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1 s neoglycolipids and their robust display on nitrocellulose.
2 to cytochrome b(558) that has been bound to nitrocellulose.
3 bumin electroblotted from SDS-PAGE gels onto nitrocellulose.
4 nst antigens blotted from SDS-PAGE gels onto nitrocellulose.
5 crylamide gel electrophoresis and blotted to nitrocellulose.
6 on of the dehydrated/rehydrated liposomes on nitrocellulose.
7 in chimeras also bound to MG2 immobilized on nitrocellulose.
8 ned hepatocyte membrane proteins absorbed on nitrocellulose.
9 fied RHL-1 but not to RHL-2/3 immobilized on nitrocellulose.
10 s to dissociate electroblotted proteins from nitrocellulose.
11 ing histidine-tagged proteins immobilized on nitrocellulose.
12 ll lysate following SDS-PAGE and transfer to nitrocellulose.
13 herichia coli, were arrayed and spotted onto nitrocellulose.
14 protein bovine serum albumin immobilized on nitrocellulose.
15 n a MALDI plate that had been precoated with nitrocellulose.
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
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
25 s were separated by SDS-PAGE, transferred to nitrocellulose and probed with alkaline phosphatase-labe
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
35 concentration and extraction technique, onto nitrocellulose-based paper microfluidic devices with the
37 lver stained, or the proteins transferred to nitrocellulose blots and probed with either tryptase-spe
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 additive for one-step enzymatic digestion of nitrocellulose-bound proteins, both in terms of highest
43 purified chick brain myosin-V absorbed onto nitrocellulose-coated cover slips inhibited the ability
47 of protein chips using derivatized glass and nitrocellulose-coated slides and the employment of recom
49 finity of DNA substrates was measured by the nitrocellulose-DEAE double filter binding assay, binding
50 conclusion, this study demonstrates that the nitrocellulose-DEX coating can effectively attenuate the
53 e peptides are added directly to a sample of nitrocellulose dissolved in acetone, allowing them to in
55 NA were studied by stopped-flow kinetics and nitrocellulose equilibrium DNA binding experiments in th
56 phite electrodes modified with an insulating nitrocellulose film and is evoked after the cellulase tr
59 n anticancer drugs and the type II enzyme, a nitrocellulose filter assay was used to characterize the
64 COX-2 ARE binding activity was determined by nitrocellulose filter binding and UV cross-linking assay
70 complementary fluorescence spectroscopic and nitrocellulose filter binding assays to quantitate the r
78 te size is about 50 nt, a value confirmed by nitrocellulose filter binding under stoichiometric condi
79 gel electrophoresis-band mobility shift, and nitrocellulose filter binding, were established to study
81 -resistant mutant topoisomerase IV proteins, nitrocellulose filter DNA binding assays, and KMnO4 prob
84 5 antibody to conjunctival cells obtained by nitrocellulose filter paper stripping (impression cytolo
85 SRP components by using gel retardation and nitrocellulose filter-binding assays and enzymatic analy
89 racterization of Nova-2 in RNA selection and nitrocellulose filter-binding assays reveals that Nova-2
90 is study, we used RNA gel mobility shift and nitrocellulose filter-binding assays to further investig
92 sed by using 4,146 cellular cDNAs arrayed on nitrocellulose filters and real-time reverse transcripti
94 troplax membrane, and (ii) subsequent use of nitrocellulose filters to which both the membrane-bound
95 by a modified plaque lift approach in which nitrocellulose filters were coated with an anti-immunogl
96 ut they do proceed further in development on nitrocellulose filters, forming defective fruiting bodie
97 mutants display almost normal development on nitrocellulose filters, producing multi-tipped aggregate
103 ples were electrophoresed and transferred to nitrocellulose for detection by avidin conjugated to alk
105 ffer solution continuously through paper and nitrocellulose, from a buffer reservoir at one end of th
107 belled FlgN from Salmonella typhimurium with nitrocellulose-immobilized cell lysates of wild-type S.
108 ng Mel-CAM-negative SBcl-2 cells, adhered to nitrocellulose-immobilized Mel-CAM produced by baculovir
109 a soluble recombinant form (sCAR), bound to nitrocellulose-immobilized virions from the different su
110 on-membrane digestion by dissolution of the nitrocellulose in MALDI matrix solution containing 70% a
111 these organic compounds on nitrocellulose as nitrocellulose is also soluble in most of the organic so
116 -conglutin immobilized on the test line of a nitrocellulose membrane and beta-conglutin in the test s
117 nsideration the optical characteristics of a nitrocellulose membrane and gold nanoparticles on an LFA
118 he protein is easily reversible in 2 min for nitrocellulose membrane and in 10 min for PVDF membrane
119 rticular, the protein sample is spotted onto nitrocellulose membrane and then subjected to a solid-ph
126 lobulin G (GAM) antibody were sprayed onto a nitrocellulose membrane in strips at positions designate
127 etary technology is a capture layer, where a nitrocellulose membrane is modified with the target anal
128 he penetration behavior of the liquid in the nitrocellulose membrane may (partly) explain the distrib
129 LFIA) was based on the immobilization onto a nitrocellulose membrane of an ovalbumin-CPPU conjugate (
132 blotting, samples were directly blotted onto nitrocellulose membrane soaked in Nd(2)(SO(4))(3) buffer
133 state levels of MCP-1 mRNA within 3 h after nitrocellulose membrane stab or implant injury to the ad
134 ay, CT was detected as a colored band on the nitrocellulose membrane strip, where CT bound to GM1-lip
137 s were dispensed onto separate test zones of nitrocellulose membrane to serve as capture reagents.
