ライフサイエンスコーパス: electrophoretic

1 Purified MBH contains all 14 subunits by electrophoretic analysis (13 subunits were also identifi

2 al data were generated by means of gel-based electrophoretic analysis and nanoliquid chromatography/h

3 Electrophoretic analysis of amplified products demonstra

4 e method with BCG was evident in bioanalyzer electrophoretic analysis of isolated RNA, which revealed

5 based on their physical characteristics and electrophoretic analysis of the polypeptides associated

6 Gel electrophoretic analysis shows that compared to other ri

7 ysine bound permanently to RG-II, precluding electrophoretic analysis.

8 Electrophoretic and chromatographic analyses indicated t

9 Membrane proteins, responding to electrophoretic and electroosmotic forces, have long bee

10 tes are concentrated near the IDZ when their electrophoretic and electroosmotic velocities balance.

11 n of human gamma-tubulins according to their electrophoretic and immunochemical properties.

12 of the separation and direct correlation of electrophoretic and MALDI-MS results.

13 ctuating hydrodynamics approach recovers the electrophoretic and relaxation corrections obtained by D

14 (SKJ, Katsuwonus pelamis) - were compared by electrophoretic and western blot analyses to identify bi

15 different buffers and separated by different electrophoretic approaches [native, urea, acid urea PAGE

16 We present an on-chip electrophoretic assay for rapid protein detection with a

17 ] repeats in the LPA gene) and a serum-based electrophoretic assay in patients and controls (frequenc

18 Here we report on the unexpected electrophoretic behavior of complexes between rod-like v

19 l imidazolium tetrafluoroborate (bminBF4) as electrophoretic buffer solution.

20 th the Ca(2+) ionophore ETH129, which allows electrophoretic Ca(2+) uptake, isolated yeast mitochondr

21 nferred permeability transition sensitive to electrophoretic Ca(2+) uptake.

22 The optical and electrophoretic characterization of the analytes before

23 the device and weaved into straight channel electrophoretic chips in a single step.

24 assessed by endogenous damage markers and by electrophoretic "comet" measurements.

25 an age of 41 years (range: 19-54 years) with electrophoretic confirmation of sickle cell disease were

26 opose that injection with nanopipettes using electrophoretic delivery is an excellent alternative whe

27 und-evoked activity was achieved through the electrophoretic delivery of calcium indicators.

28 ls into an electric current, which regulates electrophoretic delivery of chemical substances without

29 Electrophoretic deposition (EPD) is used to assemble met

30 Here we describe size-dependent electrophoretic deposition (EPD) of citrate-stabilized A

31 les on stainless steel substrates during the electrophoretic deposition (EPD) process.

32 d for the functionalization of nHfO2@RGO and electrophoretic deposition (EPD) technique was used for

33 niques, electrochemical deposition (ECD) and electrophoretic deposition (EPD), in enzyme immobilizati

34 Our preliminary results show that an electrophoretic deposition can be applied to produce hig

35 talum were coated with a layer of (100)Mo by electrophoretic deposition followed by high-temperature

36 The electrophoretic deposition of Mn3O4 nanoparticles (15-20

37 The throwing power of the electrophoretic deposition technique, a method suitable

38 as layer-by-layer deposition, self-assembly, electrophoretic deposition, hydrogel casting, doctor bla

39 The electrophoretic determination indicated a macromolecular

40 We present an origami paper-based electrophoretic device (oPAD-Ep) that achieves rapid ( a

41 n of target-binding oligonucleotides, and an electrophoretic DNA manipulation scheme for the coupling

42 cribe a new method for neuronal labelling by electrophoretic dye delivery from a suction electrode di

43 Second, each graphene acts as an electrophoretic electrode for site-specific probe DNA im

44 The focusing position of streptavidin in electrophoretic-electroosmotic focusing (EEF) experiment

45 sses of protein out of the open microfluidic electrophoretic (EP) cytometry device.

46 The results enable electrophoretic extraction methods to unspecifically pro

47 thus cannot be explained by the reversal of electrophoretic flows of Ca2+.

