations of Tris-HCl and sodium dodecyl sulfate as well as exposure to high heat.
30 25 ng of total proteins has been realized by sodium dodecyl sulfate capillary gel electrophoresis (SD
31 gG1 using reducing capillary electrophoresis sodium dodecyl sulfate (CE-SDS) and mass spectrometry (M
32 n previous work, a capillary electrophoresis sodium dodecyl sulfate (CE-SDS) method using precolumn l
33 ein analysis using capillary electrophoresis-sodium dodecyl sulfate (CE-SDS) with laser-induced fluor
36 e, doxorubicin, 5'-fluorouracil, forskolin), sodium dodecyl sulfate (+control), and penicillin-G (-co
37 Fos-Cholines, dodecyldimethylglycine, and sodium dodecyl-sulfate denature both RANTES variants at
38 ntained in several different lipid mimetics (sodium dodecyl sulfate, dodecyl phosphocholine, lyso 1-p
40 lyzing forms of EnvA TM on mildly denaturing sodium dodecyl sulfate gels we identified five conformat
42 from the two fractions migrated similarly in sodium dodecyl sulfate gels, the two fractions migrated
43 and lysX were hypersensitive to antibiotics, sodium dodecyl sulfate, heat shock, and reactive oxygen
44 served as model analytes, while humic acid, sodium dodecyl sulfate, hydroxypropyl-beta-cyclodextrin,
45 -walled carbon nanotubes (SWNTs) coated with sodium dodecyl sulfate in microfluidic channels signific
48 lpha-helicity in K2 at low concentrations of sodium dodecyl sulfate is not due to a decrease in the c
49 a beta-sheet conformation in the context of sodium dodecyl sulfate micelles and phospholipid (1:1 1-
50 micellar electrokinetic chromatography using sodium dodecyl sulfate micelles that were electrophoreti
53 n known as K2 in the presence and absence of sodium dodecyl sulfate micelles, and we docked the bound
54 pane] radical initiator, of linoleic acid in sodium dodecyl sulfate micelles, have been determined in
58 ion was also found to reduce interference by sodium dodecyl sulfate, Nonidet P-40, or Triton X-100 in
59 AcrA-MexB-TolC complex protected cells from sodium dodecyl sulfate, novobiocin, and ethidium bromide
60 used a nonreduced capillary electrophoresis-sodium dodecyl sulfate (nrCE-SDS) method for the analysi
62 ants tested, controls such as nonfluorinated sodium dodecyl sulfate or fluorinated molecules with min
63 ble Staphylococcus aureus PGN, repurified by sodium dodecyl sulfate or phenol extraction, activated T
64 t vexAB was induced in the presence of bile, sodium dodecyl sulfate, or novobiocin and that the induc
66 s well with the receptor density measured by sodium dodecyl sulfate polyacrylamide electrophoresis an
70 that have been noted by nonreduced capillary sodium dodecyl sulfate polyacrylamide gel electrophoresi
71 purified to homogeneity and characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresi
72 ctions from cascaded FF-IEF were analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresi
75 labeled with the probe and analyzed by both sodium dodecyl sulfate polyacrylamide gel electrophoresi
76 n of the purified receptor was determined by sodium dodecyl sulfate polyacrylamide gel electrophoresi
78 reduced electrophoretic mobility (shift) in sodium dodecyl sulfate polyacrylamide gel electrophoresi
80 were investigated by 2D isoelectric focusing sodium dodecyl sulfate polyacrylamide gel electrophoresi
81 y high-performance liquid chromatography and sodium dodecyl sulfate polyacrylamide gel electrophoresi
82 oupled plasma mass spectrometry (ICP MS), 1D sodium dodecyl sulfate polyacrylamide gel electrophoresi
83 ionation by centrifugation and separation by sodium dodecyl sulfate polyacrylamide gel electrophoresi
84 tion of the urine by ultracentrifugation and sodium dodecyl sulfate polyacrylamide gel electrophoresi
85 P-treated chloroplast, which is evaluated by sodium dodecyl sulfate polyacrylamide gel electrophoresi
86 ctively immobilizes all sized proteins after sodium dodecyl sulfate polyacrylamide gel electrophoresi
87 quality controls, a biologic binding assay, sodium dodecyl sulfate polyacrylamide gel electrophoresi
88 tric focusing (CIEF) with parallel capillary sodium dodecyl sulfate- polyacrylamide gel electrophores
89 Da were ionized directly from a vacuum-dried sodium dodecyl sulfate-polyacrylamide gel after electrop
90 unodetection in leaf extract was realized by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
91 otease-containing samples into a nonreducing sodium dodecyl sulfate-polyacrylamide gel electrophoresi
95 tability, we used a diagonal two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresi
97 ion separation of alpha- and beta-tubulin by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
100 rotein quantification strategy that involves sodium dodecyl sulfate-polyacrylamide gel electrophoresi
101 in each purified fraction were verified via sodium dodecyl sulfate-polyacrylamide gel electrophoresi
102 yperphosphorylated forms of tau with altered sodium dodecyl sulfate-polyacrylamide gel electrophoresi
103 gically active fractions were resolved using sodium dodecyl sulfate-polyacrylamide gel electrophoresi
