ライフサイエンスコーパス: polyacrylamide

1 resence of O2 inhibits the polymerization of polyacrylamide.

2 tion, as indicated by the electrophoresis in polyacrylamide/agarose gel profile.

3 source of background, we embedded samples in polyacrylamide, anchored RNAs to this polyacrylamide mat

4 A hydrogel-dielectric-elastomer system, polyacrylamide and poly(dimethylsiloxane) (PDMS), is ada

5 ar weight additives (ethylene glycol, linear polyacrylamide and poly(ethylene oxide)) were investigat

6 was also extended to the study of blends of polyacrylamide and poly(N,N-dimethylacrylamide) homopoly

7 We use polyacrylamide and poly(N-isopropylacrylamide) precursor

8 M) commonly takes place on materials such as polyacrylamide- and polyethylene glycol-based gels.

9 (CIAP) immobilized in benzophenone-modified polyacrylamide (BPMA-PAAm) gel films housed in an array

10 se, MnP and LiP entrapped, respectively into polyacrylamide/carboxymethylcellulose (CMC).

11 A newly developed polyacrylamide-co-methyl acrylate/spiropyran (SP) hydrog

12 ctor was synthesized and coupled to a linear polyacrylamide coated capillary for online sample prepar

13 d polymer network than the conventional 7.5% polyacrylamide concentration and supports the fabricatio

14 An 18% polyacrylamide concentration is shown to provide for a m

15 hrough in situ polymerization of polystyrene-polyacrylamide copolymers is established.

16 As such, this study reports the use of polyacrylamide cryogel, loaded with Cu(2+) (through the

17 (ECs) on collagen-coupled stiff or compliant polyacrylamide ECMs to examine the effects of MCAK expre

18 ectivity (boric acid) and efficiency (linear polyacrylamide) enhancing additives.

19 i))(n) (e.g., gel electrophoresis, CGE using polyacrylamide-filled capillaries) are its resolution, c

20 ucing long-term infection in the presence of polyacrylamide filler in cosmetic surgery, possibly due

21 r was prepared by Cat-Ru immobilization in a polyacrylamide film.

22 zyme-laden agarose gels which are stamped on polyacrylamide films containing immobilized substrates a

23 While no aqueous removal of polyacrylamide friction reducer was observed over a peri

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

63 Using polyacrylamide gel electrophoresis (PAGE) to separate mo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 Blue native-polyacrylamide gel electrophoresis analysis showed that

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

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

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

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

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

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

101 Two-dimensional blue native polyacrylamide gel electrophoresis and coimmunoprecipita

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

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

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

105 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and image densitometr

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

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

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

109 Native polyacrylamide gel electrophoresis and mass spectrometry

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

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

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

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

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

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

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

117 Polyacrylamide gel electrophoresis demonstrated that the

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

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

120 Blue native polyacrylamide gel electrophoresis identified PCFT dimer

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

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

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

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

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

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

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

128 Blue native-polyacrylamide gel electrophoresis of mitochondrial extr

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

130 Moreover, polyacrylamide gel electrophoresis of the enriched extra

131 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles of transglut

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

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

134 Sodium dodecyl sulfate polyacrylamide gel electrophoresis showed modification w

135 Blue native polyacrylamide gel electrophoresis studies revealed that

136 Agarose and polyacrylamide gel electrophoresis systems for the molec

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

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

139 We used polyacrylamide gel electrophoresis to compare the extent

140 Nondenaturing polyacrylamide gel electrophoresis verified that apoA-V(

141 Blue native polyacrylamide gel electrophoresis was used to isolate a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

156 Blue native polyacrylamide gel electrophoresis, gel filtration, and

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

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

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

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

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

162 Using two dimensional polyacrylamide gel electrophoresis, we demonstrated that

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

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

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

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

167 immunohistochemical analysis and blue native polyacrylamide gel electrophoresis.

168 id chromatography and sodium dodecyl sulfate polyacrylamide gel electrophoresis.

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

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

171 HP genotype was determined by polyacrylamide gel electrophoresis.

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

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

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

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

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

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

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

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

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

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

182 The free-standing polyacrylamide gel EMSAs yielded reliable quantification

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

203 tep after dehydrating the antigen-containing polyacrylamide gel.

204 ng a photoactive benzophenone methacrylamide polyacrylamide gel.

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

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

207 microwells located in a approximately 40 mum polyacrylamide gel.

208 , MnP and LiP encapsulated respectively into polyacrylamide/ gelatine and to 87%, 91%, 87% for laccas

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

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

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

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

213 Polyacrylamide gels are cast upon a stiff support with c

214 Enzymographic assays used polyacrylamide gels copolymerized with denatured type I

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

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

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

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

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

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

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

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

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

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

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

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

227 3T3 fibroblasts on fibronectin (FN)-modified polyacrylamide gels of varying thickness reveals signifi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

243 or application in both aqueous solutions and polyacrylamide gels.

244 xes that were readily detected on denaturing polyacrylamide gels.

