ライフサイエンスコーパス: electrophoretic

1 Two-dimensional gel electrophoretic analysis corroborated the identity of th

2 Electrophoretic analysis of amplified products demonstra

3 Gel electrophoretic analysis shows that compared to other ri

4 Electrophoretic analysis under reducing conditions showe

5 The electrophoretic analysis was performed in 50 mmol/L NaOH

6 roove binders, UV spectroscopic studies, and electrophoretic analysis were utilized to clarify the bi

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

8 Electrophoretic and chromatographic analyses indicated t

9 titatively measured against well-established electrophoretic and diffusive processes and differ for e

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

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

12 roteomic mass spectrometry, and validated by electrophoretic and histochemical colocalization.

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

14 Protein-based methods, including electrophoretic and immunological techniques, are at tim

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

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

17 tudy to elaborate the interplay of governing electrophoretic and slip-induced/elastic/shear gradient

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

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

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

21 We conducted EM, DNA topology, native electrophoretic assays, and Mg(2+)-dependent self-associ

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

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

24 dialysate was brought to the entrance of the electrophoretic capillary and the coupling consisted in

25 ical size, which are absent from theoretical electrophoretic capture models.

26 The optical and electrophoretic characterization of the analytes before

27 The sample loading and electrophoretic clean-up of biosamples can be done in pa

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

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

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

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

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

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

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

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

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

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

38 ia interfacial solvothermal synthesis or via electrophoretic deposition.

39 The relative standard deviation of the electrophoretic determination is mostly about 5%.

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

41 cteria depended on the relative strengths of electrophoretic drag and electro-osmotic shear forces.

42 effect of laminar flow, Brownian motion and electrophoretic drift, it is shown that the observed tre

43 Here, computational modeling of the electrophoretic drug delivery device is carried out.

44 Electrophoretic drug delivery devices are able to delive

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

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

47 sments are further supported by quantitative electrophoretic experiments of the respective CDNs.

48 The results enable electrophoretic extraction methods to unspecifically pro

49 Hydrodynamic and electrophoretic focusing each appear to affect particle

50 This field gives rise to an electrophoretic force acting directly on a charged subst

51 ributions of the electroosmotic flow and the electrophoretic force on translocation.

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

53 unzipping, all manifestations of an enhanced electrophoretic force.

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

55 .2 were 21 and 9 ms, respectively, at 160 mV electrophoretic force.

56 d by the electroosmotic flow rather than the electrophoretic force.

57 conditions in which electroosmotic flow and electrophoretic forces add or oppose.

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

59 opologically edited DNA molecules, driven by electrophoretic forces, translocate through a narrow ori

60 lation of microbial populations and combines electrophoretic fractionation of bacterial cells with au

61 Capillary electrophoretic glycan analysis was performed on bulk no

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

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

64 Electrophoretic light scattering is typically used to me

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

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

67 S library, or other DNA sample, based on gel-electrophoretic line profiles.

68 Here, we utilize gas-phase electrophoretic macromolecule analysis to show that a Hy

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

70 nt of new and fast gas-phase and in-solution electrophoretic methods coupled to mass spectrometry to

71 Two electrophoretic methods with contactless conductivity de

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

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

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

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

76 The electrophoretic migration operates from the outer perime

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

78 a novel velocity gradient to counterbalance electrophoretic migration.

79 Here, we report on an energy-efficient electrophoretic mixing method capable of nearly eliminat

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

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

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

83 protein adsorption, whatever their apparent electrophoretic mobilities (migration times) are.

84 The electrophoretic mobilities (mu(e)) of the actinides Th a

85 The difference in electrophoretic mobilities between holo- and apo-forms w

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

87 nterflow was varied, analytes with differing electrophoretic mobilities entered the separation channe

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

89 Electrophoretic mobilities of complexes formed by the tw

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

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

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

93 or protein targets requires the knowledge of electrophoretic mobilities of protein-aptamer complexes,

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

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

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

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

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

99 wide range of values are reported for their electrophoretic mobility (EM) measurements.

100 rged species and exhibit large dispersion in electrophoretic mobility (i.e. charge-to-size ratio).

