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1 -hydroxylamine, alpha-chloroacetaldehyde and glutaraldehyde.
2 of 4-ATP and further functionalization with glutaraldehyde.
3 y by fixation with paraformaldehyde, but not glutaraldehyde.
4 ttenuated when the enzyme is cross-linked by glutaraldehyde.
5 re were varied or when EDC was replaced with glutaraldehyde.
6 ent using (3-aminopropyl)triethoxysilane and glutaraldehyde.
7 d fixed with diluted paraformaldehyde and no glutaraldehyde.
8 choline oxidase (ChO) by their reaction with glutaraldehyde.
9 e loading) and tethering to the surface with glutaraldehyde.
10 other had Nafion with BSA cross-linked with glutaraldehyde.
11 istant than Deltager3 spores to Betadine and glutaraldehyde.
12 bon fiber electrode by cross-linking with 5% glutaraldehyde.
13 protein after it had been cross-linked with glutaraldehyde.
14 bilized with Taxol and chemically fixed with glutaraldehyde.
15 s-reactivity with GABA, arginine, lysine, or glutaraldehyde.
16 yer using cross-linking of the proteins with glutaraldehyde.
17 xposed to water, acetone, alcohol, HEMA, and glutaraldehyde.
18 r efficient interparticle cross-linking with glutaraldehyde.
19 of 3-aminopropyltriethoxysilane (APTES) and glutaraldehyde.
20 FP pair (Ab2) via amine-amine coupling using glutaraldehyde.
21 paste electrode (MCPE) by cross-linking with glutaraldehyde.
22 two poorly characterized reagents: EMCS and glutaraldehyde.
23 sted by chemical cross-linkage analysis with glutaraldehyde.
24 chemically cross-linked PF4 tetramers using glutaraldehyde.
25 ised controlled pore glass (CPG) beads using glutaraldehyde.
28 ha-amino acids 10a-d, similarly reacted with glutaraldehyde (20) and benzotriazole to generate 5-benz
29 (+/-6.1)]; poly(EDMA-co-GMA)-Ethylenediamine-Glutaraldehyde [255.4 degrees C (+/-2.7)]; and aptamer-m
33 ent enzyme immobilization methods, including glutaraldehyde, a conventional cross-linker, and poly(et
36 clic adenosine monophosphate (bromo-cAMP) or glutaraldehyde, agents that respectively inhibit actin-m
38 een lysine residues of the folded monomer by glutaraldehyde also does not perturb the compact conform
40 the reprocessing of cellulose dialyzers with glutaraldehyde and bleach does not affect indices of blo
41 erent cross-linking agents, namely, genipin, glutaraldehyde and caffeic acid, at different concentrat
43 proteins was demonstrated in the presence of glutaraldehyde and EDC/NHS (N-(3-dimethylaminopropyl)-N
45 that is significantly more resistant to both glutaraldehyde and formaldehyde than the wild-type enzym
46 BS3 and sulfo-SMPB, respectively, as well as glutaraldehyde and found no preferential dimer formation
49 nal groups were used: malondialdehyde (MDA), glutaraldehyde and hexamethylene diisocyanate (HMDC).
50 oxidation/NaBH(4)-reduction sequence between glutaraldehyde and imines to generate in situ chiral 1,2
51 tolerance against the typically used biocide glutaraldehyde and increased susceptibility to the oxida
52 dified with chitosan and functionalized with glutaraldehyde and lactate dehydrogenase enzyme was immo
53 otocol was developed including fixation with glutaraldehyde and matrix coating with a pneumatic spray
54 as examined using the chemical cross-linkers glutaraldehyde and N-ethyl-1-3-[3-(dimethylamino)propyl]
56 mple was then taken, prior to perfusion with glutaraldehyde and removal of the sciatic nerves and cau
58 of cysteamine followed by cross-linking with glutaraldehyde and subsequent binding of 3-aminophenylbo
59 as stabilized by chemical cross-linking with glutaraldehyde and the capture ability of immuno-affinit
61 ell surface cholesterol (namely, exposure to glutaraldehyde and to low-ionic-strength buffer) also br
62 on the graphene surface were activated using glutaraldehyde and used for the covalent immobilization
63 n was impeded in the presence of the biocide glutaraldehyde and was completely inhibited by salt at c
66 inated self-assembled monolayer activated by glutaraldehyde, and ii) the His-tagged recombinant prote
67 rotein dimer generated by cross-linking with glutaraldehyde, and its increase in size by a hemaggluti
68 concentrations of formaldehyde and alkaline glutaraldehyde, and other commonly used disinfectants.