104 ains 43895OR and 43895 using one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresi
105 two carbohydrate-containing components with sodium dodecyl sulfate-polyacrylamide gel electrophoresi
106 ysis using an albumin depletion method (with sodium dodecyl sulfate-polyacrylamide gel electrophoresi
107 d proteins were identified as calmodulins by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
108 alyzed by changes in protein migration using sodium dodecyl sulfate-polyacrylamide gel electrophoresi
109 edia were subjected to gel-based separation (sodium dodecyl sulfate-polyacrylamide gel electrophoresi
110 Zta-associated proteins were isolated by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
111 urea-polyacrylamide gel electrophoresis and sodium dodecyl sulfate-polyacrylamide gel electrophoresi
112 739, alter the mobility of Ebola virus NP by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
113 of Cha demonstrated mobility as a trimer on sodium dodecyl sulfate-polyacrylamide gel electrophoresi
114 osylated and accounts for the 58-kDa size by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
115 s His(6)-SQS gave a single band at 42 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
116 ack most extractable coat protein as seen by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
117 The P. ubique enzyme possessed an M(r) on sodium dodecyl sulfate-polyacrylamide gel electrophoresi
119 finity IgG from chronic chagasic sera and on sodium dodecyl sulfate-polyacrylamide gel electrophoresi
120 1R and TRIM5alpha proteins exhibited similar sodium dodecyl sulfate-polyacrylamide gel electrophoresi
122 yptic digest of the protein extracted from a sodium dodecyl sulfate-polyacrylamide gel electrophoresi
123 evidence obtained by conventional methods of sodium dodecyl sulfate-polyacrylamide gel electrophoresi
124 nd identified 60 proteins by two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresi
126 addition, the mobility of gH, gB, and gD in sodium dodecyl sulfate-polyacrylamide gel electrophoresi
129 e proteins were separated by one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresi
130 ilage, separation of the protein mixtures by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
131 Twelve virion proteins were identified by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
132 atus by negative staining, spectroscopy, and sodium dodecyl sulfate-polyacrylamide gel electrophoresi
134 chain-light chain dimer ("half-antibody") on sodium dodecyl sulfate-polyacrylamide gel electrophoresi
135 rimary Vhs translation product comigrated in sodium dodecyl sulfate-polyacrylamide gel electrophoresi
136 t with transcriptional data, two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresi
137 m each step of purification were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
138 proteins prior to on-chip protein sizing by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
140 determined by separation on two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresi
142 two predominant bands (31.7 and 26.1 kDa) in sodium dodecyl sulfate-polyacrylamide gel electrophoresi
143 f the extent of cleavage after separation by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
144 VSH-1 capsids or with tails were purified by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
146 protein with a molecular mass of 180 kDa on sodium dodecyl sulfate-polyacrylamide gel electrophoresi
147 units covalently bound to the synthase using sodium dodecyl sulfate-polyacrylamide gel electrophoresi
148 ta 1- and alpha 3-integrins were assessed by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
152 ue Native polyacrylamide gel electrophoresis/sodium dodecyl sulfate-polyacrylamide gel electrophoresi
154 appeared to be the same molecular weight on sodium dodecyl sulfate-polyacrylamide gel electrophoresi
155 rrent work, spore extracts were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
156 be conveniently coupled to second-dimension sodium dodecyl sulfate-polyacrylamide gel electrophoresi
157 lactosamine-containing LOS by silver-stained sodium dodecyl sulfate-polyacrylamide gel electrophoresi
158 roteins was quantified by performing tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresi
160 nion-exchange chromatography and preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresi
162 Analysis of the mutant lipopolysaccharide by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
163 ration and subjected to either separation by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
164 ycosylated, as evidenced by migration during sodium dodecyl sulfate-polyacrylamide gel electrophoresi
165 ractions at 144 and 168 kDa, and analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
166 Da band corresponding to the DAT detected by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
167 lentil lectin chromatography and preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresi
