ライフサイエンスコーパス: polyacrylamide gel

1 roteins or peptides inside a surfactant-free polyacrylamide gel.

2 microwells located in a approximately 40 mum polyacrylamide gel.

3 le (blue light) and photoreactive (UV light) polyacrylamide gel.

4 tep after dehydrating the antigen-containing polyacrylamide gel.

5 ng a photoactive benzophenone methacrylamide polyacrylamide gel.

6 xes that were readily detected on denaturing polyacrylamide gels.

7 nately as a monomer and dimer on blue native polyacrylamide gels.

8 ng properties compared to existing ultrathin polyacrylamide gels.

9 hod to detect the oxidation of methionine on polyacrylamide gels.

10 fixing methylene blue bands in nucleic acid polyacrylamide gels.

11 as observed in sodium dodecyl sulfate (SDS)-polyacrylamide gels.

12 uct was obtained that was homogeneous on SDS-polyacrylamide gels.

13 obility of U(S)1.5 in sodium dodecyl sulfate-polyacrylamide gels.

14 r fractionation of proteins in 4% to 20% SDS-polyacrylamide gels.

15 , alginate gels, and fibrin gels, but not in polyacrylamide gels.

16 or application in both aqueous solutions and polyacrylamide gels.

17 In combination with strained polyacrylamide gel alignment, Dipolar Waves can be used

18 Design of a poly-l-lysine conjugated polyacrylamide gel allows optimization of SDS-protein im

19 on the diffusion coefficients through 0.8 mm polyacrylamide gels, although they did increase with tem

20 tial gel permeation chromatography/acid-urea polyacrylamide gel analyses.

21 weight cutoff (MWCO) filter fabricated using polyacrylamide gel and (ii) covalent antibody immobiliza

22 mental observations obtained with the use of polyacrylamide gel and a microsphere indentation method

23 d by photo-patterning of two polymeric gels, polyacrylamide gel and polyethylene glycol (PEG) gel, on

24 ns, the electrophoretic mobility observed in polyacrylamide gels and in free solution decreases progr

25 When separated in polyacrylamide gels and stained with silver nanoparticle

26 rotein were collected from cells cultured on polyacrylamide gels and TCP and were analyzed for the ex

27 stimated from stained sodium dodecyl sulfate-polyacrylamide gels and verified by Western blotting and

28 g from 59 patients with adverse reactions to polyacrylamide gel, and 54 biopsies and 2 cytology speci

29 Polyacrylamide gels are cast upon a stiff support with c

30 A photopatterned free-standing polyacrylamide gel array comprised of 8 mm-scale polyacr

31 ng the riboswitch EMSAs on the free-standing polyacrylamide gel array, three design considerations we

32 iation across the large-format free-standing polyacrylamide gel array.

33 To optimize the discontinuous polyacrylamide gel assay format, we demonstrate developm

34 boflavin photochemical reduction system in a polyacrylamide gel assay, which was blocked by the Cu-Zn

35 Polyacrylamide gel copolymerized with a cationic polymer

36 Enzymographic assays used polyacrylamide gels copolymerized with denatured type I

37 onectin oligomers under native conditions in polyacrylamide gel coupled with methods for producing st

38 We have used protein electrophoresis through polyacrylamide gels derivatized with the proprietary lig

39 torage protein fractions, in one-dimensional polyacrylamide gel electrophoresis (1D-PAGE) and two-dim

40 us labrax) fillets using the two-dimensional polyacrylamide gel electrophoresis (2-DE) technique.

41 e max) root hair cells using two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) and shotgun

42 In this study, we used two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) and tandem

43 Two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) is the comm

44 roteomic analyses, including two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) separation

45 lectrophoresis (1D-PAGE) and two-dimensional polyacrylamide gel electrophoresis (2D-PAGE).

46 I-LHCII supercomplex isolated by blue native polyacrylamide gel electrophoresis (BN-PAGE) from digito

47 sis of PP2A and PP4 complexes by blue native polyacrylamide gel electrophoresis (BN-PAGE) indicates t

48 Blue native polyacrylamide gel electrophoresis (BN-PAGE) is a powerf

49 ize exclusion chromatography and blue native polyacrylamide gel electrophoresis (BN-PAGE) to demonstr

50 tion and one- or two-dimensional blue native polyacrylamide gel electrophoresis (BN-PAGE).

