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Titlebook: Enzyme Engineering Volume 2; E. Kendall Pye,Lemuel B. Wingard Book 1974 Springer Science+Business Media New York 1974 Glucose.analytical c

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楼主: 浮华
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Arindam Biswas,Sukanya Koner,Jayant Singhrnative to the more usual methods of enzyme immobilization, such as entrapment inside a gel matrix or covalent attachment to an inert support, and therefore is conceptually similar to the encapsulation method of Chang, which employs solid polymer membranes. However, our method is considerably less w
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Dipankar Dasgupta,Arunava Roy,Abhijit Nagatively low cost. However, they suffer from a serious drawback in that only the terminal carboxyl and amino groups can be utilized for the covalent binding of proteins. Procedures by which the binding capacity of nylon could be increased by mild acid hydrolysis have been described recently by Hornby
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Shihua Li,Xinghuo Yu,Xiangyu Wangixing sensitive proteins having different subunits, so far it has not been possible to use it successfully for analytical or preparative purposes. Because of its hydrophilic properties, the small inter-relationships between matrix and protein, and the possibility of influencing the pore diameter by
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N. Patel,C. Edwards,S.K. Spurgeonusability, product contamination and limited reactor design, and 2) the loss of activity. The first of these problems has received considerable attention and can be circumvented by immobilization, with a wide variety of techniques, both physical and chemical in nature, having been proposed (1). On t
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https://doi.org/10.1007/978-3-319-33921-4ules (1). These include interferons, albumins and globulins. With the development of techniques for the mass culture of metazoan cells (2,3) and for macromolecule production, it seems reasonable to consider the conditions and techniques which are necessary for the culture of animal cells for enzyme production.
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https://doi.org/10.1057/9780230523371eutic value as an effective thrombolytic agent (2). Due to the low concentration of the enzyme in normal urine (3), it has been available only in small quantities, thus limiting investigators and clinicians in the study of its biochemical and physiological properties.
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Design Consideration for Animal Cell Cultures as Sources of Enzymesules (1). These include interferons, albumins and globulins. With the development of techniques for the mass culture of metazoan cells (2,3) and for macromolecule production, it seems reasonable to consider the conditions and techniques which are necessary for the culture of animal cells for enzyme production.
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