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1 y by fixation with paraformaldehyde, but not glutaraldehyde.
2 ttenuated when the enzyme is cross-linked by glutaraldehyde.
3 re were varied or when EDC was replaced with glutaraldehyde.
4 ent using (3-aminopropyl)triethoxysilane and glutaraldehyde.
5 d fixed with diluted paraformaldehyde and no glutaraldehyde.
6 choline oxidase (ChO) by their reaction with glutaraldehyde.
7 e loading) and tethering to the surface with glutaraldehyde.
8 r efficient interparticle cross-linking with glutaraldehyde.
9 other had Nafion with BSA cross-linked with glutaraldehyde.
10 istant than Deltager3 spores to Betadine and glutaraldehyde.
11 bon fiber electrode by cross-linking with 5% glutaraldehyde.
12 protein after it had been cross-linked with glutaraldehyde.
13 bilized with Taxol and chemically fixed with glutaraldehyde.
14 s-reactivity with GABA, arginine, lysine, or glutaraldehyde.
15 yer using cross-linking of the proteins with glutaraldehyde.
16 xposed to water, acetone, alcohol, HEMA, and glutaraldehyde.
17 cross-liking with bovine serum albumin using glutaraldehyde.
18 of 3-aminopropyltriethoxysilane (APTES) and glutaraldehyde.
19 FP pair (Ab2) via amine-amine coupling using glutaraldehyde.
20 paste electrode (MCPE) by cross-linking with glutaraldehyde.
21 sted by chemical cross-linkage analysis with glutaraldehyde.
22 chemically cross-linked PF4 tetramers using glutaraldehyde.
23 ised controlled pore glass (CPG) beads using glutaraldehyde.
25 ha-amino acids 10a-d, similarly reacted with glutaraldehyde (20) and benzotriazole to generate 5-benz
29 ent enzyme immobilization methods, including glutaraldehyde, a conventional cross-linker, and poly(et
32 clic adenosine monophosphate (bromo-cAMP) or glutaraldehyde, agents that respectively inhibit actin-m
34 een lysine residues of the folded monomer by glutaraldehyde also does not perturb the compact conform
36 the reprocessing of cellulose dialyzers with glutaraldehyde and bleach does not affect indices of blo
37 in 37 patients on chronic hemodialysis with glutaraldehyde and bleach-reprocessed cellulose dialyzer
38 erent cross-linking agents, namely, genipin, glutaraldehyde and caffeic acid, at different concentrat
40 proteins was demonstrated in the presence of glutaraldehyde and EDC/NHS (N-(3-dimethylaminopropyl)-N
42 that is significantly more resistant to both glutaraldehyde and formaldehyde than the wild-type enzym
43 BS3 and sulfo-SMPB, respectively, as well as glutaraldehyde and found no preferential dimer formation
46 nal groups were used: malondialdehyde (MDA), glutaraldehyde and hexamethylene diisocyanate (HMDC).
47 tolerance against the typically used biocide glutaraldehyde and increased susceptibility to the oxida
48 dified with chitosan and functionalized with glutaraldehyde and lactate dehydrogenase enzyme was immo
49 otocol was developed including fixation with glutaraldehyde and matrix coating with a pneumatic spray
50 as examined using the chemical cross-linkers glutaraldehyde and N-ethyl-1-3-[3-(dimethylamino)propyl]
52 mple was then taken, prior to perfusion with glutaraldehyde and removal of the sciatic nerves and cau
54 of cysteamine followed by cross-linking with glutaraldehyde and subsequent binding of 3-aminophenylbo
55 as stabilized by chemical cross-linking with glutaraldehyde and the capture ability of immuno-affinit
57 ell surface cholesterol (namely, exposure to glutaraldehyde and to low-ionic-strength buffer) also br
58 on the graphene surface were activated using glutaraldehyde and used for the covalent immobilization
59 n was impeded in the presence of the biocide glutaraldehyde and was completely inhibited by salt at c
62 rotein dimer generated by cross-linking with glutaraldehyde, and its increase in size by a hemaggluti
63 concentrations of formaldehyde and alkaline glutaraldehyde, and other commonly used disinfectants.