101 empirical models for predicting proteoforms' electrophoretic mobility (mu(ef)) using large-scale top-

102 n capability of CE-MS by employing effective electrophoretic mobility (mu(eff)) as the key parameter

103 electrokinetic (EK) parameters, that is, the electrophoretic mobility (mu(EP)((1))), the particle zet

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

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

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

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

108 ne of the two components of T1 identified by electrophoretic mobility as T1(21).

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

110 ctric field based on the respective particle electrophoretic mobility diameter (EMD) can be achieved

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

112 proaches analyzing the morphology, size, and electrophoretic mobility failed to distinguish between t

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

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

115 er, for the plasma sEVs and plasma mEVs, the electrophoretic mobility increased as the salt concentra

116 Electrophoretic mobility is a basic parameter that descr

117 by size-exclusion chromatography, gas-phase electrophoretic mobility macromolecular analysis, EM, X-

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

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

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

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

122 l mobility analyzer (nES DMA), aka gas-phase electrophoretic mobility molecular analyzer (nES GEMMA),

123 In the case of a so-called nES gas-phase electrophoretic mobility molecular analyzer (nES GEMMA,

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

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

126 over, SOX2/9, but not SOX17, induced altered electrophoretic mobility of ABCC3pr, which was prevented

127 fering with the synthesis of GBF1, alter the electrophoretic mobility of glycoproteins VP7 and NSP4 a

128 typing method that exploits the differential electrophoretic mobility of homoduplex versus heterodupl

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

130 the number N of nucleotides in the aptamer, electrophoretic mobility of N-nucleotide-long ssDNA, and

131 Preliminary investigations demonstrate that electrophoretic mobility of phosphopeptides containing o

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

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

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

135 e protein, which enabled us to show that the electrophoretic mobility of the protein may be tuned thr

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

137 The electrophoretic mobility of the SDS-protein complexes wa

138 eta potential (zeta(P)), the E(EEC), and the electrophoretic mobility of the second kind (mu(EP)((3))

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

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

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

142 rom the HSF1 transcriptional start site, and electrophoretic mobility shift and ChIP assays confirmed

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

144 ved DNA binding motifs were determined using electrophoretic mobility shift and DNase I footprinting

145 Electrophoretic mobility shift and enhancer-blocking ass

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

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

148 analysing activity in in vitro translation, electrophoretic mobility shift and in vitro ribosome pau

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

150 Electrophoretic mobility shift and luciferase reporter a

151 Electrophoretic mobility shift and SEC-MALLS analyses of

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

153 Using electrophoretic mobility shift assay (EMSA) and chromati

154 Using electrophoretic mobility shift assay (EMSA) and isotherm

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

156 2 also regulates the Bdnf gene, we performed electrophoretic mobility shift assay (EMSA), chromatin i

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

158 (ITC), Microscale Thermophoresis (MST), and Electrophoretic Mobility Shift Assay (EMSA).

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

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

161 Electrophoretic mobility shift assay and chromatin immun

162 By electrophoretic mobility shift assay and chromatin immun

163 ing sites at aor promoter were identified by electrophoretic mobility shift assay and DNase I footpri

164 Electrophoretic mobility shift assay and NMR revealed th

165 Chromatin immunoprecipitation and electrophoretic mobility shift assay data revealed that

166 A combination of electrophoretic mobility shift assay experiments and bio

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

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

169 Electrophoretic mobility shift assay showed that OsbZIP4

170 and electrophoretic mobility shift assay shows that RBM24 di

171 Electrophoretic mobility shift assay suggested that the

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

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

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

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

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

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

178 identified by one-hybrid assays in yeast and electrophoretic mobility shift assay.

179 of the site by ExsA was demonstrated via an electrophoretic mobility shift assay.

