ライフサイエンスコーパス: nitrocellulose

1 n a MALDI plate that had been precoated with nitrocellulose.

2 s neoglycolipids and their robust display on nitrocellulose.

3 to cytochrome b(558) that has been bound to nitrocellulose.

4 bumin electroblotted from SDS-PAGE gels onto nitrocellulose.

5 nst antigens blotted from SDS-PAGE gels onto nitrocellulose.

6 crylamide gel electrophoresis and blotted to nitrocellulose.

7 on of the dehydrated/rehydrated liposomes on nitrocellulose.

8 protein bovine serum albumin immobilized on nitrocellulose.

9 in chimeras also bound to MG2 immobilized on nitrocellulose.

10 ned hepatocyte membrane proteins absorbed on nitrocellulose.

11 fied RHL-1 but not to RHL-2/3 immobilized on nitrocellulose.

12 s to dissociate electroblotted proteins from nitrocellulose.

13 ing histidine-tagged proteins immobilized on nitrocellulose.

14 ll lysate following SDS-PAGE and transfer to nitrocellulose.

15 herichia coli, were arrayed and spotted onto nitrocellulose.

16 The proteins, electroblotted onto nitrocellulose after SDS--PAGE separation and stained wi

17 binds species specifically to EJ dotted onto nitrocellulose, an mAb to REJ induces the sperm AR, anti

18 in I interaction using apoA-I immobilized on nitrocellulose and annexin I in solution with binding de

19 separation, the proteins were transferred to nitrocellulose and detected with either pooled sera gene

20 Porous media made of nitrocellulose and glass fiber are common "paper" substr

21 oader dynamic range compared with commercial nitrocellulose and glass substrates.

22 polyadenylated RNA, followed by transfer to nitrocellulose and hybridization to cloned onc probes sh

23 stain by which proteins can be visualized on nitrocellulose and polyvinylidine fluoride (PVDF) membra

24 The biotin tag is detected on both nitrocellulose and positively charged nylon membranes by

25 s were separated by SDS-PAGE, transferred to nitrocellulose and probed with alkaline phosphatase-labe

26 First, it was determined that nitrocellulose and PVDF membranes gave significantly low

27 edure is applicable only to protein blots on nitrocellulose and PVDF membranes.

28 l Ponceau S staining of the protein spots on nitrocellulose and quantification of the protein-dye com

29 The protein fragments were transferred to nitrocellulose, and biotinylated nitrilotriacetic acid w

30 naturing gel electrophoresis, transferred to nitrocellulose, and probed for avidin-reactive species.

31 are resolved by SDS--PAGE and transferred to nitrocellulose, and the region of the blot corresponding

32 immobilization of these organic compounds on nitrocellulose as nitrocellulose is also soluble in most

33 o polysaccharides and oligosaccharides using nitrocellulose-based CBM macroarrays and microtiter plat

34 In this study, we developed a nitrocellulose-based coating for the local delivery of t

35 concentration and extraction technique, onto nitrocellulose-based paper microfluidic devices with the

36 ctor (eIF) 4F and eIF(iso)4F, as measured by nitrocellulose binding and fluorescence titration.

37 lver stained, or the proteins transferred to nitrocellulose blots and probed with either tryptase-spe

38 MBP-obscurin bound recombinant GST-sAnk1 in nitrocellulose blots.

39 coli antigens were tested for reactivity to nitrocellulose-blotted extract from purified HDM bodies,

40 to 17 months regarding IgE autoreactivity to nitrocellulose-blotted human epithelial cell extracts an

41 We transfer scWestern separations to a nitrocellulose blotting medium with distinct mass transf

42 additive for one-step enzymatic digestion of nitrocellulose-bound proteins, both in terms of highest

43 le-sided adhesive support; and (iv) a porous nitrocellulose/cellulose acetate membrane.

44 purified chick brain myosin-V absorbed onto nitrocellulose-coated cover slips inhibited the ability

45 Chimeric selectins were adsorbed to nitrocellulose-coated glass beads on a coverslip.

46 First, printing of five CPSs onto nitrocellulose-coated glass slides was tested.

47 ribed and translated in vitro and printed on nitrocellulose-coated glass slides.

48 cking the C-terminal lipid-binding domain on nitrocellulose-coated glass surfaces and full-length con

49 10F12.3) to tether skeletal muscle myosin to nitrocellulose-coated glass.

50 ted and each diluted version is spotted on a nitrocellulose-coated slide in triplicate.

51 of protein chips using derivatized glass and nitrocellulose-coated slides and the employment of recom

52 1,824 fractions were spotted in duplicate on nitrocellulose-coated slides.