48 Hydrodynamic and electrophoretic focusing each appear to affect particle

49 We leverage isotachophoresis (ITP), an electrophoretic focusing technique, to create a stationa

50 uctuations can be achieved by increasing the electrophoretic force used in nanopore sequencing device

51 a-hemolysin (alpha-HL) protein pore under an electrophoretic force.

52 .2 were 21 and 9 ms, respectively, at 160 mV electrophoretic force.

53 unzipping, all manifestations of an enhanced electrophoretic force.

54 ection of cells with a nanopipette and using electrophoretic forces for the delivery of molecules.

55 ngth distributions are calculated to predict electrophoretic gel banding patterns.

56 icum aestivum) has been purified to apparent electrophoretic homogeneity with a final specific activi

57 amplification reaction for detection and gel electrophoretic identification of human Immunodeficiency

58 NEP delivery bypassed endocytosis by electrophoretic injection of nanoparticles into human br

59 Electrophoretic introduction of antibody into and along

60 llary electrophoresis instruments as well as electrophoretic lab-on-chip devices, while maintaining a

61 Electrophoretic light scattering is typically used to me

62 microscopy and spectroscopy, and dynamic and electrophoretic light scattering, we characterized the i

63 th a zeta potential of -35.5mV determined by electrophoretic light scattering.

64 backs: for example, it is put to good use in electrophoretic mass determinations but limits enzyme ef

65 performs the PCR amplification and microchip electrophoretic (ME) separation for rapid forensic short

66 nd asparagine by a simple and fast capillary electrophoretic method.

67 Two electrophoretic methods with contactless conductivity de

68 We used glycan TMT-labeling to improve electrophoretic migration and enable multiplexed quantit

69 acted from different tissues showed abnormal electrophoretic migration and low melting temperature.

70 We report for the first time how electrophoretic migration of ions and charged nanopartic

71 applied to understand the structure specific electrophoretic migration of the different sugar molecul

72 the untreated one (control), showed a higher electrophoretic migration of the major albumin fraction

73 s is transferred by diffusion alone and with electrophoretic migration.

74 rmalized approach curve is unaffected by the electrophoretic migration.

75 the stationary fixed zone using in-capillary electrophoretic mixing.

76 to differ biochemically and to be part of an electrophoretic mixture compared to high-prevalence vari

77 hs, the T = 3 and T = 4 capsids had the same electrophoretic mobilities (7.4 x 10(-5) cm(2) V(-1) s(-

78 Electrophoretic mobilities and particle sizes of individ

79 approach, we obtain absolute values for the electrophoretic mobilities characterizing solvated prote

80 in good agreement with values predicted from electrophoretic mobilities measured for their minus ends

81 Electrophoretic mobilities of complexes formed by the tw

82 We compared (i) electrophoretic mobilities of known N-glycans from well-

83 by the virions and antibodies migrated with electrophoretic mobilities of much greater absolute valu

84 proteins through standard addition, (ii) the electrophoretic mobilities of N-glycans with their molec

85 , KCE methods require accurate prediction of electrophoretic mobilities of protein-ligand complexes.

86 resis (CE) was used for determination of the electrophoretic mobilities of the liposomes and for dete

87 n-DNA complex with experimentally determined electrophoretic mobilities of the protein and DNA.

88 Effective electrophoretic mobilities of these compounds were deter

89 of dispersity based on the distributions of electrophoretic mobilities was derived and the heterogen

90 single-charged particles according to their electrophoretic mobility (EM) diameter after transition

91 It allows for measuring electrophoretic mobility (mu) as a function of size.

92 2) were activated and MLK3 exhibited reduced electrophoretic mobility (shift) in sodium dodecyl sulfa

93 to DNA was also observed as a change to DNA electrophoretic mobility and a decreased ability to inte

94 lfhydryl content, protein fractions, protein electrophoretic mobility and immunoreactivity) was inves

95 Correlations of NP aggregation rates with electrophoretic mobility and the molecular weight distri

96 d PHL1 factors to P1BS was confirmed by Y1H, electrophoretic mobility assay and chromatin immunopreci

97 ividual mitochondrial membrane potential and electrophoretic mobility by capillary electrophoresis wi

98 MP2, from Pompe iPSC-CMs demonstrated higher electrophoretic mobility compared with control iPSC-CMs.

99 acromolecular analyzer (GEMMA) for analyzing electrophoretic mobility diameters of isolated TBE virio