180 Luciferase reporter and electrophoretic mobility shift assays (EMSA) showed that

181 Electrophoretic mobility shift assays (EMSAs) confirmed

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

183 Like the PTE, electrophoretic mobility shift assays (EMSAs) indicated

184 Electrophoretic mobility shift assays and chromatin immu

185 Results from electrophoretic mobility shift assays and DNA pulldown a

186 bits differential nuclear protein binding in electrophoretic mobility shift assays and drives increas

187 Using electrophoretic mobility shift assays and fluorescence a

188 Electrophoretic mobility shift assays are widely used in

189 Electrophoretic mobility shift assays demonstrated that

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

191 Using electrophoretic mobility shift assays in HeLa cell extra

192 Importantly, electrophoretic mobility shift assays indicated that pur

193 Electrophoretic mobility shift assays provide further ev

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

195 Electrophoretic mobility shift assays revealed that FKPB

196 Electrophoretic mobility shift assays revealed that MtrB

197 Electrophoretic mobility shift assays revealed that RegX

198 Electrophoretic mobility shift assays revealed that Tim

199 Electrophoretic mobility shift assays showed that AaNAC2

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

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

202 Dual luciferase reporter assays and RNA electrophoretic mobility shift assays showed that wild-t

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

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

205 In the current study, we used electrophoretic mobility shift assays to examine the bin

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

207 om gene silencing/overexpression approaches, electrophoretic mobility shift assays, and ChIP revealed

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

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

210 ing, measured by fluorescence anisotropy and electrophoretic mobility shift assays, and our NMR struc

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

212 s by Pol delta in the absence of PCNA, using electrophoretic mobility shift assays, fluorescence inte

213 g purified recombinant Exo1 and nuclease and electrophoretic mobility shift assays, here we determine

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

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

216 Using electrophoretic mobility shift assays, we defined a RegX

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

218 Using electrophoretic mobility shift assays, we observed diffe

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

220 binding to Cdc13 in vitro as demonstrated by electrophoretic mobility shift assays.

221 ativity, forming multiple shifted species in electrophoretic mobility shift assays.

222 nding was corroborated by immunoblotting and electrophoretic mobility shift assays.

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

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

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

226 fluorescent probes, nuclease accessibility, electrophoretic mobility shifts, and blotting.

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

228 ng (for neutrals) of the analyte's effective electrophoretic mobility that caused the analytes to acc

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

230 predicted phenomena of asymptotic, non-zero electrophoretic mobility with increasing ionic strength,

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

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

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

234 NA repair were analyzed by western blotting, electrophoretic mobility-shift assay, and immunohistoche

235 Employing electrophoretic mobility-shift assays, DNA footprinting,

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

237 lowing acidification by light scattering and electrophoretic mobility.

238 gh characteristic mass shifts and changes in electrophoretic mobility.

239 en synthesized by mutant cells had decreased electrophoretic mobility.

240 arge unit, resulting in dramatic decrease in 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 tence of (even low) residual adsorption, the electrophoretic operating conditions (electric field, ca

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

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

248 The electrophoretic pattern of the PK-resistant core of the

249 and LMW glutenins, were identified from the electrophoretic pattern of the protein isolate bioproces

250 matrix via the antiporter, again through an electrophoretic process without cytosol dilution.

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

252 The electrophoretic profile of extracted proteins showed tha

253 a pseudaminic acid derivative, but whose LPS electrophoretic profile was indistinguishable from that

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

255 The electrophoretic profiles of centrifugal ultrafiltration

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

257 hod to obtain characteristic multiwavelength electrophoretic profiles of soluble protein extracts fro

258 shape and motion provide evidence for a self-electrophoretic propulsion mechanism, whereby anodic oxi

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

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

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

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

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

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

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

266 ence microscopy was employed to assess their electrophoretic separation and enrichment.

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

268 Electrophoretic separation and quantification of bound a

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

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

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

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

273 short capillary (5 cm x 15 mum i.d.) for the electrophoretic separation of analytes with an opposing

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

275 seamlessly integrate sample preparation and electrophoretic separation of proteins.

276 nstead of polyacrylamide gel is used for the electrophoretic separation of proteins.

277 from urine, which was followed by an on-chip electrophoretic separation of the concentrated targets f

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

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

280 ophoresis (GEMBE), a robust and miniaturized electrophoretic separation technique, was employed for t

281 Electrophoretic separation was achieved in less than 3.5

282 The same device can be activated to enable electrophoretic separation.

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

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

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

286 Electrophoretic separations conventionally rely on chrom

287 A breadboard approach for electrophoretic separations with contactless conductivit

288 esolution could be improved by the use of an electrophoretic spacer.

289 ed), extraction systems, chromatographic and electrophoretic systems, microfluidic systems (classical

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

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

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

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

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

295 We induce electrophoretic transport by a confined photochemical re

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

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