53 finity of DNA substrates was measured by the nitrocellulose-DEAE double filter binding assay, binding

54 conclusion, this study demonstrates that the nitrocellulose-DEX coating can effectively attenuate the

55 Silicon neural probes with and without nitrocellulose-DEX coatings were implanted into rat brai

56 ccessible to the ferricyanide reaction after nitrocellulose digestion by cellulase.

57 e peptides are added directly to a sample of nitrocellulose dissolved in acetone, allowing them to in

58 -affinity-purified antibodies, and ELF using nitrocellulose-eluted antibodies.

59 NA were studied by stopped-flow kinetics and nitrocellulose equilibrium DNA binding experiments in th

60 phite electrodes modified with an insulating nitrocellulose film and is evoked after the cellulase tr

61 the surface of a MALDI probe tip via a thin nitrocellulose film.

62 labeled immuno-aptamer sandwich applied onto nitrocellulose-film-modified electrodes digested the fil

63 a soluble redox indicator, ferricyanide, on nitrocellulose films treated by cellulases.

64 n anticancer drugs and the type II enzyme, a nitrocellulose filter assay was used to characterize the

65 150 mM potassium glutamate, pH 8.0, using a nitrocellulose filter assay.

66 Using both nitrocellulose filter binding and fluorescence assays, w

67 Nitrocellulose filter binding and gel mobility shift ass

68 Nitrocellulose filter binding and kinetic burst assays s

69 COX-2 ARE binding activity was determined by nitrocellulose filter binding and UV cross-linking assay

70 Nitrocellulose filter binding assay and equilibrium fluo

71 Using the nitrocellulose filter binding assay, the koff of recombi

72 f its "natural" substrate, glycine tRNA in a nitrocellulose filter binding assay.

73 ecrease in ATP binding was confirmed using a nitrocellulose filter binding assay.

74 Nitrocellulose filter binding assays (NCFBAs) have been

75 complementary fluorescence spectroscopic and nitrocellulose filter binding assays to quantitate the r

76 RNase footprinting and nitrocellulose filter binding assays were previously use

77 Using RNase footprinting and nitrocellulose filter binding assays, we detected a high

78 Using nitrocellulose filter binding assays, we determined that

79 Gel mobility shift and nitrocellulose filter binding experiments indicate that

80 Rapid mixing and nitrocellulose filter binding reveal that the binding co

81 Nitrocellulose filter binding studies show that UvrD bin

82 protein-bound DNA populations using standard nitrocellulose filter binding techniques.

83 te size is about 50 nt, a value confirmed by nitrocellulose filter binding under stoichiometric condi

84 gel electrophoresis-band mobility shift, and nitrocellulose filter binding, were established to study

85 termined using fluorescence spectroscopy and nitrocellulose filter binding.

86 -resistant mutant topoisomerase IV proteins, nitrocellulose filter DNA binding assays, and KMnO4 prob

87 a biotinylated bovine serum albumin-blocked nitrocellulose filter membrane with streptavidin.

88 ein microarrays printed on protein-permeable nitrocellulose filter membranes.

89 5 antibody to conjunctival cells obtained by nitrocellulose filter paper stripping (impression cytolo

90 SRP components by using gel retardation and nitrocellulose filter-binding assays and enzymatic analy

91 We used nitrocellulose filter-binding assays and real-time biose

92 Results of nitrocellulose filter-binding assays demonstrate that th

93 Both gel shift and nitrocellulose filter-binding assays provided evidence t

94 racterization of Nova-2 in RNA selection and nitrocellulose filter-binding assays reveals that Nova-2

95 is study, we used RNA gel mobility shift and nitrocellulose filter-binding assays to further investig

96 Here we use fluorescence, nitrocellulose filter-binding, and DNase I-sensitivity a

97 sed by using 4,146 cellular cDNAs arrayed on nitrocellulose filters and real-time reverse transcripti

98 T-NO2Ura-tRNA complexes could be isolated on nitrocellulose filters or by SDS-PAGE.

99 troplax membrane, and (ii) subsequent use of nitrocellulose filters to which both the membrane-bound

100 by a modified plaque lift approach in which nitrocellulose filters were coated with an anti-immunogl

101 ut they do proceed further in development on nitrocellulose filters, forming defective fruiting bodie

102 mutants display almost normal development on nitrocellulose filters, producing multi-tipped aggregate

103 cterial lawns and arrests as loose mounds on nitrocellulose filters.

104 errant in plaques on bacterial lawns than on nitrocellulose filters.

105 in yeast colonies replicated to and lysed on nitrocellulose filters.

