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Production of the lymphokine costimulator by activated mouse splenocytes under controlled conditions.

Bödeker Bg, Jörg Lehmann, Mühlradt Pf

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Abstract

CBA/J mouse splenocytes were induced by concanavalin A to produce the lymphokine costimulator. No serum was needed for this process. Culture conditions were optimized in a 250 ml reactor vessel. While variations of the pH or agitation by stirring had no influence, high dissolved oxygen was found to increase the yields of costimulator even at the cost of cell viability.

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What this paper is about

CBA/J mouse splenocytes were induced by concanavalin A to produce the lymphokine costimulator. No serum was needed for this process. Culture conditions were optimized in a 250 ml reactor vessel. While variations of the pH or agitation by stirring had no influence, high dissolved oxygen was found to increase the yields of costimulator even at the cost of cell viability.

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Available abstract

CBA/J mouse splenocytes were induced by concanavalin A to produce the lymphokine costimulator. No serum was needed for this process. Culture conditions were optimized in a 250 ml reactor vessel. While variations of the pH or agitation by stirring had no influence, high dissolved oxygen was found to increase the yields of costimulator even at the cost of cell viability.

Key concepts: Splenocyte, Lymphokine, Concanavalin A, Chemistry, Pellet, Interleukin 2, Cell culture, Chromatography

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Production of the lymphokine costimulator by activated mouse splenocytes under controlled conditions. — Research Paper | ScholarLens