69 measured by quantitative cross-linking with glutaraldehyde, and the activation of the protein tyrosi
70 y native electrophoresis, cross-linking with glutaraldehyde, and unfolding data from circular dichroi
71 ssus, showed various susceptibilities to the glutaraldehyde- and isothiazolone-based test biocides.
75 ture, inhibitors of oxidative metabolism and glutaraldehyde) are substantially different for neural r
78 s modified with a synthetic peptide by using glutaraldehyde as cross-linking reagent and chitosan (CS
79 lization of the glucose oxidase enzyme using glutaraldehyde as crosslinking agent, producing a very e
80 bilization of human IgG on polyaniline using glutaraldehyde as the cross-linker is described in this
82 ing effect of the gold-standard cross-linker glutaraldehyde at comparable experimental conditions was
83 10-fold lower than the levels detected with glutaraldehyde-based biosensors (e.g., 1.2 muM vs 16 muM
85 re readily prepared from succindialdehyde or glutaraldehyde, benzotriazole, and N-phenylethylenediami
88 bers using covalent immobilization via amine-glutaraldehyde chemistry and inactivated S. typhimurium
91 teins to activated carboxylic acid (COOH) or glutaraldehyde (COH) groups functionalized on synthetic
92 omer cross-linking as a function of time and glutaraldehyde concentration was characterized using pol
93 functionalized magnetic nanoparticle by 60mM glutaraldehyde concentration with 10h cross-linking time
97 ovalent crosslinking of surface lysines with glutaraldehyde confirmed that wild-type and R91L protein
99 ) activated nitrocellulose (NC) membrane via glutaraldehyde coupling with 32.22% retention of initial
102 hyde-derivatized monomer (mono-glxrHb) and a glutaraldehyde cross-linked polymer (poly-glxrHb), and e
103 pectra for both purified type I collagen and glutaraldehyde cross-linked porcine aortic leaflets.
105 vestigations studied ethanol pretreatment of glutaraldehyde cross-linked porcine aortic valves as a n
106 osthetic heart valves fabricated from either glutaraldehyde cross-linked porcine aortic valves or bov
110 in vivo homotrimerization of NF7 by using a glutaraldehyde cross-linking assay, and we further showe
114 mediate of P61A FIS was further confirmed by glutaraldehyde cross-linking experiments at 95 degrees C
116 duplex or single-stranded DNA and ATPgammaS, glutaraldehyde cross-linking generated a species that be
118 of glutathione-agarose affinity binding and glutaraldehyde cross-linking indicate that ParE' exists
119 , velocity sedimentation centrifugation, and glutaraldehyde cross-linking indicated that e55K is a di
123 s well as analytical ultracentrifugation and glutaraldehyde cross-linking were utilized to evaluate t
124 this study, complementary methods including glutaraldehyde cross-linking, size-exclusion chromatogra
127 sensing system that combines self-assembled glutaraldehyde-cross-linked double-layered polyethylenim
129 n (Ca(2+) = 89.06 +/- 17.93 microgram/mg for glutaraldehyde crosslinked elastin versus Ca(2+) = 89.73
131 -day rat subdermal implants, irrespective of glutaraldehyde crosslinking (Ca(2+) = 0.73-2.15 microgra
132 ensiformis) were prepared by desolvation and glutaraldehyde crosslinking and functionalized by cystea
133 (iii) dimerize and oligomerize, as judged by glutaraldehyde crosslinking and HPLC size chromatography
136 time course of calcification, the effect of glutaraldehyde crosslinking on calcification, and mechan
137 pe DnaK protein using either an ELISA assay, glutaraldehyde crosslinking or HPLC size chromatography.