51 r mitochondria were subjected to blue native polyacrylamide gel electrophoresis (BNGE) to separate OX

52 achieved within 6h using continuous elution polyacrylamide gel electrophoresis (CE-PAGE) on commerci

53 sized using cetyl trimethylammonium bromide polyacrylamide gel electrophoresis (CTAB-PAGE), for subs

54 troduce a microfluidic free-standing kinetic polyacrylamide gel electrophoresis (fsKPAGE) assay.

55 isoelectric focusing sodium dodecyl sulfate polyacrylamide gel electrophoresis (IEF/SDS-PAGE) and fl

56 Therefore, we introduce a kinetic polyacrylamide gel electrophoresis (KPAGE) microfluidic

57 were synthesized and shown by nondenaturing polyacrylamide gel electrophoresis (native PAGE) to have

58 ding to FGF.FGFR complexes were subjected to polyacrylamide gel electrophoresis (PAGE) analysis and d

59 y has been proven to be successful by native polyacrylamide gel electrophoresis (PAGE) and cryogenic

60 rus core protein (HBcAg) was separated using polyacrylamide gel electrophoresis (PAGE) and electro-bl

61 s and the methods of mass spectrometry (MS), polyacrylamide gel electrophoresis (PAGE) and nuclear ma

62 Both native polyacrylamide gel electrophoresis (PAGE) and pore-limit

63 The method uses polyacrylamide gel electrophoresis (PAGE) followed by qu

64 Native polyacrylamide gel electrophoresis (PAGE) gel shifts as

65 using (TGF) and sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE) in a PDMS/glas

66 and label-free sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE) method for mea

67 Urea-polyacrylamide gel electrophoresis (PAGE) of partially d

68 cally optimize chemical lysis and subsequent polyacrylamide gel electrophoresis (PAGE) of the single-

69 separation matrix pore-size at the head of a polyacrylamide gel electrophoresis (PAGE) separation cha

70 Using polyacrylamide gel electrophoresis (PAGE) to separate mo

71 Native polyacrylamide gel electrophoresis (PAGE) was integrated

72 al microfluidic architecture that integrates polyacrylamide gel electrophoresis (PAGE) with immunoblo

73 of microfluidic networks and the utility of polyacrylamide gel electrophoresis (PAGE), we develop a

74 glutathiolate in water and then separated by polyacrylamide gel electrophoresis (PAGE).

75 aphy-tandem mass spectrometry (LC-MS/MS) and polyacrylamide gel electrophoresis (PAGE).

76 trometry (ICP MS), 1D sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS PAGE)-LA ICP MS,

77 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analyses o

78 Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophoresis (SDS-PAGE) analysis r

79 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis s

80 and characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and electr

81 ation (IP) pattern on sodium docecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and simila

82 samples by utilising sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) combined w

83 two portions: one for sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) fiber typi

84 omprises non-reducing sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) followed b

85 es into a nonreducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gel contai

86 The use of sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) helped the

87 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) is a widel

88 - and beta-tubulin by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) on minigel

89 h parallel capillary sodium dodecyl sulfate- polyacrylamide gel electrophoresis (SDS-PAGE) or capilla

90 A modified Laemmli sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) protocol i

91 Analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) revealed t

92 trategy that involves sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) separation

93 microscopy (AFM) and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) to investi

94 In addition, when sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was used d

95 Denaturing polyacrylamide gel electrophoresis (SDS-PAGE) was used t

96 epletion method (with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)) achieved

97 sized proteins after sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and enabl

98 ich were confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), oxidative

99 c mobility (shift) in sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), which was

100 graphy (SE-HPLC) and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE).

101 -IEF were analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE).

102 bilized trypsin using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE).

103 ere characterised by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE).

104 ion were verified via sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)/Western an

105 essed, they are separated via sodium dodecyl-polyacrylamide gel electrophoresis (SDS-PAGE, the second

106 n was carried out by sodium dodecyl sulphate polyacrylamide gel electrophoresis after pre-fractionati

107 mensional blue native-sodium dodecyl sulfate-polyacrylamide gel electrophoresis analyses showed that

108 using one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis and identifi

109 Two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis previously i

110 Blue native-polyacrylamide gel electrophoresis analysis showed that

111 hylakoids post cross linking and blue-native polyacrylamide gel electrophoresis analysis shows that T

112 orption mass spectrometry and by blue native polyacrylamide gel electrophoresis analysis.