64 measured by quantitative cross-linking with glutaraldehyde, and the activation of the protein tyrosi
65 y native electrophoresis, cross-linking with glutaraldehyde, and unfolding data from circular dichroi
66 ssus, showed various susceptibilities to the glutaraldehyde- and isothiazolone-based test biocides.
69 ture, inhibitors of oxidative metabolism and glutaraldehyde) are substantially different for neural r
72 lization of the glucose oxidase enzyme using glutaraldehyde as crosslinking agent, producing a very e
73 bilization of human IgG on polyaniline using glutaraldehyde as the cross-linker is described in this
75 ing effect of the gold-standard cross-linker glutaraldehyde at comparable experimental conditions was
76 10-fold lower than the levels detected with glutaraldehyde-based biosensors (e.g., 1.2 muM vs 16 muM
78 re readily prepared from succindialdehyde or glutaraldehyde, benzotriazole, and N-phenylethylenediami
81 bers using covalent immobilization via amine-glutaraldehyde chemistry and inactivated S. typhimurium
83 teins to activated carboxylic acid (COOH) or glutaraldehyde (COH) groups functionalized on synthetic
84 omer cross-linking as a function of time and glutaraldehyde concentration was characterized using pol
85 functionalized magnetic nanoparticle by 60mM glutaraldehyde concentration with 10h cross-linking time
89 ovalent crosslinking of surface lysines with glutaraldehyde confirmed that wild-type and R91L protein
91 ) activated nitrocellulose (NC) membrane via glutaraldehyde coupling with 32.22% retention of initial
94 hyde-derivatized monomer (mono-glxrHb) and a glutaraldehyde cross-linked polymer (poly-glxrHb), and e
95 pectra for both purified type I collagen and glutaraldehyde cross-linked porcine aortic leaflets.
97 vestigations studied ethanol pretreatment of glutaraldehyde cross-linked porcine aortic valves as a n
98 osthetic heart valves fabricated from either glutaraldehyde cross-linked porcine aortic valves or bov
102 in vivo homotrimerization of NF7 by using a glutaraldehyde cross-linking assay, and we further showe
106 mediate of P61A FIS was further confirmed by glutaraldehyde cross-linking experiments at 95 degrees C
108 duplex or single-stranded DNA and ATPgammaS, glutaraldehyde cross-linking generated a species that be
110 of glutathione-agarose affinity binding and glutaraldehyde cross-linking indicate that ParE' exists
111 , velocity sedimentation centrifugation, and glutaraldehyde cross-linking indicated that e55K is a di
114 s well as analytical ultracentrifugation and glutaraldehyde cross-linking were utilized to evaluate t
115 this study, complementary methods including glutaraldehyde cross-linking, size-exclusion chromatogra
119 n (Ca(2+) = 89.06 +/- 17.93 microgram/mg for glutaraldehyde crosslinked elastin versus Ca(2+) = 89.73
121 -day rat subdermal implants, irrespective of glutaraldehyde crosslinking (Ca(2+) = 0.73-2.15 microgra
122 ensiformis) were prepared by desolvation and glutaraldehyde crosslinking and functionalized by cystea
123 (iii) dimerize and oligomerize, as judged by glutaraldehyde crosslinking and HPLC size chromatography
126 time course of calcification, the effect of glutaraldehyde crosslinking on calcification, and mechan
127 pe DnaK protein using either an ELISA assay, glutaraldehyde crosslinking or HPLC size chromatography.
129 the cross-linking reaction were isolated, a glutaraldehyde-derivatized monomer (mono-glxrHb) and a g
133 r AGB signals were trapped with conventional glutaraldehyde fixation and were detected by probing reg
134 -type littermates were processed by using 2% glutaraldehyde fixation for light and transmission elect
138 8-GFP:MT collision complexes were trapped by glutaraldehyde fixation, the preference for binding to p
140 and the eyes were enucleated, immersed in 2% glutaraldehyde fixative, and prepared for light and tran
147 enii inhibited the adherence of gonococci to glutaraldehyde-fixed epithelial cells like it inhibited
148 r present studies showed that the ability of glutaraldehyde-fixed eucaryotic cells to convert gonococ
151 smission electron microscopic examination of glutaraldehyde-fixed medium-sized bronchi from acute Kaw
152 ort kinesin motility, a dilute suspension of glutaraldehyde-fixed microtubules in buffer supported ki
154 riences with second-generation stent-mounted glutaraldehyde-fixed pericardial aortic valve prostheses
159 in neuroglia, whereas immunocytochemistry of glutaraldehyde-fixed tissue reveals GSH also in neurons.