139 the cross-linking reaction were isolated, a glutaraldehyde-derivatized monomer (mono-glxrHb) and a g
144 r AGB signals were trapped with conventional glutaraldehyde fixation and were detected by probing reg
145 -type littermates were processed by using 2% glutaraldehyde fixation for light and transmission elect
149 8-GFP:MT collision complexes were trapped by glutaraldehyde fixation, the preference for binding to p
151 and the eyes were enucleated, immersed in 2% glutaraldehyde fixative, and prepared for light and tran
158 enii inhibited the adherence of gonococci to glutaraldehyde-fixed epithelial cells like it inhibited
159 r present studies showed that the ability of glutaraldehyde-fixed eucaryotic cells to convert gonococ
162 smission electron microscopic examination of glutaraldehyde-fixed medium-sized bronchi from acute Kaw
163 ort kinesin motility, a dilute suspension of glutaraldehyde-fixed microtubules in buffer supported ki
165 riences with second-generation stent-mounted glutaraldehyde-fixed pericardial aortic valve prostheses
170 in neuroglia, whereas immunocytochemistry of glutaraldehyde-fixed tissue reveals GSH also in neurons.
171 ted strongly with poly-L-lysine-immobilized, glutaraldehyde-fixed, intact HUVEC in ELISA assays.
173 e freezing, typically comprising fixation in glutaraldehyde followed by cryoprotection with glycerol.
174 s result was confirmed by cross-linking with glutaraldehyde followed by matrix-assisted laser desorpt
175 intact mouse sperm were briefly fixed in 1% glutaraldehyde for binding studies using a standard filt
176 ase to eliminate alpha-gal epitopes and with glutaraldehyde for moderate cross-linking of collagen fi
177 ectrodes were prepared, after fixation in 3% glutaraldehyde, for SEM (n = 9) or TEM (n = 10), or both
178 ace of a poly-Si nanowire device followed by glutaraldehyde functionalization, and the PSA antibodies
179 r a period of 6 months, it cross-linked with glutaraldehyde, further lowering the biocide's aqueous c
180 n two ways: (i) using a crosslinking agent - glutaraldehyde (GA) and (ii) by formation of the amide b
181 covalent surface biofunctionalization route, glutaraldehyde (GA) and N-(3-dimethylaminopropyl)-N'-eth
184 lently attached onto the nanocomposite using glutaraldehyde (GA) as the linking agent, a 32-mer adeno
185 y (CAb) was immobilized by crosslinking with glutaraldehyde (GA) on the amino groups of the 3D-Au-PAM
186 d on those surfaces after incorporation with glutaraldehyde (GA) to obtain aldehyde layers of APTES-G
187 BP) that was cross-linked with 0.2% and 0.6% glutaraldehyde (GA), and further calcified in vitro to s
188 discovered when APTMS was cross-linked with glutaraldehyde (GA), the resulting complex (APTMS-GA) di
192 )-chitosan (Chi)-lipase mixture into CaCl(2)-glutaraldehyde (GAL) solution to obtain Ca-Alg/Chi(CRL/P
193 soluble Env can be stably cross-linked with glutaraldehyde (GLA) without global modification of anti
194 zation of horse radish peroxidase (HRP), via glutaraldehyde (Glu), for deferiprone detection using im
197 led carbon nanotubes (MWCNT), chitosan (CS), glutaraldehyde (GTA) and DNA nanostructures (nsDNA).
200 rotein keyhole limpet hemocyanin (KLH) using glutaraldehyde has shown promising results in early clin
204 pore resistance to dry heat, dessication, or glutaraldehyde; (ii) an elevated core water content is a
206 that the fixation of blotted membranes with glutaraldehyde improves immunodetection of low-molecular
207 nd submerged in fresh 4% paraformaldehyde/2% glutaraldehyde in 0.1 M phosphate buffer, pH 7.4, at 4 d
209 to be an excellent alternative to the use of glutaraldehyde in chitosan crosslinking applications.