113 Small angle X-ray scattering, native polyacrylamide gel electrophoresis and activity assays w

114 Native polyacrylamide gel electrophoresis and analytical gel fi

115 sly unidentified A-minor junctions by native polyacrylamide gel electrophoresis and atomic force micr

116 Co-affinity purification, non-denaturing polyacrylamide gel electrophoresis and bis(maleimido)hex

117 atic protein-SDS complexes formed during SDS polyacrylamide gel electrophoresis and brings a new tool

118 Results from blue native polyacrylamide gel electrophoresis and chemical cross-li

119 Two-dimensional blue native polyacrylamide gel electrophoresis and coimmunoprecipita

120 which is evaluated by sodium dodecyl sulfate polyacrylamide gel electrophoresis and corresponding Wes

121 imer was observed under native conditions by polyacrylamide gel electrophoresis and fast protein liqu

122 or the presence of inositol phosphates using polyacrylamide gel electrophoresis and high-performance

123 rized these protein complexes by blue native polyacrylamide gel electrophoresis and identified approx

124 eins were isolated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and identified by mas

125 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and image densitometr

126 n fragments were quantified with agarose and polyacrylamide gel electrophoresis and immunoblotting.

127 and analyzed by both sodium dodecyl sulfate polyacrylamide gel electrophoresis and immunofluorescenc

128 -L1; L4-S1) were retrieved and 2-dimensional polyacrylamide gel electrophoresis and immunohistocytoch

129 women (18-39 years old) by combining native-polyacrylamide gel electrophoresis and liquid chromatogr

130 ied as calmodulins by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and liquid chromatogr

131 Native polyacrylamide gel electrophoresis and mass spectrometry

132 gle band at 42 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and molecular ion at

133 ns by two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis and peptide mass fing

134 s are used in several applications including polyacrylamide gel electrophoresis and sensing devices.

135 d chimeric ORF50 proteins, using Blue Native polyacrylamide gel electrophoresis and size exclusion ch

136 ot analysis, immunohistochemistry, acid urea-polyacrylamide gel electrophoresis and sodium dodecyl su

137 by performing tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis and subsequent image

138 bility as a trimer on sodium dodecyl sulfate-polyacrylamide gel electrophoresis and the capacity to p

139 ents were first separated by two-dimensional polyacrylamide gel electrophoresis and then identified b

140 otein migration using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blotting

141 nventional methods of sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blotting

142 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and western-blot anal

143 The results of a native polyacrylamide gel electrophoresis assay using JR-FL tri

144 d disrupted NPM oligomer formation by native polyacrylamide gel electrophoresis assay.

145 gh its application in sodium dodecyl sulfate-polyacrylamide gel electrophoresis assays as well as sol

146 y gel mobility shift, beta-galactosidase and polyacrylamide gel electrophoresis assays identified a n

147 of Ebola virus NP by sodium dodecyl sulfate-polyacrylamide gel electrophoresis by 5 and 15 kDa, resp

148 man plaque tissues by sodium dodecyl sulfate polyacrylamide gel electrophoresis confirmed that the pr

149 tracentrifugation and sodium dodecyl sulfate polyacrylamide gel electrophoresis demonstrated that in

150 Polyacrylamide gel electrophoresis demonstrated that the

151 e protein mixtures by sodium dodecyl sulfate-polyacrylamide gel electrophoresis followed by in-gel di

152 Quantitative RT-PCR and 2-dimensional polyacrylamide gel electrophoresis followed by MALDI/TOF

153 One-dimensional polyacrylamide gel electrophoresis followed by nanocapil

154 Using high-resolution polyacrylamide gel electrophoresis for analysis of wall

155 s were separated on a sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel after tandem affi

156 tein extracted from a sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel and subjected to

157 chagasic sera and on sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels stained with sil

158 of gH, gB, and gD in sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels was altered by d

159 of thylakoid preparations directly in native polyacrylamide gel electrophoresis gels, enabling unprec

160 RNA polyacrylamide gel electrophoresis identified 94 (50%) s

161 Blue native polyacrylamide gel electrophoresis identified PCFT dimer

162 , followed by two-dimensional sodium dodecyl polyacrylamide gel electrophoresis identified several ca