168 nd their component proteins were resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
169 re marked by a dramatic shift in mobility on sodium dodecyl sulfate-polyacrylamide gel electrophoresi
170 52 kDa, respectively, based on non-reducing sodium dodecyl sulfate-polyacrylamide gel electrophoresi
171 as investigated by immobilized trypsin using sodium dodecyl sulfate-polyacrylamide gel electrophoresi
172 re-function probe through its application in sodium dodecyl sulfate-polyacrylamide gel electrophoresi
173 protein composition, which were confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresi
174 ation with 10% fetal bovine serum; SDS-PAGE, sodium dodecyl sulfate-polyacrylamide gel electrophoresi
175 (3) fragmentation of protein backbones (via sodium dodecyl sulfate-polyacrylamide gel electrophoresi
178 264) were clipped into two portions: one for sodium dodecyl sulfate-polyacrylamide gel electrophoresi
180 he purified rSj97 was >95% pure as judged by sodium dodecyl sulfate-polyacrylamide gel electrophoreti
181 PS, and EPS were also estimated from stained sodium dodecyl sulfate-polyacrylamide gels and verified
185 inal brush border proteins that migrate on a sodium-dodecyl sulfate-polyacrylamide gel like a distinc
186 Western blotting system based on separating sodium-dodecyl sulfate protein complexes by capillary ge
187 tion that results in the formation of large, sodium dodecyl sulfate-resistant complexes involving tig
188 Instead, the drug inhibited formation of the sodium dodecyl sulfate-resistant PA oligomer, which occu
190 th a sodium phosphate buffer containing 2.0% sodium dodecyl sulfate (SDDS) were observed in HMT sampl
191 s then chosen for further comparison against sodium dodecyl sulfate (SDS) (electrostatic), sodium cas
192 n (10 mm I.D. x 160 mm, 10 mum) using 100 mM sodium dodecyl sulfate (SDS) and 1-butanol in 10 mM sodi
193 sis of the protein from leaf flour employing sodium dodecyl sulfate (SDS) and 2-mercaptoethanol (ME)
194 alkylation of proteins in the presence of 1% sodium dodecyl sulfate (SDS) and following with desaltin
198 C 4.2.1.1)--on unfolding upon treatment with sodium dodecyl sulfate (SDS) and refolding upon removal
199 between the straight-chain alkyl surfactant sodium dodecyl sulfate (SDS) and single-walled carbon na
200 was used to probe the micellar structure of sodium dodecyl sulfate (SDS) and sodium cholate (SC) in
201 EC50 ratios for two commercial amphiphiles, sodium dodecyl sulfate (SDS) and Triton X-100, in additi
202 eomic reactor, in which samples dissolved in sodium dodecyl sulfate (SDS) are digested in an ultrafil
205 cellar liquid chromatography (MLC) employing sodium dodecyl sulfate (SDS) as surfactant, were determi
207 into monomers only by treatment with urea or sodium dodecyl sulfate (SDS) but not nonionic detergents
208 oxorubicin (DOX) were in-column lysed with a sodium dodecyl sulfate (SDS) containing buffer, their co
213 at of oligoproline peptides, while detergent sodium dodecyl sulfate (SDS) favors alpha helix in this
214 g non-native isoelectric focusing (IEF) with sodium dodecyl sulfate (SDS) gel electrophoresis on a po
215 rated a species that migrates as a trimer on sodium dodecyl sulfate (SDS) gel electrophoresis; ATPS p
217 ing drug, polyvinylpyrrolidone (PVP) K12 and sodium dodecyl sulfate (SDS) in 1:2.75:0.25 ratio were p
218 has been developed to accurately quantitate sodium dodecyl sulfate (SDS) in aqueous biochemical samp
222 ture of n-dodecyl-beta-D-maltoside (DDM) and sodium dodecyl sulfate (SDS) is able to suppress analyte
225 t approach (FCA) was used to calculate water-sodium dodecyl sulfate (SDS) micelle partition coefficie
227 in A (GpA) transmembrane helices embedded in sodium dodecyl sulfate (SDS) micelles to identify contac
228 PLB self-associates into pentamers within sodium dodecyl sulfate (SDS) micelles, but the oligomeri
229 pared the Abeta(1-40) aggregates produced on sodium dodecyl sulfate (SDS) micelles, which may be a be
230 ous 200mM NaH2PO4 (pH 7.05) containing 100mM sodium dodecyl sulfate (SDS) mixed with 45% (v/v) methan
231 study compares the rate of denaturation with sodium dodecyl sulfate (SDS) of the individual rungs of
232 e-blood samples were treated with 0.1% or 1% sodium dodecyl sulfate (SDS) or 0.1% Triton X-100 and as
233 pseudostationary phase of anionic detergent sodium dodecyl sulfate (SDS) or cationic detergent cetyl
236 e denatured to varying degrees with heat and sodium dodecyl sulfate (SDS) prior to the thermal melt a
237 extraction + in-solution digestion + 2D LC; sodium dodecyl sulfate (SDS) protein extraction + 1D gel
238 Viscosity measurements were obtained for sodium dodecyl sulfate (SDS) solutions, ranging from 1.0
239 duate student at MIT discovered the power of sodium dodecyl sulfate (SDS) to dissociate the envelope
240 ctures (FIOMNs) and mixed hemi/ad-micelle of sodium dodecyl sulfate (SDS) was designed for the magnet
241 between alphaLA and the chemical surfactant sodium dodecyl sulfate (SDS) were also investigated.