160 ted strongly with poly-L-lysine-immobilized, glutaraldehyde-fixed, intact HUVEC in ELISA assays.
162 e freezing, typically comprising fixation in glutaraldehyde followed by cryoprotection with glycerol.
163 s result was confirmed by cross-linking with glutaraldehyde followed by matrix-assisted laser desorpt
164 intact mouse sperm were briefly fixed in 1% glutaraldehyde for binding studies using a standard filt
165 ase to eliminate alpha-gal epitopes and with glutaraldehyde for moderate cross-linking of collagen fi
166 ectrodes were prepared, after fixation in 3% glutaraldehyde, for SEM (n = 9) or TEM (n = 10), or both
167 ace of a poly-Si nanowire device followed by glutaraldehyde functionalization, and the PSA antibodies
168 r a period of 6 months, it cross-linked with glutaraldehyde, further lowering the biocide's aqueous c
169 covalent surface biofunctionalization route, glutaraldehyde (GA) and N-(3-dimethylaminopropyl)-N'-eth
171 lently attached onto the nanocomposite using glutaraldehyde (GA) as the linking agent, a 32-mer adeno
172 d on those surfaces after incorporation with glutaraldehyde (GA) to obtain aldehyde layers of APTES-G
173 discovered when APTMS was cross-linked with glutaraldehyde (GA), the resulting complex (APTMS-GA) di
177 )-chitosan (Chi)-lipase mixture into CaCl(2)-glutaraldehyde (GAL) solution to obtain Ca-Alg/Chi(CRL/P
178 soluble Env can be stably cross-linked with glutaraldehyde (GLA) without global modification of anti
179 zation of horse radish peroxidase (HRP), via glutaraldehyde (Glu), for deferiprone detection using im
182 led carbon nanotubes (MWCNT), chitosan (CS), glutaraldehyde (GTA) and DNA nanostructures (nsDNA).
185 rotein keyhole limpet hemocyanin (KLH) using glutaraldehyde has shown promising results in early clin
189 pore resistance to dry heat, dessication, or glutaraldehyde; (ii) an elevated core water content is a
191 that the fixation of blotted membranes with glutaraldehyde improves immunodetection of low-molecular
192 nd submerged in fresh 4% paraformaldehyde/2% glutaraldehyde in 0.1 M phosphate buffer, pH 7.4, at 4 d
194 to be an excellent alternative to the use of glutaraldehyde in chitosan crosslinking applications.
196 o describing the complexity of using KLH and glutaraldehyde in the development of vaccines to carbohy
198 ntermolecular crosslinks upon treatment with glutaraldehyde in the presence of DNA, whereas proteins
205 ted by rHb1.1 is significantly attenuated by glutaraldehyde modification of the hemoglobin monomer an
206 nzyme was selected to either accept or avoid glutaraldehyde modifications that would normally have in
207 ereas covalent attachment of BSA-Ac to APTES/glutaraldehyde-modified silica enhances the accessibilit
208 e performed intersubunit cross-linking using glutaraldehyde of the OCP and PBS followed by liquid chr
209 ffects of ConA, disuccinimidyl suberate, and glutaraldehyde on the parental enzymes and the chimera i
211 e that treating BG505 SOSIP.664 trimers with glutaraldehyde or a heterobifunctional cross-linker intr
213 hitosan gels were prepared, crosslinked with glutaraldehyde or genipin and characterized by their tex
214 were preserved by in vivo perfusion with 1% glutaraldehyde or paraformaldehyde-picric acid fixatives
217 rneal stiffening was induced in one eye with glutaraldehyde/phosphate buffered saline (PBS) immersion
218 he hemoglobin monomer and that the effect of glutaraldehyde polymerization is likely due to surface m
219 ids to nonoxidized mannan (PM) compared with glutaraldehyde-polymerized allergoids (P) or native gras
220 was to determine whether combined therapy of glutaraldehyde-polymerized bovine hemoglobin (HBOC) with
222 murine tetrameric hemoglobin (0.48 g/kg) or glutaraldehyde-polymerized bovine hemoglobin (HBOC-201,
224 dendritic cells (DCs) generated by coupling glutaraldehyde-polymerized grass pollen allergoids to no
227 ts were used; and in 1 patient, a section of glutaraldehyde-preserved allograft pericardium was used.