100 tion of membrane potential and comparison of electrophoretic mobility distributions in preparations c

101 quence-specific model for predicting peptide electrophoretic mobility has been developed using large-

102 tification as the aggregates have negligible electrophoretic mobility in the gel and the isolated nan

103 Electrophoretic mobility is a basic parameter that descr

104 Electrophoretic mobility is a heterogeneous surface prop

105 vaccine particle fractionation and gas-phase electrophoretic mobility macromolecular analyzer (GEMMA)

106 Electrophoretic mobility measurements revealed a signifi

107 oparticles and quartz sand were evaluated by electrophoretic mobility measurements.

108 molecule in the membrane was estimated from electrophoretic mobility measurements.

109 Gas-phase electrophoretic mobility molecular analysis (GEMMA) sepa

110 rs either the diffusion coefficient D or the electrophoretic mobility mu.

111 ytical output parameter for this device, the electrophoretic mobility of a sedimentation marker, Naph

112 omyocytes using SICM and then determined the electrophoretic mobility of isoproterenol in a high ion

113 formation of tRNAHis, as suggested by slower electrophoretic mobility of mutated tRNA with respect to

114 activity of KFEE is defined by the relative electrophoretic mobility of oxLDL, the fragmentation of

115 The theory links the unknown electrophoretic mobility of protein-DNA complex with exp

116 showed that addition of GIPCs decreased the electrophoretic mobility of radiolabelled RG-II, suggest

117 2D-DiGE revealed that the electrophoretic mobility of several discrete protein spo

118 cal approach for an accurate estimate of the electrophoretic mobility of such complexes.

119 within five cysteine pairs and increased the electrophoretic mobility of the corresponding mutants.

120 e exclusively sensitive to PNGase F, and the electrophoretic mobility of the protein was substantiall

121 such selection but require the knowledge of electrophoretic mobility of the protein-ligand complex.

122 gions of interest, we observed dependence of electrophoretic mobility on membrane potential, with pol

123 mutagenesis revealed that the differences in electrophoretic mobility originate in the C-terminal reg

124 of a natural soluble form of CL-12 having an electrophoretic mobility pattern close to that of shed s

125 A), our method is based on the design of low electrophoretic mobility PNA probes, which do not focus

126 lle to solvent stacking mechanism (effective electrophoretic mobility reversal) working at high conce

127 Electrophoretic mobility shift (EMSA) and chromatin immu

128 Furthermore, we show, using electrophoretic mobility shift and chromatin immunopreci

129 Complexes 3a-c interacted with DNA in electrophoretic mobility shift and ethidium bromide bind

130 ed its DNA binding properties in vitro using electrophoretic mobility shift and fluorescence anisotro

131 rphisms were characterized in vitro by using electrophoretic mobility shift and luciferase activity a

132 Electrophoretic mobility shift and luciferase reporter a

133 Electrophoretic mobility shift and SEC-MALLS analyses of

134 These values were confirmed by electrophoretic mobility shift assay (EMSA) analysis, wh

135 Here, we use electrophoretic mobility shift assay (EMSA) and atomic f

136 Using electrophoretic mobility shift assay (EMSA) and chromati

137 Using electrophoretic mobility shift assay (EMSA) and isotherm

138 We performed electrophoretic mobility shift assay (EMSA) using wild-t

139 2 also regulates the Bdnf gene, we performed electrophoretic mobility shift assay (EMSA), chromatin i

140 to viral terminal repeat DNA as assessed by electrophoretic mobility shift assay (EMSA), the mutatio

141 ctor such as U2AF65, as determined by an RNA electrophoretic mobility shift assay and a chromatin imm

142 the snRNA duplex during di-snRNP assembly by electrophoretic mobility shift assay and accompanying co

143 By electrophoretic mobility shift assay and chromatin immun

144 lement in the AOC1 promoter was confirmed by electrophoretic mobility shift assay and chromatin immun

145 Electrophoretic mobility shift assay and chromatin immun

146 SNP function was evaluated by electrophoretic mobility shift assay and promoter lucife

147 Chromatin immunoprecipitation and electrophoretic mobility shift assay data revealed that

148 A combination of electrophoretic mobility shift assay experiments and bio

149 Electrophoretic mobility shift assay gel shift patterns

150 Electrophoretic mobility shift assay indicated that P-Rh

151 appaB-luciferase reporter into cell lines or electrophoretic mobility shift assay of lysate.