242 g paper (DOI 10.1021/bi100338e ), identified sodium dodecyl sulfate (SDS), alone or in combination wi
243 reased sensitivity to lysis by the detergent sodium dodecyl sulfate (SDS), and the vpsC mutant showed
244 ional changes induced by urea, spermine, and sodium dodecyl sulfate (SDS), its interaction with SDS m
245 f additives, such as benzoic acid, LiCl, and sodium dodecyl sulfate (SDS), on the Wittig reaction has
246 anodispersions were prepared using Tween 80, sodium dodecyl sulfate (SDS), sodium caseinate (SC) and
247 an 95% removal of 1-5% detergents, including sodium dodecyl sulfate (SDS), sodium deoxycholate, Chaps
248 imethylammonium bromide (CTAB), and anionic, sodium dodecyl sulfate (SDS), surfactants as a function
249 ated the effects of the chemical denaturants sodium dodecyl sulfate (SDS), urea, guanidine hydrochlor
250 (UBI), and a negatively charged surfactant, sodium dodecyl sulfate (SDS), using capillary electropho
251 ed: Tris-EDTA (TE) buffer, PrepMan Ultra, 2% sodium dodecyl sulfate (SDS)-10% Triton X with and witho
252 f-Acrylamide Clearing Tissue (FACT) is a new sodium dodecyl sulfate (SDS)-based clearing protocol for
254 We report a novel strategy to immobilize sodium dodecyl sulfate (SDS)-coated proteins for fully i
255 er after initial proteolysis with trypsin of sodium dodecyl sulfate (SDS)-extracted I. hospitalis-N.
256 When BSA-SWNT dispersions were subjected to sodium dodecyl sulfate (SDS)-PAGE, BSA passed through th
257 in as shown by cross-linking and analysis by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrop
258 ning temperature gradient focusing (TGF) and sodium dodecyl sulfate (SDS)-polyacrylamide gel electrop
259 developed a rapid, sensitive, and label-free sodium dodecyl sulfate (SDS)-polyacrylamide gel electrop
278 APS, zwitterionic), Triton X-100 (nonionic), sodium dodecyl sulfate (SDS, anionic), and dodecyltrimet
279 ncentration, the ARM absorptivity factor (in sodium dodecyl sulfate [SDS] at 260 nm) of 1.2+/-0.1 (at
280 r glutenin macropolymer particles and varied sodium-dodecyl-sulfate sedimentation volumes, compared w
281 These benefits occurred without changes in sodium dodecyl sulfate-soluble or formic acid-soluble Ab
285 h and, in vitro, an increased sensitivity to sodium dodecyl sulfate, suggesting the presence of an ad
287 hapes were used to fit absorption spectra of sodium dodecyl sulfate suspended HiPco SWNT and CoMoCat
289 these spores are more sensitive to heat and sodium dodecyl sulfate than their wild-type counterparts
291 were more sensitive specifically to heat and sodium dodecyl sulfate than wild-type spores, while mspC
292 r rinsing with buffer solution to remove the sodium dodecyl sulfate, the so-obtained renal ECM scaffo
294 s that have expanded naturally in vivo or by sodium dodecyl sulfate treatment in vitro but does not b
297 .5, containing 8% tetrahydrofurane and 123mM sodium dodecyl sulfate was employed as running buffer.
298 ble immobilization without any modification; sodium dodecyl sulfate was identified to be efficient en
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