163 tection of simian picobirnaviruses (PBVs) by polyacrylamide gel electrophoresis in fecal specimens of

164 gonal two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis method to probe biolo

165 s of tau with altered sodium dodecyl sulfate-polyacrylamide gel electrophoresis migration have a grea

166 ining components with sodium dodecyl sulfate-polyacrylamide gel electrophoresis mobilities that resem

167 ins exhibited similar sodium dodecyl sulfate-polyacrylamide gel electrophoresis mobilities, indicatin

168 ionation coupled with sodium dodecyl sulfate polyacrylamide gel electrophoresis mobility assays enabl

169 s with reactive counterparts and analyzed by polyacrylamide gel electrophoresis mobility shifts.

170 possessed an M(r) on sodium dodecyl sulfate-polyacrylamide gel electrophoresis of 38,500.

171 cells using specific enzymatic assays, urea-polyacrylamide gel electrophoresis of cell extracts, and

172 Two-dimensional polyacrylamide gel electrophoresis of CSF from normal su

173 Blue native-polyacrylamide gel electrophoresis of mitochondrial extr

174 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of proteins associate

175 a single-cell targeted proteomic assay with polyacrylamide gel electrophoresis of single cell lysate

176 Moreover, polyacrylamide gel electrophoresis of the enriched extra

177 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles of transglut

178 ize-exclusion chromatography and blue native polyacrylamide gel electrophoresis revealed a modular Ba

179 tract was realized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis SDS-PAGE-immunoblotti

180 Sodium dodecyl sulfate polyacrylamide gel electrophoresis showed modification w

181 Blue native polyacrylamide gel electrophoresis studies revealed that

182 Agarose and polyacrylamide gel electrophoresis systems for the molec

183 m spectroscopy, Dynamic Light Scattering and Polyacrylamide Gel Electrophoresis techniques were used

184 esis method as an alternative to traditional polyacrylamide gel electrophoresis to characterize nucle

185 We used polyacrylamide gel electrophoresis to compare the extent

186 '-radiolabeled DNA substrates and denaturing polyacrylamide gel electrophoresis to provide evidence f

187 Nondenaturing polyacrylamide gel electrophoresis verified that apoA-V(

188 Blue native polyacrylamide gel electrophoresis was used to isolate a

189 By using improved polyacrylamide gel electrophoresis we were able to visua

190 l electrophoresis and sodium dodecyl sulfate-polyacrylamide gel electrophoresis Western blotting, rev

191 and analysis by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis with different concen

192 gel-based separation (sodium dodecyl sulfate-polyacrylamide gel electrophoresis) and analysis by liqu

193 shed FDF-PAGE (fully-denaturing formaldehyde polyacrylamide gel electrophoresis) to prevent annealing

194 rotein backbones (via sodium dodecyl sulfate-polyacrylamide gel electrophoresis).

195 chromatography) and 2D-PAGE (two-dimensional polyacrylamide gel electrophoresis).

196 The samples are resolved by native polyacrylamide gel electrophoresis, after which fluoresc

197 bikunin GAG mixture obtained by preparative polyacrylamide gel electrophoresis, allowed the determin

198 d by circular dichroism spectroscopy, native polyacrylamide gel electrophoresis, and enzyme-linked im

199 acterized concerning size by gel filtration, polyacrylamide gel electrophoresis, and mass spectrometr

200 ate targets were resolved by two-dimensional polyacrylamide gel electrophoresis, and phosphorylated g

201 c and quasi-elastic light scattering, native polyacrylamide gel electrophoresis, and ultracentrifugat

202 ichroism spectroscopy, native and denaturing polyacrylamide gel electrophoresis, and UV-visible-near-

203 hosphoprotein staining after two-dimensional polyacrylamide gel electrophoresis, as well as column-ba

204 at protein as seen by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, as well as the great

205 rchitecture at the molecular level by native polyacrylamide gel electrophoresis, as well as the netwo

206 KCNQ4 subunits, as reported by nondenaturing polyacrylamide gel electrophoresis, at C643 at the end o

207 structures have been characterized by native polyacrylamide gel electrophoresis, atomic force microsc

208 racterized by multiple techniques, including polyacrylamide gel electrophoresis, dynamic light scatte

209 ion and separation by sodium dodecyl sulfate polyacrylamide gel electrophoresis, followed by autoradi

