ライフサイエンスコーパス: polyacrylamide gel

1 ng a photoactive benzophenone methacrylamide polyacrylamide gel.

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

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

4 nalized microwells formed in a thin layer of polyacrylamide gel.

5 microwells located in a approximately 40 mum polyacrylamide gel.

6 tep after dehydrating the antigen-containing polyacrylamide gel.

7 or application in both aqueous solutions and polyacrylamide gels.

8 xes that were readily detected on denaturing polyacrylamide gels.

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

10 ng properties compared to existing ultrathin polyacrylamide gels.

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

12 fixing methylene blue bands in nucleic acid polyacrylamide gels.

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

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

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

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

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

18 ve hydrogels, but exceed those in unmodified polyacrylamide gels.

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

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

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

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

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

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

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

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

27 When separated in polyacrylamide gels and stained with silver nanoparticle

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

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

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

31 (VEGF-165), integrate with glass coverslips, polyacrylamide gels, and collagen scaffolds, enable acti

32 Polyacrylamide gels are cast upon a stiff support with c

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

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

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

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

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

38 Polyacrylamide gel copolymerized with a cationic polymer

39 Enzymographic assays used polyacrylamide gels copolymerized with denatured type I

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

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

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

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

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

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

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

47 ish species was separated by two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), and the to

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

49 d is introduced that is based on Blue Native Polyacrylamide Gel Electrophoresis (BN-PAGE) and dot imm

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

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

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

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

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

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

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

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

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

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

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

61 g metal ion contaminant sweeping-blue native-polyacrylamide gel electrophoresis (MICS-BN-PAGE).

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

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

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

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

66 thoroughly characterized such DNA motifs by polyacrylamide gel electrophoresis (PAGE) and fluorescen

67 Polyacrylamide Gel Electrophoresis (PAGE) and Latex Aggl

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

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

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

71 Native polyacrylamide gel electrophoresis (PAGE) gel shifts as

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

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

74 olding and PTMs is difficult because routine polyacrylamide gel electrophoresis (PAGE) methods lack t

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

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

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

78 Using polyacrylamide gel electrophoresis (PAGE) to separate mo

79 Native polyacrylamide gel electrophoresis (PAGE) was integrated

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

81 rovide high mobilities of glycoconjugates on polyacrylamide gel electrophoresis (PAGE), as compared w

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

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

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

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

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

87 The sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis o

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

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

90 ity was determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and matrix

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

116 Blue native-polyacrylamide gel electrophoresis analysis showed that

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

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

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

120 Native polyacrylamide gel electrophoresis and analytical gel fi

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

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

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

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

125 Two-dimensional blue native polyacrylamide gel electrophoresis and coimmunoprecipita

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

127 lysis, using combined sodium dodecyl sulfate-polyacrylamide gel electrophoresis and high-performance

128 ceable separation on sodium dodecyl sulphate-polyacrylamide gel electrophoresis and high-performance

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

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

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

132 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and image densitometr

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

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

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

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

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

138 osin alpha-4 chain (TPM4) by two-dimensional polyacrylamide gel electrophoresis and mass spectrometry

139 Native polyacrylamide gel electrophoresis and mass spectrometry

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

141 Native polyacrylamide gel electrophoresis and size exclusion ch

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

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

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

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

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

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

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

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

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

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

152 torage were identified using two-dimensional polyacrylamide gel electrophoresis coupled with matrix-a

153 Sodium dodecyl sulfate polyacrylamide gel electrophoresis demonstrated that 60%

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

155 Polyacrylamide gel electrophoresis demonstrated that the

156 One-dimensional polyacrylamide gel electrophoresis followed by nanocapil

157 ng (to quantify total (32)P-activity) and by polyacrylamide gel electrophoresis followed by phosphori

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

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

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

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

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

171 Blue native-polyacrylamide gel electrophoresis of mitochondrial extr

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

173 Moreover, polyacrylamide gel electrophoresis of the enriched extra

174 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles of transglut

175 Based on native MS and polyacrylamide gel electrophoresis results, the abundanc

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

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

178 Sodium dodecyl sulfate polyacrylamide gel electrophoresis showed modification w

179 Blue native polyacrylamide gel electrophoresis studies revealed that

180 Agarose and polyacrylamide gel electrophoresis systems for the molec

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

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

183 We used polyacrylamide gel electrophoresis to compare the extent

184 on cell wall composition, we used GC-MS and polyacrylamide gel electrophoresis to measure cell-wall

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

186 Nondenaturing polyacrylamide gel electrophoresis verified that apoA-V(

187 Blue native polyacrylamide gel electrophoresis was used to isolate a

188 ing size exclusion chromatography and native polyacrylamide gel electrophoresis we demonstrated that

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 a, which migrates on sodium dodecyl sulphate polyacrylamide gel electrophoresis with a molecular weig

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

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

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

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

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

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

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

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

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

207 using a combined approach of non-denaturing polyacrylamide gel electrophoresis, dynamic light scatte

208 bination of in vitro techniques (TWJ-screen, polyacrylamide gel electrophoresis, fluorescence resonan

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 Blue native polyacrylamide gel electrophoresis, gel filtration, and

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

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

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

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

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

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

218 Using two dimensional polyacrylamide gel electrophoresis, we demonstrated that

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

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

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

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

223 immunohistochemical analysis and blue native polyacrylamide gel electrophoresis.

224 id chromatography and sodium dodecyl sulfate polyacrylamide gel electrophoresis.

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

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

227 HP genotype was determined by polyacrylamide gel electrophoresis.

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

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

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

231 be used as a general SDS replacement in SDS-polyacrylamide gel electrophoresis.

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

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

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

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

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

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

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

239 95% pure as judged by sodium dodecyl sulfate-polyacrylamide gel electrophoretic analysis and was free

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

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

242 The free-standing polyacrylamide gel EMSAs yielded reliable quantification

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

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

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

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

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

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

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

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

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

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

253 g hydrophilic cellulose membranes instead of polyacrylamide gel is used for the electrophoretic separ

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

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

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

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

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

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

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

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

262 Using polyacrylamide gels of physiologically relevant elastici

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

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

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

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

267 3T3 fibroblasts on fibronectin (FN)-modified polyacrylamide gels of varying thickness reveals signifi

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

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

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

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

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

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

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

275 Native polyacrylamide gel shift analysis did suggest that Bap1

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

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

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

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

280 ze solute interactions with a UV photoactive polyacrylamide gel that incorporates a benzophenone meth

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

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

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

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

285 Using fibronectin-coated polyacrylamide gels to alter substrate rigidity without

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

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

288 Hydrophilic polyacrylamide gel was injected into the soft palate of

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

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

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

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

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

294 The 3D microfluidic device is a photoactive polyacrylamide gel with a microwell array-patterned face

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