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

246 ng properties compared to existing ultrathin polyacrylamide gels.

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

248 fixing methylene blue bands in nucleic acid polyacrylamide gels.

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

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

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

252 -Eps15) fusion proteins immobilized within a polyacrylamide hydrogel as a substrate for quantifying E

253 hat uses gradients of ions between miniature polyacrylamide hydrogel compartments bounded by a repeat

254 stion, we have developed and characterized a polyacrylamide hydrogel culture platform featuring highl

255 Here, we present the use of polyacrylamide hydrogel films containing built-in chemic

256 ratiometric 30 nm oxygen nanosensors made of polyacrylamide hydrogel, near-infrared (NIR) luminescent

257 HTM cells were cultured on polyacrylamide hydrogels possessing values for complianc

258 ese cellular responses on fibronectin-coated polyacrylamide hydrogels prepared at a physiologic range

259 low-cost, robust method was used to produce polyacrylamide hydrogels with stiffness gradients of 0.5

260 ost widely used soft cell culture substrate, polyacrylamide hydrogels, and show that stem cells respo

261 collagen and fibrin that is not observed in polyacrylamide, in facilitating mechanosensing over long

262 gnitude lower than that of commercial linear polyacrylamide (LPA)-coated capillaries.

263 The degradation of aminomethylated polyacrylamide (Mannich) polymer used for sludge treatme

264 les in polyacrylamide, anchored RNAs to this polyacrylamide matrix, and cleared cellular proteins and

265 Narrow pH-specific polyacrylamide membranes are photopatterned in situ for

266 reparation functionality via small pore size polyacrylamide membranes is also key to automated operat

267 An immuno-reactive filter, macroporous polyacrylamide monolith (PAM), fabricated within a micro

268 glet oxygen probe was covalently linked to a polyacrylamide nanoparticle core using different archite

269 5-(and-6)-Carboxylic Acid, encapsulated into polyacrylamide nanoparticles with surface modification f

270 ors are encapsulated inside porous and inert polyacrylamide nanoparticles.

271 However, cells on polyacrylamide of low elastic modulus (0.5 kPa) could no

272 ured on flat and wedge-shaped gels made from polyacrylamide or cross-linked collagen.

273 st validated by means of elastomeric models (polyacrylamide or polydimethylsiloxane) of a soft inclus

274 of linear sieving additives, such as linear polyacrylamide or polyethylene oxide, hinders the introd

275 Polyacrylamide (PA) based hydrogels are used in several

276 roduce microfluidic 2DE using photopatterned polyacrylamide (PA) gel elements housed in a millimeter-

277 esis from those microwells into a supporting polyacrylamide (PA) gel layer, and in-gel antibody probi

278 Using mechanically tunable polyacrylamide (PA) gels functionalized with the extrace

279 in a single, straight microchannel housing a polyacrylamide (PA) pore-size gradient gel.

280 tem cells on polydimethylsiloxane (PDMS) and polyacrylamide (PAAm) hydrogel surfaces, 0.1 kPa-2.3 MPa

281 Polyacrylamide (PAM) based friction reducers are a prima

282 e diffusion coefficients (D) of plutonium in polyacrylamide (PAM) gel and found D in the range of 2.0

283 effective diffusion coefficients of Pu(V) in polyacrylamide (PAM) gel in the presence of humic acid u

284 Polydimethylsiloxane (PDMS) and Polyacrylamide (PAm) hydrogel have been chosen as soft p

285 on-the-fly KMC model for the degradation of polyacrylamide (PAM) using UV light and titanium dioxide

286 was applied for the preparation of swellable polyacrylamide particles incorporating silver nanopartic

287 93% for laccase, MnP and LiP entrapped into Polyacrylamide/pectin, 94%, 98%, 88% for laccase, MnP an

288 dy to follistatin was first immobilized in a polyacrylamide PLE gradient gel, near the origin of the

289 sticide detection employing a functionalized polyacrylamide, polyhydroxamicalkanoate (PHA), which mim

290 how that copolymerization of collagen I with polyacrylamide produces minimal matrix models of scars (

291 rior to injection of nondegradable gels like polyacrylamide should be explored as well.

292 icropatterned single hiPSC-CMs on deformable polyacrylamide substrates containing fluorescent microbe

293 tran penetration measurements indicated that polyacrylamide substrates of low elastic modulus were mo

294 Single hPSC-CMs were cultured on polyacrylamide substrates of physiological stiffness (10

295 ler cell line was cultured on laminin-coated polyacrylamide substrates with calibrated Young's moduli

296 s solution and subsequently immobilized in a polyacrylamide thin film to construct a random single-mo

297 , and 22 kDa at sample loads of 0.5 mug (for polyacrylamide) to 2.5 mug (for agarose).

298 rporation of plasma membrane proteins into a polyacrylamide "tube gel" followed by in-gel digestion o

299 ate appropriately on both agarose and native polyacrylamide, unlike many currently available DNA ladd

300 Parameters such as the percent polyacrylamide used in hydrogel construction as well as