210 Immunoprecipitation and blue native polyacrylamide gel electrophoresis, followed by immunobl

211 s were resolved using sodium dodecyl sulfate-polyacrylamide gel electrophoresis, followed by staining

212 Blue native polyacrylamide gel electrophoresis, gel filtration, and

213 on microscopy, dynamic light scattering, and polyacrylamide gel electrophoresis, is reported for the

214 ologic binding assay, sodium dodecyl sulfate polyacrylamide gel electrophoresis, mass spectrometry, a

215 nonreduced capillary sodium dodecyl sulfate polyacrylamide gel electrophoresis, reversed-phase high-

216 By using blue native/Deriphat-polyacrylamide gel electrophoresis, sucrose density grad

217 Amino acid chromatographic analysis, polyacrylamide gel electrophoresis, UV-Vis spectrophotom

218 g, size exclusion chromatography, and native polyacrylamide gel electrophoresis, we demonstrate that

219 Using two dimensional polyacrylamide gel electrophoresis, we demonstrated that

220 Last, using polyacrylamide gel electrophoresis, we showed that added

221 A 2-dimensional polyacrylamide gel electrophoresis-based comparative pro

222 In this study, we have developed a polyacrylamide gel electrophoresis-based screening metho

223 HRG was confirmed by sodium dodecyl sulphate polyacrylamide gel electrophoresis-Western blot and size

224 tion of proteins, followed by sodium dodecyl-polyacrylamide gel electrophoresis.

225 HP genotype was determined by polyacrylamide gel electrophoresis.

226 mately 25 kDa on 12% sodium dodecyl sulphate-polyacrylamide gel electrophoresis.

227 d using different extracts and conducted SDS-polyacrylamide gel electrophoresis.

228 rhoea attributable to rotavirus with EIAs or polyacrylamide gel electrophoresis.

229 as a stain for visualizing nucleic acids in polyacrylamide gel electrophoresis.

230 by gel permeation chromatography and native-polyacrylamide gel electrophoresis.

231 on and quantitation of proteins separated by polyacrylamide gel electrophoresis.

232 s were resolved using sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

233 rate as the wild-type AcrB trimer in native polyacrylamide gel electrophoresis.

234 or the 58-kDa size by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

235 ed by one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

236 based on non-reducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

237 immunohistochemical analysis and blue native polyacrylamide gel electrophoresis.

238 id chromatography and sodium dodecyl sulfate polyacrylamide gel electrophoresis.

239 motile cells, as assessed by two-dimensional polyacrylamide gel electrophoresis.

240 was determined using sodium dodecyl sulfate-polyacrylamide gel electrophoresis/N-terminal sequencing

241 vine serum; SDS-PAGE, sodium dodecyl sulfate-polyacrylamide gel electrophoresis; RANKL, receptor acti

242 95% pure as judged by sodium dodecyl sulfate-polyacrylamide gel electrophoretic analysis and was free

243 rRNA gene sequencing, sodium dodecyl sulfate-polyacrylamide gel electrophoretic analysis of whole-cel

244 olution regional photopatterning of multiple polyacrylamide gel elements, and automated electrophoret

245 The free-standing polyacrylamide gel EMSAs yielded reliable quantification

246 slide supporting a 30-mum-thick photoactive polyacrylamide gel enables western blotting: settling of

247 ins and integrins on fibronectin (FN)-coated polyacrylamide gels (FN-PAG) and on FN-coated pillars us

248 method that uses highly porous, nongradient polyacrylamide gels for separation of rat brain mitochon

249 Reaction products are electrophoresed on polyacrylamide gels for visualization and quantitation b

250 microfluidic card comprised of free-standing polyacrylamide gel (fsPAG) separation lanes supports 384

251 alyte" capture strategy introduced here uses polyacrylamide gel grafted with concentrated point charg

252 In the present work, polyacrylamide gel has been used as a matrix for the imm

253 ry amines, (ii) electrophoretic migration in polyacrylamide gels, (iii) quantification of methylene d

254 otocol describes regional photopatterning of polyacrylamide gels in glass microfluidic devices as a p

255 pitulated by varying the matrix stiffness of polyacrylamide gels in the range of normal and fibrotic

256 ensional blue native/lithium dodecyl sulfate-polyacrylamide gels indicated that no intact PS II monom