152 Electrophoretic mobility shift assay results demonstrate

153 re also up-regulated in resistant plants and electrophoretic mobility shift assay revealed sequence-s

154 An electrophoretic mobility shift assay showed that Arn pre

155 Electrophoretic mobility shift assay showed that OsbZIP4

156 We showed by electrophoretic mobility shift assay that the C terminus

157 ht mass spectrometry of a band excised after electrophoretic mobility shift assay using a ZTRE probe.

158 f detecting nuclear transcription factors by electrophoretic mobility shift assay using digoxigenin (

159 rcular dichroism, NMR, microcalorimetry, and electrophoretic mobility shift assay), we have character

160 AR RNA interaction using UV melting studies, electrophoretic mobility shift assay, and RNase A footpr

161 ding motifs were investigated by competitive electrophoretic mobility shift assay, which revealed tha

162 Activation of GATA3 was analysed by electrophoretic mobility shift assay.

163 he optimal N/P ratio was 50 as determined by electrophoretic mobility shift assay.

164 d with nonmethylated G or A alleles in a gel electrophoretic mobility shift assay.

165 Using recombinant ArsR in electrophoretic mobility shift assays (EMSA), we localiz

166 Electrophoretic mobility shift assays (EMSAs) confirmed

167 We describe a platform for high-throughput electrophoretic mobility shift assays (EMSAs) for identi

168 es and target antigen, we introduce affinity electrophoretic mobility shift assays (EMSAs) in a high-

169 Electrophoretic mobility shift assays (EMSAs) revealed t

170 Western blot analysis and electrophoretic mobility shift assays (EMSAs) showed tha

171 transcription factor binding was analyzed by electrophoretic mobility shift assays (EMSAs) with Jurka

172 etween nmoA and nmoR, which was confirmed by electrophoretic mobility shift assays (EMSAs) with the p

173 as hexahistidine fusion proteins, and using electrophoretic mobility shift assays (EMSAs), the IHFal

174 RNA electrophoretic mobility shift assays (RNA-EMSA) were us

175 Using electrophoretic mobility shift assays and fluorescence a

176 of these genes by VqsM has been confirmed by electrophoretic mobility shift assays and quantitative r

177 Electrophoretic mobility shift assays demonstrate that c

178 tivation experiments, mutation analyses, and electrophoretic mobility shift assays demonstrate that t

179 Electrophoretic mobility shift assays demonstrated decre

180 Electrophoretic mobility shift assays demonstrated that

181 Electrophoretic mobility shift assays demonstrated that

182 , deletion studies, mutagenesis studies, and electrophoretic mobility shift assays identified a PPARa

183 e lead SNP rs4888378; multiplexed competitor electrophoretic mobility shift assays implicated FOXA as

184 Using electrophoretic mobility shift assays in HeLa cell extra

185 Electrophoretic mobility shift assays on the shortlist d

186 Electrophoretic mobility shift assays provide further ev

187 se to DNAm changes upon modulation of HOTAIR Electrophoretic mobility shift assays provided further e

188 Electrophoretic mobility shift assays revealed a direct

189 Electrophoretic mobility shift assays revealed that FKPB

190 Electrophoretic mobility shift assays revealed that RegX

191 Electrophoretic mobility shift assays revealed that Tim

192 Electrophoretic mobility shift assays showed that AaNAC2

193 A bacterial one-hybrid system technique and electrophoretic mobility shift assays showed that AioR i

194 Chromatin-Immunoprecipitation-qPCR and electrophoretic mobility shift assays showed that MdMYB8

195 r of AAO3 in mesophyll cell protoplasts, and electrophoretic mobility shift assays showed that NAP ca

196 We also show through electrophoretic mobility shift assays that OsARID3 speci

197 We demonstrate using electrophoretic mobility shift assays that Rv0678 binds

198 We used deep sequencing and electrophoretic mobility shift assays to derive in vitro

199 Surface plasmon resonance diffraction and electrophoretic mobility shift assays were consistent wi

200 In silico analysis and electrophoretic mobility shift assays were used to asses

201 veral transcription factor-binding sites and electrophoretic mobility shift assays with MCF-7 nuclear

