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Titlebook: Bioprocesses Including Animal Cell Culture; Conference proceedings 1988 Springer-Verlag Berlin Heidelberg 1988 DNA.Mikroorganismen.Zellku

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期刊全称Bioprocesses Including Animal Cell Culture
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学科分类Advances in Biochemical Engineering/Biotechnology
图书封面Titlebook: Bioprocesses Including Animal Cell Culture;   Conference proceedings 1988 Springer-Verlag Berlin Heidelberg 1988 DNA.Mikroorganismen.Zellku
Pindex Conference proceedings 1988
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The use of plasma protein fractions as medium supplements for animal cell culture,since the 1950s. The results however have been often confused and sometimes conflicting. Recently using very careful control of the processing conditions, especially temperature and pH, it has been found that it is possible to use Cohn fraction IV as a source of medium supplement although it appears
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,Industrial scale production of Β-interferon,l trials. In particular, the methods employed for the growth of human foreskin fibroblasts and the induction and purification of the active molecule are reviewed..The second part is dedicated to the detailed description of the only plant operating in Italy, producing clinical grade IFN. Special emph
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Strain improvement in industrial microorganisms by recombinant DNA techniques,ovement was mainly based on induced mutagenesis and only during the last few years has genetic recombination based on protoplast fusion become an additional practicable strategy..In general, recombinant DNA techniques provide an enormous potential for strain improvement in industrial microorganisms.
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Law and the Family in Ireland, 1800–1950de on down-stream purification the use of these fractions introduces new problems of possible infectious contamination which will make it essential that all cell products produced using these supplements are submitted to an effective virus inactivation procedure.
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The use of plasma protein fractions as medium supplements for animal cell culture,de on down-stream purification the use of these fractions introduces new problems of possible infectious contamination which will make it essential that all cell products produced using these supplements are submitted to an effective virus inactivation procedure.
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Gene synthesis,me other specialized methods. Their design is discussed with the implications of secondary structure as well as retrosynthetic considerations. Furthermore, considerations concerning the mutagenesis of genes as well as their mode of expression including synthetic control units are outlined.
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