211 o describing the complexity of using KLH and glutaraldehyde in the development of vaccines to carbohy
213 ntermolecular crosslinks upon treatment with glutaraldehyde in the presence of DNA, whereas proteins
221 ted by rHb1.1 is significantly attenuated by glutaraldehyde modification of the hemoglobin monomer an
222 nzyme was selected to either accept or avoid glutaraldehyde modifications that would normally have in
223 ereas covalent attachment of BSA-Ac to APTES/glutaraldehyde-modified silica enhances the accessibilit
224 e performed intersubunit cross-linking using glutaraldehyde of the OCP and PBS followed by liquid chr
225 ffects of ConA, disuccinimidyl suberate, and glutaraldehyde on the parental enzymes and the chimera i
227 e that treating BG505 SOSIP.664 trimers with glutaraldehyde or a heterobifunctional cross-linker intr
229 hitosan gels were prepared, crosslinked with glutaraldehyde or genipin and characterized by their tex
230 were preserved by in vivo perfusion with 1% glutaraldehyde or paraformaldehyde-picric acid fixatives
232 es were cross-linked using paraformaldehyde, glutaraldehyde or riboflavin combined with UV-A-light or
234 rneal stiffening was induced in one eye with glutaraldehyde/phosphate buffered saline (PBS) immersion
235 he hemoglobin monomer and that the effect of glutaraldehyde polymerization is likely due to surface m
236 ids to nonoxidized mannan (PM) compared with glutaraldehyde-polymerized allergoids (P) or native gras
237 was to determine whether combined therapy of glutaraldehyde-polymerized bovine hemoglobin (HBOC) with
239 murine tetrameric hemoglobin (0.48 g/kg) or glutaraldehyde-polymerized bovine hemoglobin (HBOC-201,
241 dendritic cells (DCs) generated by coupling glutaraldehyde-polymerized grass pollen allergoids to no
244 ts were used; and in 1 patient, a section of glutaraldehyde-preserved allograft pericardium was used.
245 p underwent implantation of a new stentless, glutaraldehyde-preserved porcine mitral valve (Physiolog
246 ated complete inhibition of calcification of glutaraldehyde-pretreated porcine bioprosthetic aortic v
249 responses in many patients, possibly because glutaraldehyde reacts with lysine, cysteine, tyrosine, a
250 alpha(-) beta(-) strains also exhibited less glutaraldehyde resistance and slower outgrowth than did
252 Exposure of Rns to the chemical cross-linker glutaraldehyde revealed that the full-length protein is
253 nitrocellulose membranes, cross-linked with glutaraldehyde, rinsed in NaOH, restained with Ponceau S
254 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
255 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
260 This may be explained by radioactive ((3)H) glutaraldehyde studies showing very low reactivity betwe
262 s possible to immobilize it on PVDF by using glutaraldehyde to conjugate the peptide to a larger, unl
263 the cross-linking of the enzyme laccase with glutaraldehyde to construct a voltammperometric biosenso
266 ne groups, which were further activated with glutaraldehyde to introduce a layer of aldehyde groups.
267 ymerization temperature (4-37 degrees C) and glutaraldehyde to manipulate collagen hydrogel fiber dia
268 dase to glucose isomerase activity ratio and glutaraldehyde to protein mass ratio in combi-CLEAs prod
271 were as follows: 84.1 degrees C and 0.48 for glutaraldehyde treated fibres, 74.1 degrees C and 0.59 f
273 Concomitant increases in Ca2+ and Pi in glutaraldehyde-treated cells appear to underlie the mech
275 Ca2+ and Pi concentrations were assessed in glutaraldehyde-treated porcine aortic valve fibroblasts,
278 e stiffening vs. 19.1 +/- 2.6 mm Hg after 1% glutaraldehyde treatment and 24.3 +/- 1.9 mm Hg after 4%
279 de treatment and 24.3 +/- 1.9 mm Hg after 4% glutaraldehyde treatment at 200 microL infusion; P < 0.0
280 mice immunized with GXM-TT, indicating that glutaraldehyde treatment of KLH reveals an epitope(s) th
286 thermore, MotA monomers were cross-linked by glutaraldehyde under conditions where slower complexes e
287 cross-linking experiments of HS-HoloFt with glutaraldehyde, unexpectedly, showed the complete releas
288 ide selected was covalently polymerized with glutaraldehyde until it reached a high beta-sheet second
290 as accomplished by exposing the thin film to glutaraldehyde vapors, inducing linkage formation betwee
292 ossible reaction between PAni thin films and glutaraldehyde was explored using FT-IR characterization
293 n adhesion capabilities to PS surfaces, then glutaraldehyde was used to conjugate IgGs, serving as pr
294 ized with 11-amino-1-undecanethiol, and then glutaraldehyde was used to covalently attach nitrostrept
296 ) in the absence and presence of the biocide glutaraldehyde were investigated under a range of redox
297 rcumvent this problem, low concentrations of glutaraldehyde were used to crosslink the linker histone
298 and in freestanding, for-profit units using glutaraldehyde, which accounted for <5% of all units.
299 bovine serum albumin (BSA) cross-linked with glutaraldehyde while the other had Nafion with BSA cross
300 hat polymerization of hemoglobin, rHb1.1, by glutaraldehyde would attenuate the hypertensive response