257 l complexation obtained by SDS-PAGE on a 10% polyacrylamide gel, it was observed that the polyphenols

258 es along the length of a single freestanding polyacrylamide gel lane of varying cross-sectional width

259 n and stress field within the bulk of a thin polyacrylamide gel layer indented by a millimeter-size g

260 e involves the preparation of functionalized polyacrylamide gels loaded with fluorescent beads, as we

261 conducted to detect CK17 trapped in a porous polyacrylamide gel matrix have highlighted the specific

262 etween a 3D fibrillar ECM and an ECM-coupled polyacrylamide gel of defined compliance, allowing the s

263 Using this method, we analyzed polyacrylamide gels of different stiffness and assessed

264 oach was verified by measuring the moduli of polyacrylamide gels of known stiffness.

265 Using polyacrylamide gels of physiologically relevant elastici

266 responses of HaCaT keratinocytes seeded upon polyacrylamide gels of three stiffnesses (1, 30, and 100

267 chanical properties using fibronectin-coated polyacrylamide gels of varying physiologic stiffness, pl

268 thelial cells were cultured at confluence on polyacrylamide gels of varying stiffness and treated wit

269 matrix assembled by cells grown on FN-coated polyacrylamide gels of varying stiffnesses showed that r

270 3T3 fibroblasts on fibronectin (FN)-modified polyacrylamide gels of varying thickness reveals signifi

271 used this platform to track NIH 3T3 cells on polyacrylamide gels over 20 hrs.

272 The resulting chip consists of 40 polyacrylamide gel pad array units for the immobilizatio

273 n, we utilize a photopatterned free-solution-polyacrylamide gel (PAG) stacking interface at the head

274 ay of microwells molded in a thin layer of a polyacrylamide gel (PAG).

275 In a native polyacrylamide gel, Pgp3 purified from a bacterial expre

276 emonstrates mechanosensing by T cells, using polyacrylamide gels presenting ligands to CD3 and CD28.

277 TiO2 samples were synthesized via a modified polyacrylamide gel route using different aluminum salts,

278 Using native polyacrylamide gel shift assay and negative-stain EM, we

279 acrylamide gel array comprised of 8 mm-scale polyacrylamide gel strips acts as a chassis for 96 concu

280 ting evaporation from the open free-standing polyacrylamide gel structures during electrophoresis, an

281 Experiments with synthetic polyacrylamide gel substrates implicate both specific ex

282 yosin inhibition on lung tissue with that of polyacrylamide gels suggests that matrix fiber organizat

283 igonucleotide copolymerized into a 6% linear polyacrylamide gel that captures ssDNA or dsDNA analyte

284 icrofluidic channel housing a photopatterned polyacrylamide gel that incorporates a photoactive benzo

285 tic immunoassays, we introduce discontinuous polyacrylamide gels that enable quantitative assay compl

286 n deposited onto fibronectin-coated glass or polyacrylamide gels, they adhere and spread by protrudin

287 of isoelectric focusing in a large pore-size polyacrylamide gel to determine protein pI followed by i

288 biophysical properties of the functionalized polyacrylamide gels upon which these cells are cultured.

289 channel-filling benzophenone-functionalized polyacrylamide gel via brief UV exposure (photoblot), fo

290 formance of BECC and Sneddon's model on thin polyacrylamide gels, we find that although Sneddon's mod

291 trate porosity without altering stiffness in polyacrylamide gels, we show that varying substrate poro

292 sses as low as approximately 5 kDa, gradient polyacrylamide gels were superior.

293 ism, electron microscopy, and native and SDS-polyacrylamide gels were used to demonstrate alpha-synuc

294 , direct immobilization of active trypsin in polyacrylamide gel will compromise the protein separatio

295 vercome this problem, here we report a novel polyacrylamide gel with switchable trypsin activity.

296 cular myocytes for 7 days on collagen-coated polyacrylamide gels with varying elastic moduli.

297 y canine kidney epithelial cells cultured on polyacrylamide gels with varying rigidity and treated wi

298 easurements carried out using fibroblasts on polyacrylamide gels with Young's moduli ranging from 6 t

299 l pre-stress with culture on stiff (7.5 kPa) polyacrylamide gels (with or without transforming growth

300 o collagen and fibrin gels than they do into polyacrylamide gels, with the latter exhibiting characte