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Growth of Mouse L Cells in Shaken Culture and Mengovirus Plaque Formation on L Cells Suspended in Agar

机译:摇动培养中小鼠L细胞的生长和悬浮在琼脂中的L细胞上的Mengovirus斑块形成

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摘要

Procedures are described that require a minimum of equipment and maintenance for growing mouse L cells suspended in liquid medium and for plaquing mengovirus on L cells suspended in agar. Viability of L cells during storage for 1 to 2 hr at relatively high concentrations was better in media at 30 C than at 0 C, as measured by viable counts after growth for 24 hr at 35 C. The number and size of plaques increased with increasing concentration of NaHCO3 in the agar layers, but the relative difference in plaque size was maintained. Large- and small-plaque-size variants had similar virulence as determined by the rates of viability loss of L cells in liquid suspension cultures.
机译:所描述的程序仅需最少的设备和维护,即可使悬浮在液体培养基中的小鼠L细胞生长,并在悬浮于琼脂的L细胞上染上芒果病毒。 L细胞在相对较高浓度下储存1至2小时的活力在30°C的培养基中比在0°C的更好,这是通过在35°C下生长24小时后的存活数来衡量的。噬菌斑的数量和大小随增加而增加琼脂层中NaHCO 3的浓度较高,但噬菌斑大小的相对差异得以维持。大和小噬斑大小的变体具有相似的毒力,这是由液体悬浮培养物中L细胞的活力丧失速率确定的。

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