106 yvalent than monovalent phosphoinositides on nitrocellulose filters.

107 , and hence a local electric field, within a nitrocellulose flow channel.

108 ples were electrophoresed and transferred to nitrocellulose for detection by avidin conjugated to alk

109 lyvinylidene difluoride membrane rather than nitrocellulose for immunoblotting.

110 ffer solution continuously through paper and nitrocellulose, from a buffer reservoir at one end of th

111 on with protein standards placed on the same nitrocellulose grid.

112 belled FlgN from Salmonella typhimurium with nitrocellulose-immobilized cell lysates of wild-type S.

113 ng Mel-CAM-negative SBcl-2 cells, adhered to nitrocellulose-immobilized Mel-CAM produced by baculovir

114 These results suggest the compatibility of nitrocellulose-immobilized scWesterns with a variety of

115 a soluble recombinant form (sCAR), bound to nitrocellulose-immobilized virions from the different su

116 on-membrane digestion by dissolution of the nitrocellulose in MALDI matrix solution containing 70% a

117 these organic compounds on nitrocellulose as nitrocellulose is also soluble in most of the organic so

118 Our findings show that ITP on nitrocellulose is capable of up to a 900 fold increase i

119 The nitrocellulose is incubated in colloidal gold suspension

120 The nitrocellulose is patterned with wax to form 25 isolated

121 The nitrocellulose lies horizontally on a working electrode,

122 ntibody against the pathogen was coated on a nitrocellulose membrane (NCM) where the test line was co

123 -conglutin immobilized on the test line of a nitrocellulose membrane and beta-conglutin in the test s

124 nsideration the optical characteristics of a nitrocellulose membrane and gold nanoparticles on an LFA

125 The capture antibody (cAb) printing onto nitrocellulose membrane and gold-labelled detection anti

126 he protein is easily reversible in 2 min for nitrocellulose membrane and in 10 min for PVDF membrane

127 rticular, the protein sample is spotted onto nitrocellulose membrane and then subjected to a solid-ph

128 isolated by spotting the crude reaction on a nitrocellulose membrane and then washing.

129 ynthesis of ADSP and the fabrication of ADSP nitrocellulose membrane array can be completed on the sa

130 This approach is demonstrated in nitrocellulose membrane as well as paper, and the added

131 and sensitive detection of 100 nm FNDs on a nitrocellulose membrane at a particle density of 0.04 ng

132 In the IB method, a nitrocellulose membrane blot of surface growth was react

133 We show that ITP on the nitrocellulose membrane can be powered and run several t

134 h immuno-complex which is later spotted on a nitrocellulose membrane coated slide.

135 supramolecular probe (ADSP) is coated onto a nitrocellulose membrane for array-based capture and to e

136 nd rabbit anti-sheep IgG were immobilized on nitrocellulose membrane for the test line and control li

137 Nitrocellulose membrane functionalized with globular hyd

138 This pH meter consists of I) a nitrocellulose membrane impregnated with a pH-sensitive

139 lobulin G (GAM) antibody were sprayed onto a nitrocellulose membrane in strips at positions designate

140 vation of both parasite and human DNA on the nitrocellulose membrane inside the RDT was stable even a

141 components with the gold conjugates and the nitrocellulose membrane is minimized.

142 etary technology is a capture layer, where a nitrocellulose membrane is modified with the target anal

143 he penetration behavior of the liquid in the nitrocellulose membrane may (partly) explain the distrib

144 LFIA) was based on the immobilization onto a nitrocellulose membrane of an ovalbumin-CPPU conjugate (

145 ion of inkjet printed biomolecules in porous nitrocellulose membrane pads of different brands.

146 nd distribution of the immune complex in the nitrocellulose membrane slides.

147 blotting, samples were directly blotted onto nitrocellulose membrane soaked in Nd(2)(SO(4))(3) buffer

148 state levels of MCP-1 mRNA within 3 h after nitrocellulose membrane stab or implant injury to the ad

149 ay, CT was detected as a colored band on the nitrocellulose membrane strip, where CT bound to GM1-lip

150 mplex is then allowed to migrate upward on a nitrocellulose membrane strip.

151 We studied electrophoresis on 50 x 4 mm nitrocellulose membrane strips utilized in LFIA.

152 ,5-bisphosphate-containing lipid vesicles or nitrocellulose membrane strips.

153 functionalized pPy particles coalesce on the nitrocellulose membrane to produce a chemiresistive band

154 s were dispensed onto separate test zones of nitrocellulose membrane to serve as capture reagents.

