戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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.
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 additive for one-step enzymatic digestion of nitrocellulose-bound proteins, both in terms of highest
42 le-sided adhesive support; and (iv) a porous nitrocellulose/cellulose acetate membrane.
43  purified chick brain myosin-V absorbed onto nitrocellulose-coated cover slips inhibited the ability
44          Chimeric selectins were adsorbed to nitrocellulose-coated glass beads on a coverslip.
45 ribed and translated in vitro and printed on nitrocellulose-coated glass slides.
46 ted and each diluted version is spotted on a nitrocellulose-coated slide in triplicate.
47 of protein chips using derivatized glass and nitrocellulose-coated slides and the employment of recom
48 1,824 fractions were spotted in duplicate on nitrocellulose-coated slides.
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
51       Silicon neural probes with and without nitrocellulose-DEX coatings were implanted into rat brai
52 ccessible to the ferricyanide reaction after nitrocellulose digestion by cellulase.
53 e peptides are added directly to a sample of nitrocellulose dissolved in acetone, allowing them to in
54 -affinity-purified antibodies, and ELF using nitrocellulose-eluted antibodies.
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
57  the surface of a MALDI probe tip via a thin nitrocellulose film.
58  a soluble redox indicator, ferricyanide, on nitrocellulose films treated by cellulases.
59 n anticancer drugs and the type II enzyme, a nitrocellulose filter assay was used to characterize the
60  150 mM potassium glutamate, pH 8.0, using a nitrocellulose filter assay.
61                                   Using both nitrocellulose filter binding and fluorescence assays, w
62                                              Nitrocellulose filter binding and gel mobility shift ass
63                                              Nitrocellulose filter binding and kinetic burst assays s
64 COX-2 ARE binding activity was determined by nitrocellulose filter binding and UV cross-linking assay
65                                              Nitrocellulose filter binding assay and equilibrium fluo
66                                    Using the nitrocellulose filter binding assay, the koff of recombi
67 f its "natural" substrate, glycine tRNA in a nitrocellulose filter binding assay.
68 ecrease in ATP binding was confirmed using a nitrocellulose filter binding assay.
69                                              Nitrocellulose filter binding assays (NCFBAs) have been
70 complementary fluorescence spectroscopic and nitrocellulose filter binding assays to quantitate the r
71                       RNase footprinting and nitrocellulose filter binding assays were previously use
72                 Using RNase footprinting and nitrocellulose filter binding assays, we detected a high
73                                        Using nitrocellulose filter binding assays, we determined that
74                       Gel mobility shift and nitrocellulose filter binding experiments indicate that
75                             Rapid mixing and nitrocellulose filter binding reveal that the binding co
76                                              Nitrocellulose filter binding studies show that UvrD bin
77 protein-bound DNA populations using standard nitrocellulose filter binding techniques.
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
80 termined using fluorescence spectroscopy and nitrocellulose filter binding.
81 -resistant mutant topoisomerase IV proteins, nitrocellulose filter DNA binding assays, and KMnO4 prob
82  a biotinylated bovine serum albumin-blocked nitrocellulose filter membrane with streptavidin.
83 ein microarrays printed on protein-permeable nitrocellulose filter membranes.
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
86                                      We used nitrocellulose filter-binding assays and real-time biose
87                                   Results of nitrocellulose filter-binding assays demonstrate that th
88                           Both gel shift and nitrocellulose filter-binding assays provided evidence t
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
91                    Here we use fluorescence, nitrocellulose filter-binding, and DNase I-sensitivity a
92 sed by using 4,146 cellular cDNAs arrayed on nitrocellulose filters and real-time reverse transcripti
93 T-NO2Ura-tRNA complexes could be isolated on nitrocellulose filters or by SDS-PAGE.
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
98 cterial lawns and arrests as loose mounds on nitrocellulose filters.
99 errant in plaques on bacterial lawns than on nitrocellulose filters.
100 in yeast colonies replicated to and lysed on nitrocellulose filters.
101 yvalent than monovalent phosphoinositides on nitrocellulose filters.
102 , and hence a local electric field, within a nitrocellulose flow channel.
103 ples were electrophoresed and transferred to nitrocellulose for detection by avidin conjugated to alk
104 lyvinylidene difluoride membrane rather than nitrocellulose for immunoblotting.
105 ffer solution continuously through paper and nitrocellulose, from a buffer reservoir at one end of th
106 on with protein standards placed on the same nitrocellulose grid.
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
112                Our findings show that ITP on nitrocellulose is capable of up to a 900 fold increase i
113                                          The nitrocellulose is incubated in colloidal gold suspension
114                                          The nitrocellulose is patterned with wax to form 25 isolated
115                                          The nitrocellulose lies horizontally on a working electrode,
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
120 isolated by spotting the crude reaction on a nitrocellulose membrane and then washing.
121             This approach is demonstrated in nitrocellulose membrane as well as paper, and the added
122                          In the IB method, a nitrocellulose membrane blot of surface growth was react
123                      We show that ITP on the nitrocellulose membrane can be powered and run several t
124 h immuno-complex which is later spotted on a nitrocellulose membrane coated slide.
125                                              Nitrocellulose membrane functionalized with globular hyd
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 (
130 ion of inkjet printed biomolecules in porous nitrocellulose membrane pads of different brands.
