ライフサイエンスコーパス: polyacrylamide

1 resence of O2 inhibits the polymerization of polyacrylamide.

2 etic cellulose (33.3%), polypropylene (25%), polyacrylamides (10%) and polyester (8.3%).

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

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

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

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

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

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

9 d high-throughput synthesis and screening of polyacrylamide-based excipients to yield a formulation w

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

11 gamma-FeOOH graphene polyacrylamide carbonized aerogel (gamma-FeOOH GPCA) wit

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

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

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

15 Polyacrylamide-coated, carbon nanotube (PA/CNT) electrod

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

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

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

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

20 f both polyethylene glycol-DNA (PEG-DNA) and polyacrylamide-DNA (PA-DNA) hydrogels, as well as their

21 g as degradable electrical fuses, and (iv) a polyacrylamide-DNA hydrogel operating as a fluidic valve

22 sing DNA-anchored compounds, (ii) degradable polyacrylamide-DNA hydrogels encapsulating nanoparticles

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

24 e characterized using sodium dodecyl sulfate polyacrylamide electrophoresis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

41 Polyacrylamide gel copolymerized with a cationic polymer

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

59 Polyacrylamide Gel Electrophoresis (PAGE) and Latex Aggl

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

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

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

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

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

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

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

67 Using polyacrylamide gel electrophoresis (PAGE) to separate mo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

96 Two-dimensional blue native polyacrylamide gel electrophoresis and coimmunoprecipita

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

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

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

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

101 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and image densitometr

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

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

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

105 Native polyacrylamide gel electrophoresis and mass spectrometry

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

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

108 Native polyacrylamide gel electrophoresis and size exclusion ch

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

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

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

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

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

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

115 Sodium dodecyl sulfate polyacrylamide gel electrophoresis demonstrated that 60%

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

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

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

119 Blue native polyacrylamide gel electrophoresis identified PCFT dimer

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

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

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

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

124 Blue native-polyacrylamide gel electrophoresis of mitochondrial extr

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

126 Moreover, polyacrylamide gel electrophoresis of the enriched extra

127 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles of transglut

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

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

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

131 Sodium dodecyl sulfate polyacrylamide gel electrophoresis showed modification w

132 Blue native polyacrylamide gel electrophoresis studies revealed that

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

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

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

136 Blue native polyacrylamide gel electrophoresis was used to isolate a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

159 Using two dimensional polyacrylamide gel electrophoresis, we demonstrated that

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

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

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

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

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

165 immunohistochemical analysis and blue native polyacrylamide gel electrophoresis.

166 id chromatography and sodium dodecyl sulfate polyacrylamide gel electrophoresis.

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

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

169 HP genotype was determined by polyacrylamide gel electrophoresis.

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

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

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

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

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

175 The free-standing polyacrylamide gel EMSAs yielded reliable quantification

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

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

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

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

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

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

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

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

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

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

186 Native polyacrylamide gel shift analysis did suggest that Bap1

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

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

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

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

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

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

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

194 Hydrophilic polyacrylamide gel was injected into the soft palate of

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

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

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

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

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

200 tep after dehydrating the antigen-containing polyacrylamide gel.

201 ng a photoactive benzophenone methacrylamide polyacrylamide gel.

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

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

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

205 microwells located in a approximately 40 mum polyacrylamide gel.

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

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

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

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

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

211 Polyacrylamide gels are cast upon a stiff support with c

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

237 or application in both aqueous solutions and polyacrylamide gels.

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

239 xes that were readily detected on denaturing polyacrylamide gels.

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

241 ng properties compared to existing ultrathin polyacrylamide gels.

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

243 fixing methylene blue bands in nucleic acid polyacrylamide gels.

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

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

246 artition coefficients across a wide range of polyacrylamide hydrogel densities (R(2) = 0.98).

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

248 e cooling of a lithium- and bromine-enriched polyacrylamide hydrogel.

249 For example, two pieces of alginate-polyacrylamide hydrogels achieve adhesion energies about

250 Linearly elastic polyacrylamide hydrogels and polydimethylsiloxane (PDMS)

251 Using tunable polyacrylamide hydrogels of extreme stiffnesses, we meas

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

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

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

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

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

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

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

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

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

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

262 Lightly crosslinked fluorescently doped polyacrylamide nanogels were subsequently produced by hi

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

264 rs can further be enhanced by using cationic polyacrylamide nanoparticles as a delivery vehicle.

265 5-(and-6)-Carboxylic Acid, encapsulated into polyacrylamide nanoparticles with surface modification f

266 ors are encapsulated inside porous and inert polyacrylamide nanoparticles.

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

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

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

270 Polyacrylamide (PA) based hydrogels are used in several

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

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

273 We modulated polyacrylamide (PA) gel pore size via lateral chain aggr

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

275 In this work, we used polyacrylamide (PA) gels with varying stiffness (6.5-92.

276 rehydration of lipid films deposited on soft polyacrylamide (PAA) gels.

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

278 ctional behavior for polyacrylic acid (PAA), polyacrylamide (PAAm), and agarose hydrogel spheres on s

279 Polyacrylamide (PAM) based friction reducers are a prima

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

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

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

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

284 uminum-based coagulants compared to cationic polyacrylamide (PAM).

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

286 93% for laccase, MnP and LiP entrapped into Polyacrylamide/pectin, 94%, 98%, 88% for laccase, MnP an

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

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

289 yrene particle solution (colloidal fouling), polyacrylamide polymer solution (organic fouling) and a

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