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P., Henry, L., Spiros, N., and Agathos, N. (2000) Co-immobilization of manganese peroxidase from Phlebia radiata on porous silica beads. A few years later, Peters and Richards (47) showed work that supported this hypothesis because they found that, in the presence of an excess of amino groups, nucleophilic addition on the ethylenic double bond was possible. 117, No. 4, Enzyme and Microbial Technology, Vol. 11, International Journal of Biological Macromolecules, Vol. 2, Macromolecular Rapid Communications, Vol. Crosslinking characteristics and mechanical properties of a bovine pericardium fixed with a naturally occurring crosslinking agent. 183, No. The authors declare no competing interests. 94, No. 2, 2 February 2015 | Biotechnology Progress, Vol. 90, No. 119, No. 28, International Journal of Pharmaceutics, Vol. Histological staining of pre- and postsynaptic components of amphibian neuromuscular junctions. (22) did not find significant amounts of α,β-unsaturated aldehydes (structure VI) by UV-spectrophotometric analysis, which was in agreement with the findings of Hardy et al. 34, No. d 10, 29 March 2019 | European Journal of Wood and Wood Products, Vol. 69, No. Chodorov, and M.V. 166, 4 August 2017 | Journal of Nanoparticle Research, Vol. 527, No. 7, Colloids and Surfaces B: Biointerfaces, Vol. 8, No. Between 1968 and 1975, Richards and Knowles (10) and Monsan et al. Submitted. 3.3. (2004) Immobilization and kinetics of catalase onto magnesium silicate. 6-7, Journal of Molecular Catalysis B: Enzymatic, Vol. 3, Enzyme and Microbial Technology, Vol. 10, No. Their analyses by UV and IR suggested the existence of α,β-unsaturated formyl and hydroxyl groups in this molecule, and gas chromatography (GC) MS analysis indicated the molecular formula C10H14O3 (molecular weight: 182 g/mol). (52) reported the isolation of a pyridinium-type compound following the reaction of glutaraldehyde with amines and suggested this structure as a stable crosslink. Since the 1960s, glutaraldehyde has been used to couple enzyme (and protein) to carriers such as cellulosic materials (82), aminoalkylsilylated glass (83), polyacrylhydrazide (84), phenalanyl-lysine coated polystyrene beads (85), and polyethyleneimine treated magnetite (86). Hardy et al. 3. Feairheller, and E.M. Filachione, Étude du mécanisme d’établissement des liaisons glutaraldehyde protéines, Polyglutaraldehyde: a new reagent for coupling proteins to microspheres and for labeling cell-surface receptors, Synthesis and characterization of poly(glutaraldehyde). 4, 23 November 2010 | Biotechnology Progress, Vol. 42, Journal of Materials Chemistry, Vol.
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