138 s, transferred onto a Nd(2)(SO(4))(3)-soaked nitrocellulose membrane using a phosphate buffer system,
140 biomolecules within the spot embedded in the nitrocellulose membrane was analyzed by confocal laser s
142 ng with amido black of protein dots bound to nitrocellulose membrane with lowest protein measurements
144 tive gel, separated, capillary eluted onto a nitrocellulose membrane, and recovered using the matrix
145 found that the minimized Mie scattering from nitrocellulose membrane, consequently maximizes the Rayl
146 lamide gel electrophoresis, transferred to a nitrocellulose membrane, dissolved in acetone/trifluoroa
147 one protein was denatured and immobilized on nitrocellulose membrane, indicating a direct and stable
151 S gel electrophoresis, and renaturation on a nitrocellulose membrane, strongly suggesting that phosph
153 ed dots at the test and control zones of the nitrocellulose membrane, while negative samples resulted
162 ngth GSDMB and the N-terminal domain bind to nitrocellulose membranes immobilized with phosphoinositi
163 is not observed in protein overlay assays on nitrocellulose membranes in which a Grb2 fusion protein
165 e obtained from normal volunteers using pure nitrocellulose membranes rather than cellulose acetate.
166 e we describe an immunoblotting method using nitrocellulose membranes that allows quantitative analys
167 videnced by the facts that this DNA bound to nitrocellulose membranes under nondenaturing conditions,
169 directly spotted onto pre-Ponceau S-stained nitrocellulose membranes, cross-linked with glutaraldehy
171 matrix components from a tissue surface onto nitrocellulose membranes, generating a two-dimensional a
172 d from mucosal epithelium and immobilized on nitrocellulose membranes, N. meningitidis attached predo
173 d S8, did not bind any components present on nitrocellulose membranes, presumably because S7 and S8 a
179 MCF7 human breast cancers were spotted onto nitrocellulose microarrays and hybridized with mouse and
182 e immobilized onto chitosan (CHIT) activated nitrocellulose (NC) membrane via glutaraldehyde coupling
183 h an antigen detection scheme that employs a nitrocellulose (NC) membrane with 200 nm pore size to ca
187 cence-based method for detecting proteins on nitrocellulose or polyvinylidene difluoride (PVDF) membr
188 mponents were identified after flocculation (nitrocellulose) or precipitation (sawdust, CaCO3, and fl
191 to characterise the fluid flow of different nitrocellulose paper strips after oxygen-plasma treatmen
193 fofuse") is a strip of the flammable polymer nitrocellulose patterned with alkali metal ions; this pa
194 ase assay, on a set of model surfaces, i.e., nitrocellulose, polystyrene, poly(methyl methacrylate),
195 rotease per 1 microliter buffer per 1 mm2 of nitrocellulose; relatively large pieces of membrane (> o
198 idylglycerol, or cardiolipin) are blotted on nitrocellulose sheets (Eastern blot) prior to transfer o
200 us and doughnut-like on the FAST and Unisart nitrocellulose slides, whereas a better spot morphology
204 mes and the test sample and a plastic-backed nitrocellulose strip with a measurement zone were used i
206 oparticle distribution across the supporting nitrocellulose strip, therefore enabling on-stick contro
207 d 80% of the liposomes were recovered on the nitrocellulose strips after a cycle of dehydration and r
210 ted with immobilized ribosomal P antigens on nitrocellulose strips; affinity-purified fractions were
212 the human immunodeficiency virus 1 system on nitrocellulose substrates illustrate the usefulness and
214 irst separated by SDS-PAGE, transferred to a nitrocellulose support membrane, and probed with a panel
217 s in proximity to HRP protein immobilized on nitrocellulose to improve the sensitivity for this model
218 ay (DRaCALA), is based on the ability of dry nitrocellulose to separate the free ligand from bound pr
220 h native RACK-1 that had been immobilized on nitrocellulose, UV-treated control PKC alpha bound well
221 ]GTP to four small G proteins immobilized on nitrocellulose was competed by a series of analogues wit
222 to several purified annexins immobilized on nitrocellulose was determined by detection with horserad
223 s (e.g., conjugation, sample, absorption and nitrocellulose), were placed in a different configuratio
224 odine receptor binds to triadin blotted onto nitrocellulose with a KD of 40 nM in a medium containing
225 del system, flames propagate along strips of nitrocellulose with one of two possible modes of propaga
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