202 izing cell-based luciferase reporter assays, electrophoretic mobility shift assays, and chromatin imm

203 Bacterial one-hybrid screening, electrophoretic mobility shift assays, and coimmunopreci

204 The WRKY70 binding site was defined using electrophoretic mobility shift assays, and its importanc

205 Quantitative chromatin immunoprecipitation, electrophoretic mobility shift assays, and luciferase re

206 Using saturation mutagenesis, electrophoretic mobility shift assays, and RNA-sequencin

207 shown by ChIP-assays, bind KLF16 in vivo In electrophoretic mobility shift assays, KLF16 binds speci

208 In combination with mutational analysis and electrophoretic mobility shift assays, our results provi

209 Electrophoretic mobility shift assays, quantitative reve

210 In electrophoretic mobility shift assays, the purified rPG2

211 In addition to electrophoretic mobility shift assays, this model was co

212 From the results of in vitro translation and electrophoretic mobility shift assays, we demonstrate th

213 Using fluorescence polarization and electrophoretic mobility shift assays, we demonstrate th

214 Using electrophoretic mobility shift assays, we observed diffe

215 ormed a more stable complex with Bdnf RNA in electrophoretic mobility shift assays.

216 to the cydAB promoter DNA was analyzed using electrophoretic mobility shift assays.

217 scription factor binding was investigated by electrophoretic mobility shift assays.

218 nt using flow cytometry, transactivation and electrophoretic mobility shift assays.

219 Using fluorescence anisotropy and electrophoretic mobility shift binding assays, we have d

220 Optimized electrophoretic mobility shift conditions allowed for 10

221 terminus prevented ability of CK1 to induce electrophoretic mobility shift of Dvl3 and its even subc

222 nstants of 5.03 muM, (ii) a Ca(2+)-dependent electrophoretic mobility shift, and (iii) a marked Ca(2+

223 e structural change of Pah1, as reflected by electrophoretic mobility shift, occurs through its phosp

224 tophosphorylation-dependent DBT turnover and electrophoretic mobility shifts in S2 cells.

225 e DBT (DBT(WT)), and neither exhibited daily electrophoretic mobility shifts, suggesting that DBT aut

226 omain, one in the serine cluster that causes electrophoretic mobility upshift and the other outside t

227 Cross-linked complexes are separated by electrophoretic mobility using free solution CE or by si

228 For most trypsinogen variants, shifts in electrophoretic mobility were observed upon raising the

229 ividual mitochondrial membrane potential and electrophoretic mobility were observed.

230 ension and exhibits little change in size or electrophoretic mobility with changing ionic strength (I

231 ed a linear relationship with their relative electrophoretic mobility, and size information on unknow

232 ss, M) are the two major factors determining electrophoretic mobility, in complete agreement with pre

233 Here, we report gel electrophoretic mobility, sucrose gradient sedimentation

234 the net overall surface charge-and thus the electrophoretic mobility-of the ampholyte sums to zero.

235 analyzed for DNA binding with the use of an electrophoretic mobility-shift assay (EMSA) and confocal

236 lowing acidification by light scattering and electrophoretic mobility.

237 gh characteristic mass shifts and changes in electrophoretic mobility.

238 en synthesized by mutant cells had decreased electrophoretic mobility.

239 zed regions of interest displaying decreased electrophoretic mobility.

240 re were revealed by a slight increase in DNA electrophoretic mobility.

241 ropensity tend to have higher than predicted electrophoretic mobility; the incorporation of these fea

242 Luciferase reporter and electrophoretic-mobility shift assay for the FUT6 varian

243 However electrophoretic nucleic acid extraction from bacteria ha

244 With a rapid and simple actuation protocol electrophoretic nucleic acid extraction is easy automata

245 of fluorescent signals without the need for electrophoretic or complex instrumentations, preservatio

246 qualitative and quantitative changes in the electrophoretic pattern of proteins were also observed;

247 Electrophoretic patterns and HPLC chromatograms of the p

248 In this paper, we describe a fabric-based electrophoretic platform for protein separation.

249 he released GFP, were integrated in a single electrophoretic process.