131 nd distribution of the immune complex in the nitrocellulose membrane slides.
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
135 mplex is then allowed to migrate upward on a nitrocellulose membrane strip.
136 ,5-bisphosphate-containing lipid vesicles or nitrocellulose membrane strips.
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,
139       This system was easily fabricated on a nitrocellulose membrane using a wax-printing method and
140 biomolecules within the spot embedded in the nitrocellulose membrane was analyzed by confocal laser s
141                                              Nitrocellulose membrane was chosen as the substrate to s
142 ng with amido black of protein dots bound to nitrocellulose membrane with lowest protein measurements
143              The strip detection step uses a nitrocellulose membrane with streptavidin and immunoglob
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
148                                              Nitrocellulose membrane, precoated with anti-LH, was soa
149          After transfer of the proteins to a nitrocellulose membrane, probing with coat protein-speci
150 yphi O901 and an anti-IgG were dotted on the nitrocellulose membrane, respectively.
151 S gel electrophoresis, and renaturation on a nitrocellulose membrane, strongly suggesting that phosph
152                                 A strip of a nitrocellulose membrane, that contains the substrate, is
153 ed dots at the test and control zones of the nitrocellulose membrane, while negative samples resulted
154 re resolved by SDS-PAGE and immobilized on a nitrocellulose membrane.
155 esult from CNBr digestion of proteins on the nitrocellulose membrane.
156 ibody solution followed by a CRP solution in nitrocellulose membrane.
157  micropipets; this device did not damage the nitrocellulose membrane.
158 yphi O901 and antibody of S. typhi O901 on a nitrocellulose membrane.
159          Initially, seeds were germinated on nitrocellulose membranes and antibody secretion detected
160                      Calibrants were made of nitrocellulose membranes doped with lanthanide standards
161 mide gel electrophoresis, and transferred to nitrocellulose membranes for immunoblot analysis.
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
164  products to the capture spacers attached to nitrocellulose membranes or to microspheres.
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,
168  on 7.5% polyacrylamide gels, transferred to nitrocellulose membranes, and probed for Fos.
169  directly spotted onto pre-Ponceau S-stained nitrocellulose membranes, cross-linked with glutaraldehy
170                                      Several nitrocellulose membranes, each functionalized with a dif
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
174 h the adsorption of plasmid DNA to nylon and nitrocellulose membranes.
175  electrophoresis and transfer of proteins to nitrocellulose membranes.
176 ands by exponential enrichment (SELEX) using nitrocellulose membranes.
177 ectable by conventional immunoblotting using nitrocellulose membranes.
178 ucleotides such as ATP, bind irreversibly to nitrocellulose membranes.
179  MCF7 human breast cancers were spotted onto nitrocellulose microarrays and hybridized with mouse and
180 expressed proteins are printed directly onto nitrocellulose microarrays without purification.
181                       Nitroglycerin (NG) and nitrocellulose (NC) are constituents of double-base prop
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
184 roteins that have been electroblotted onto a nitrocellulose (NC) membrane.
185  specimens were processed by applying liquid nitrocellulose on exposed surfaces.
186 g to PDE5 was retained when filtered through nitrocellulose or glass-fiber membranes.
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
189 each sample are arrayed onto glass-supported nitrocellulose pads.
190 me (2 mul) of protein solution is applied to nitrocellulose paper in a grid array and dried.
191  to characterise the fluid flow of different nitrocellulose paper strips after oxygen-plasma treatmen
192 ing of colloidal gold to proteins adhered to nitrocellulose paper.
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
196        The method involves the production of nitrocellulose replica filter lifts from a plasmid cDNA
197                                              Nitrocellulose sequesters proteins and bound ligand at t
198 idylglycerol, or cardiolipin) are blotted on nitrocellulose sheets (Eastern blot) prior to transfer o
199 ver 1,000 samples may be printed on a single nitrocellulose slide.
200 us and doughnut-like on the FAST and Unisart nitrocellulose slides, whereas a better spot morphology
201 icroarray immunoassay was performed on these nitrocellulose slides.
202 behavior of a liquid droplet on and in these nitrocellulose slides.
203                      A simple plastic-backed nitrocellulose strip is the basis for an assay for detec
204 mes and the test sample and a plastic-backed nitrocellulose strip with a measurement zone were used i
205                                       On the nitrocellulose strip, antisense-reporter probes are immo
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
208 th specific nucleotide probes immobilized on nitrocellulose strips.
209  antibodies immobilized in a defined zone on nitrocellulose strips.
210 ted with immobilized ribosomal P antigens on nitrocellulose strips; affinity-purified fractions were
211 ods to develop a microarray of DNA probes on nitrocellulose substrate are discussed.
212 the human immunodeficiency virus 1 system on nitrocellulose substrates illustrate the usefulness and
213 id flow dynamics of a droplet on the various nitrocellulose substrates.
214 irst separated by SDS-PAGE, transferred to a nitrocellulose support membrane, and probed with a panel
215                                We designed a nitrocellulose-surface microarray containing human cytok
216               After LDS-PAGE and transfer to nitrocellulose these proteins bind [32P]GTP in the prese
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
219 l overlay of untreated and sialidase-treated nitrocellulose transfers, respectively.
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
226                          Results showed that nitrocellulose yielded the greatest assay sensitivity re

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top