228 p underwent implantation of a new stentless, glutaraldehyde-preserved porcine mitral valve (Physiolog
229 ated complete inhibition of calcification of glutaraldehyde-pretreated porcine bioprosthetic aortic v
232 responses in many patients, possibly because glutaraldehyde reacts with lysine, cysteine, tyrosine, a
233 alpha(-) beta(-) strains also exhibited less glutaraldehyde resistance and slower outgrowth than did
235 Exposure of Rns to the chemical cross-linker glutaraldehyde revealed that the full-length protein is
236 nitrocellulose membranes, cross-linked with glutaraldehyde, rinsed in NaOH, restained with Ponceau S
237 ehyde (RR,1.03, 95% CI, 0.96-1.10; P=.45) or glutaraldehyde (RR, 1.13, 95% CI, 0.95-1.35, P=.18) and
238 hyde (RR=1.06, 95% CI, 0.98-1.15; P=.12), or glutaraldehyde (RR=1.09, 95% CI, 0.71-1.67; P=.70) and s
243 This may be explained by radioactive ((3)H) glutaraldehyde studies showing very low reactivity betwe
245 s possible to immobilize it on PVDF by using glutaraldehyde to conjugate the peptide to a larger, unl
246 the cross-linking of the enzyme laccase with glutaraldehyde to construct a voltammperometric biosenso
249 ne groups, which were further activated with glutaraldehyde to introduce a layer of aldehyde groups.
250 ymerization temperature (4-37 degrees C) and glutaraldehyde to manipulate collagen hydrogel fiber dia
253 were as follows: 84.1 degrees C and 0.48 for glutaraldehyde treated fibres, 74.1 degrees C and 0.59 f
255 Concomitant increases in Ca2+ and Pi in glutaraldehyde-treated cells appear to underlie the mech
257 Ca2+ and Pi concentrations were assessed in glutaraldehyde-treated porcine aortic valve fibroblasts,
260 e stiffening vs. 19.1 +/- 2.6 mm Hg after 1% glutaraldehyde treatment and 24.3 +/- 1.9 mm Hg after 4%
261 de treatment and 24.3 +/- 1.9 mm Hg after 4% glutaraldehyde treatment at 200 microL infusion; P < 0.0
262 mice immunized with GXM-TT, indicating that glutaraldehyde treatment of KLH reveals an epitope(s) th
268 thermore, MotA monomers were cross-linked by glutaraldehyde under conditions where slower complexes e
269 cross-linking experiments of HS-HoloFt with glutaraldehyde, unexpectedly, showed the complete releas
270 ide selected was covalently polymerized with glutaraldehyde until it reached a high beta-sheet second
272 as accomplished by exposing the thin film to glutaraldehyde vapors, inducing linkage formation betwee
274 ossible reaction between PAni thin films and glutaraldehyde was explored using FT-IR characterization
275 n adhesion capabilities to PS surfaces, then glutaraldehyde was used to conjugate IgGs, serving as pr
276 ized with 11-amino-1-undecanethiol, and then glutaraldehyde was used to covalently attach nitrostrept
277 ) in the absence and presence of the biocide glutaraldehyde were investigated under a range of redox
278 rcumvent this problem, low concentrations of glutaraldehyde were used to crosslink the linker histone
279 and in freestanding, for-profit units using glutaraldehyde, which accounted for <5% of all units.
280 bovine serum albumin (BSA) cross-linked with glutaraldehyde while the other had Nafion with BSA cross
281 hat polymerization of hemoglobin, rHb1.1, by glutaraldehyde would attenuate the hypertensive response
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