155 s, transferred onto a Nd(2)(SO(4))(3)-soaked nitrocellulose membrane using a phosphate buffer system,

156 This system was easily fabricated on a nitrocellulose membrane using a wax-printing method and

157 biomolecules within the spot embedded in the nitrocellulose membrane was analyzed by confocal laser s

158 Nitrocellulose membrane was chosen as the substrate to s

159 First, the dot-blot immunoassay on a nitrocellulose membrane was optimized for the quantitati

160 ng with amido black of protein dots bound to nitrocellulose membrane with lowest protein measurements

161 The strip detection step uses a nitrocellulose membrane with streptavidin and immunoglob

162 tive gel, separated, capillary eluted onto a nitrocellulose membrane, and recovered using the matrix

163 imetric, lateral flow assays consisting of a nitrocellulose membrane, are the preferred format today

164 found that the minimized Mie scattering from nitrocellulose membrane, consequently maximizes the Rayl

165 lamide gel electrophoresis, transferred to a nitrocellulose membrane, dissolved in acetone/trifluoroa

166 one protein was denatured and immobilized on nitrocellulose membrane, indicating a direct and stable

167 Nitrocellulose membrane, precoated with anti-LH, was soa

168 After transfer of the proteins to a nitrocellulose membrane, probing with coat protein-speci

169 yphi O901 and an anti-IgG were dotted on the nitrocellulose membrane, respectively.

170 S gel electrophoresis, and renaturation on a nitrocellulose membrane, strongly suggesting that phosph

171 A strip of a nitrocellulose membrane, that contains the substrate, is

172 ed dots at the test and control zones of the nitrocellulose membrane, while negative samples resulted

173 re resolved by SDS-PAGE and immobilized on a nitrocellulose membrane.

174 esult from CNBr digestion of proteins on the nitrocellulose membrane.

175 adhesion of the target protein to the solid nitrocellulose membrane.

176 7 kDa carrier protein to immobilize onto the nitrocellulose membrane.

177 ibody solution followed by a CRP solution in nitrocellulose membrane.

178 micropipets; this device did not damage the nitrocellulose membrane.

179 yphi O901 and antibody of S. typhi O901 on a nitrocellulose membrane.

180 Initially, seeds were germinated on nitrocellulose membranes and antibody secretion detected

181 Calibrants were made of nitrocellulose membranes doped with lanthanide standards

182 mide gel electrophoresis, and transferred to nitrocellulose membranes for immunoblot analysis.

183 ngth GSDMB and the N-terminal domain bind to nitrocellulose membranes immobilized with phosphoinositi

184 is not observed in protein overlay assays on nitrocellulose membranes in which a Grb2 fusion protein

185 products to the capture spacers attached to nitrocellulose membranes or to microspheres.

186 e obtained from normal volunteers using pure nitrocellulose membranes rather than cellulose acetate.

187 e we describe an immunoblotting method using nitrocellulose membranes that allows quantitative analys

188 videnced by the facts that this DNA bound to nitrocellulose membranes under nondenaturing conditions,

189 ined users; ii) A new approach for producing nitrocellulose membranes with integrated electrodes that

190 agnostic test developers using cellulose and nitrocellulose membranes with limited fluid sample volum

191 on 7.5% polyacrylamide gels, transferred to nitrocellulose membranes, and probed for Fos.

192 directly spotted onto pre-Ponceau S-stained nitrocellulose membranes, cross-linked with glutaraldehy

193 Several nitrocellulose membranes, each functionalized with a dif

194 matrix components from a tissue surface onto nitrocellulose membranes, generating a two-dimensional a

195 d from mucosal epithelium and immobilized on nitrocellulose membranes, N. meningitidis attached predo

196 d S8, did not bind any components present on nitrocellulose membranes, presumably because S7 and S8 a

197 h the adsorption of plasmid DNA to nylon and nitrocellulose membranes.

198 electrophoresis and transfer of proteins to nitrocellulose membranes.

199 ands by exponential enrichment (SELEX) using nitrocellulose membranes.

200 ectable by conventional immunoblotting using nitrocellulose membranes.

201 ucleotides such as ATP, bind irreversibly to nitrocellulose membranes.

202 MCF7 human breast cancers were spotted onto nitrocellulose microarrays and hybridized with mouse and

203 expressed proteins are printed directly onto nitrocellulose microarrays without purification.