250 le linearly with voltage, consistent with an electrophoretic process.

251 One of the reasons is that electrophoretic processing of unfragmented genomic DNA s

252 reutzfeldt-Jakob disease and had the typical electrophoretic profile associated with this disease.

253 The electrophoretic profile of extracted proteins showed tha

254 The electrophoretic profile showed that BSG is mainly compos

255 o evaluated for total amino acid content and electrophoretic profile, showing a suitable amount of es

256 ar weights determined by MALDI-MS, and (iii) electrophoretic profiles of N-glycans enzymatically trea

257 There were no differences in the electrophoretic profiles of the jelly samples when the p

258 protein diffusion on cellulose membranes and electrophoretic protein profiles were assessed.

259 ed by SDS-PAGE, showing differences in their electrophoretic protein profiles.

260 The in-house fabricated microchips, electrophoretic protocols, and solution matrixes were ke

261 al activation of voltage-gated channels, and electrophoretic redistribution of membrane components.

262 As the aim is to conserve electrophoretic resolution and complete compatibility wi

263 correspond to F(ab')2 variants with average electrophoretic resolution of 1.05.

264 three peaks correspond to Fc/2 variants with electrophoretic resolution up to 2.10, and the last thre

265 otein assay that combines the selectivity of electrophoretic separation and immunoassay.

266 Electrophoretic separation and quantification of bound a

267 The parameters that have an influence on the electrophoretic separation and the MSPE process were stu

268 luidic devices with a 23 cm long, serpentine electrophoretic separation channel and integrated nanoel

269 a QuEChERS extraction procedure followed by electrophoretic separation in NH4HCO3 electrolyte (adjus

270 d measurement system with derivatization and electrophoretic separation integrated on a single microc

271 verage, but has lower throughput because the electrophoretic separation is relatively slow.

272 allel into the separation channels, allowing electrophoretic separation of biomolecules in the drople

273 emical detection on this microchip, where an electrophoretic separation of dopamine and catechol and

274 seamlessly integrate sample preparation and electrophoretic separation of proteins.

275 w capillary temperature required for quality electrophoretic separation of the hybrids from excess pr

276 actor that contributes to band broadening in electrophoretic separation systems in capillaries and mi

277 other functional BER assays with no need of electrophoretic separation, straightforward, easy and re

278 maintaining the electrical connection during electrophoretic separation.

279 e ionic strength of the sample impairing the electrophoretic separation.

280 single run (<3 min/sample) where multiplexed electrophoretic separations are coupled to high resoluti

281 length (15 cm to the UV detector) fast 20 s electrophoretic separations can be obtained.

282 ass microfluidic devices designed to perform electrophoretic separations of cationic species.

283 a are needed to better design and understand electrophoretic separations of subpopulations of mitocho

284 A breadboard approach for electrophoretic separations with contactless conductivit

285 the electrically insulating material allows electrophoretic separations.

286 The code can efficiently handle complex electrophoretic setups coupling sharp electric field gra

287 g the induction of AhR expression by LPS and electrophoretic shift assays demonstrated that this NF-k

288 mparing these results with those obtained by electrophoretic technique such as SDS-PAGE.

289 IMS is a gas-phase electrophoretic technique that enables the separation of

290 l chemical cross-linking with several common electrophoretic techniques to measure the stoichiometry

291 ntation methods can be used in tandem on the electrophoretic time scale for improved protein characte

292 ysis, the process of finding each band in an electrophoretic trace and mapping it to a position in th

293 We induce electrophoretic transport by a confined photochemical re

294 Nanopore sensing involves an electrophoretic transport of analytes through a nanoscal

295 sized dendritic polyelectrolyte that enables electrophoretic transport of aromatic substances.

296 horesis-based bioanlaytical assays, in which electrophoretic transport, separation, or focusing contr

297 nitude slower than expected for conventional electrophoretic transport.

298 e research program that found similarly high electrophoretic variability in many different species an

299 d on the reversal of the analytes' effective electrophoretic velocities at a dynamic stacking boundar

300 After electrophoretic washing, the fluorophore-labeled DNA str