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Titlebook: Eukaryotic Cell Cultures; Basics and Applicati Ronald T. Acton,J. Daniel Lynn Book 1984 The Editor(s) (if applicable) and The Author(s), un

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發(fā)表于 2025-3-21 20:06:57 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Eukaryotic Cell Cultures
副標題Basics and Applicati
編輯Ronald T. Acton,J. Daniel Lynn
視頻videohttp://file.papertrans.cn/317/316445/316445.mp4
叢書名稱Advances in Experimental Medicine and Biology
圖書封面Titlebook: Eukaryotic Cell Cultures; Basics and Applicati Ronald T. Acton,J. Daniel Lynn Book 1984 The Editor(s) (if applicable) and The Author(s), un
描述The Second International Cell Culture Congress was structured as was the First Congress to bring together scientists from academia and industry to discuss the use of cell culture in support of bioscience. It was felt that a forum whereby state-of- the-art presentations were followed by informal workshops would provide opportunity for the greatest exchange of information. Within the atmosphere of the workshop, problems common to basic as well as applied research were discussed and directions for the future were brought to light. These proceedings reflect and epitomize those discussions. Although it is difficult to cover all scientific disciplines utilizing cells in culture, we feel key areas were addressed at the Congress and are herein presented. Considerable emphasis has been given to the methods for establishing cells in culture and characterizing the cells once established as well as the improved technology for growing established cell lines. Examples of how recombinant DNA technology is being used to manipulate genes within mammalian cells, to clone mammalian genes and to insert them in prokaryotes has been included. Major emphasis has been given to the use of lymphocytes in cu
出版日期Book 1984
關(guān)鍵詞DNA; cell; cell culture; cells; endothelium; glycoprotein; interferon; leukemia; leukemia virus; molecular ge
版次1
doihttps://doi.org/10.1007/978-1-4615-9376-8
isbn_softcover978-1-4615-9378-2
isbn_ebook978-1-4615-9376-8Series ISSN 0065-2598 Series E-ISSN 2214-8019
issn_series 0065-2598
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Busines
The information of publication is updating

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Norbert H. Brockmeyer,J. K. Rockstrohcessed (from 3.9±.76 CFU-C/10. MNC to 6.7±.35 CFU-C/10. MNC). This resulted in an increase of CFU-C collected from 7.6±2.1 CFU-C/10. MNC after the first equivalent blood volume to 22.5±3.4 CFU-C/10. MNC after the third equivalent blood volume processed. These results suggest that leukapheresis and g
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Strahlenbiologie und Strahlenschutzpacked into a column, washed with 0.5M KCl and the interferon eluted with 2M KCl. The interferon was further purified by gel filtration to give an activity of approximately 10 units/mg protein. Yields were between 30–50% of the initial interferon in a volume of 25ml. Further separation of the compon
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Characteristics of Lympho-Myelopoietic Stem Cells Isolated from Canine Peripheral Bloodcessed (from 3.9±.76 CFU-C/10. MNC to 6.7±.35 CFU-C/10. MNC). This resulted in an increase of CFU-C collected from 7.6±2.1 CFU-C/10. MNC after the first equivalent blood volume to 22.5±3.4 CFU-C/10. MNC after the third equivalent blood volume processed. These results suggest that leukapheresis and g
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Mammalian Cell Culture: Technology and PhysiologyThe cost savings and product quality improvements can be enormous by approaching both the technology and physiology of mammalian cell culture from the vantage points of chemistry, thermodynamics and transport phenomena.
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