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Dive into the research topics where William Biddle is active.

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Featured researches published by William Biddle.


Biotechnology Progress | 2000

Growth of NS0 Cells in Protein-Free, Chemically Defined Medium

Stephen F. Gorfien; Bill Paul; Jennifer Walowitz; Robert Keem; William Biddle; David W. Jayme

Many hybridoma and recombinant myeloma cell lines have been successfully adapted to growth in protein‐free media. Compared with serum‐supplemented media, use of protein‐free media promotes superior cell growth and protein expression and facilitates downstream purification of the expressed product. Owing to its sterol auxotrophy, the NS0 myeloma is normally grown in either a serum‐supplemented medium or a serum‐free medium supplemented with an animal‐derived lipoprotein. CD Hybridoma Medium (a protein‐free, chemically defined formulation) grows many cell lines that do not exhibit lipid dependence, but this medium does not support growth of NS0 cells without further lipid supplementation. We tested several commercially available lipid supplements in CD Hybridoma Medium, including bovine EX‐CYTE VLE. None of the tested supplements supported long‐term growth of NS0 cells in CD Hybridoma Medium. Sustained long‐term growth of NS0 cells was achieved in CD Hybridoma Medium supplemented with various animal‐ or plant‐derived lipids complexed with cyclodextrin. NS0 cells adapted to CD Hybridoma Medium supplemented with cyclodextrin‐lipid complex reached peak cell densities that were more than double those observed in serum‐supplemented medium and were cultured for more than 15 passages. These cultures were also successfully cryopreserved and recovered in this defined medium. Through the use of cyclodextrin‐based additives to CD Hybridoma Medium, it is possible to solubilize significant quantities of sterols and other lipids and to maintain a protein‐free, chemically defined cultivation environment for NS0 cells. The culture system can be kept entirely free of animal‐derived components if the supplement is made with plant‐derived or synthetic lipids.


Archive | 1998

Dry powder cells and cell culture reagents and methods of production thereof

Richard Fike; William Whitford; William Biddle


Archive | 1997

Hematopoietic cell culture nutrient supplement

John P. Daley; Barbara M. Dadey; William Biddle; Michelle G. Wysocki


Archive | 2000

Methods for reducing adventitious agents and toxins and cell culture reagents produced thereby

William Biddle; Richard M. Fike; Barbara M. Dadey; Thomas E. Bulera


Journal of hematotherapy | 1997

Animal Serum-Free Culture of Purified Human CD34+ Cells: Amplification of Progenitors from G-CSF and GM-CSF-Mobilized Peripheral Blood

Lisa R. Schain; Sonia Jain; Michelle G. Wysocki; Melinda Hall; Barbara M. Dadey; Rukmini Pennathur-Das; William Biddle; Jeffrey Wolf; Thomas B. Okarma; Jane Lebkowski


Archive | 1997

Ex Vivo Expansion of Human Hematopoietic Progenitor Cells under Serum-Free Conditions

William Biddle; Barbara M. Dadey; Michelle G. Wysocki; John P. Daley


Archive | 2010

Method for reducing extraneous factor and toxin, and cell-culturing reagent produced by the method

William Biddle; Thomas E. Bulera; Barbara M. Dadey; Richard M. Fike; バーバラ エム. ダディ,; ウイリアム シー. ビドル,; リチャード ファイク; トーマス イー. ブレラ,


Archive | 2000

Methodes de reduction des agents adventices et des toxines et reactifs pour culture de cellules ainsi produits

William Biddle; Richard M. Fike; Barbara M. Dadey; Thomas E. Bulera


Archive | 1999

Procedes servant a reduire des agents et des toxines adventices et reactifs de cultures cellulaires obtenus au moyen de ces agents et de ces toxines

William Biddle; Thomas E. Bulera; Barbara M. Dadey; Richard M. Fike


Archive | 1999

Methods for reducing adventitious agents or toxins in a sample and cell culture reagents produced thereby

William Biddle; Richard Fike; Barbara M. Dadey; Thomas E. Bulera

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