204 Nitroglycerin (NG) and nitrocellulose (NC) are constituents of double-base prop

205 Nitrocellulose (NC) is widely used in both military and

206 ica-core gold nanoshells (GNSs) preloaded in nitrocellulose (NC) membrane as model lateral flow immun

207 e immobilized onto chitosan (CHIT) activated nitrocellulose (NC) membrane via glutaraldehyde coupling

208 h an antigen detection scheme that employs a nitrocellulose (NC) membrane with 200 nm pore size to ca

209 roteins that have been electroblotted onto a nitrocellulose (NC) membrane.

210 ifferent types of paper substrates including nitrocellulose, nylon, poly(vinylidene fluoride), and ce

211 specimens were processed by applying liquid nitrocellulose on exposed surfaces.

212 g to PDE5 was retained when filtered through nitrocellulose or glass-fiber membranes.

213 cence-based method for detecting proteins on nitrocellulose or polyvinylidene difluoride (PVDF) membr

214 mponents were identified after flocculation (nitrocellulose) or precipitation (sawdust, CaCO3, and fl

215 each sample are arrayed onto glass-supported nitrocellulose pads.

216 me (2 mul) of protein solution is applied to nitrocellulose paper in a grid array and dried.

217 to characterise the fluid flow of different nitrocellulose paper strips after oxygen-plasma treatmen

218 CNF penetrate inside the pores of LFs nitrocellulose paper, compacting the pore size only in t

219 ing of colloidal gold to proteins adhered to nitrocellulose paper.

220 fofuse") is a strip of the flammable polymer nitrocellulose patterned with alkali metal ions; this pa

221 ase assay, on a set of model surfaces, i.e., nitrocellulose, polystyrene, poly(methyl methacrylate),

222 rotease per 1 microliter buffer per 1 mm2 of nitrocellulose; relatively large pieces of membrane (> o

223 The method involves the production of nitrocellulose replica filter lifts from a plasmid cDNA

224 Nitrocellulose sequesters proteins and bound ligand at t

225 idylglycerol, or cardiolipin) are blotted on nitrocellulose sheets (Eastern blot) prior to transfer o

226 ver 1,000 samples may be printed on a single nitrocellulose slide.

227 us and doughnut-like on the FAST and Unisart nitrocellulose slides, whereas a better spot morphology

228 icroarray immunoassay was performed on these nitrocellulose slides.

229 behavior of a liquid droplet on and in these nitrocellulose slides.

230 A simple plastic-backed nitrocellulose strip is the basis for an assay for detec

231 mes and the test sample and a plastic-backed nitrocellulose strip with a measurement zone were used i

232 On the nitrocellulose strip, antisense-reporter probes are immo

233 oparticle distribution across the supporting nitrocellulose strip, therefore enabling on-stick contro

234 d 80% of the liposomes were recovered on the nitrocellulose strips after a cycle of dehydration and r

235 th specific nucleotide probes immobilized on nitrocellulose strips.

236 antibodies immobilized in a defined zone on nitrocellulose strips.

237 ted with immobilized ribosomal P antigens on nitrocellulose strips; affinity-purified fractions were

238 ods to develop a microarray of DNA probes on nitrocellulose substrate are discussed.

239 nversion nanoparticle (UCNP) labels from the nitrocellulose substrate.

240 the human immunodeficiency virus 1 system on nitrocellulose substrates illustrate the usefulness and

241 Compared to state-of-the-art glass and nitrocellulose substrates, assays on synthetic paper pro

242 id flow dynamics of a droplet on the various nitrocellulose substrates.

243 irst separated by SDS-PAGE, transferred to a nitrocellulose support membrane, and probed with a panel

244 We designed a nitrocellulose-surface microarray containing human cytok

245 After LDS-PAGE and transfer to nitrocellulose these proteins bind [32P]GTP in the prese

246 s in proximity to HRP protein immobilized on nitrocellulose to improve the sensitivity for this model

247 ay (DRaCALA), is based on the ability of dry nitrocellulose to separate the free ligand from bound pr

248 l overlay of untreated and sialidase-treated nitrocellulose transfers, respectively.

249 oreover, we pattern hydrophobic regions onto nitrocellulose using the wax printing method and form on

250 h native RACK-1 that had been immobilized on nitrocellulose, UV-treated control PKC alpha bound well

251 ]GTP to four small G proteins immobilized on nitrocellulose was competed by a series of analogues wit

252 to several purified annexins immobilized on nitrocellulose was determined by detection with horserad

253 s (e.g., conjugation, sample, absorption and nitrocellulose), were placed in a different configuratio

254 odine receptor binds to triadin blotted onto nitrocellulose with a KD of 40 nM in a medium containing

255 del system, flames propagate along strips of nitrocellulose with one of two possible modes of propaga

256 Results showed that nitrocellulose yielded the greatest assay sensitivity re