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TRACE ELEMENT OPTIMIZATION ENHANCES PERFORMANCE AND REPRODUCIBILITY OF SERUM-FREE MEDIUM

机译:痕量元素优化增强了无血清培养基的性能和再现性

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Optimizing the quantity and composition of trace elements in the AEM (Adenovirus Expression Medium) formulation, resulted in an improved version of AEM, which is a serum-free, low protein, animal-origin free medium designed for adenovirus expression applications for PER.C6~(R) and other mammalian cell types. The improved AEM formulation supports higher maximal viable cell growth than other commercially available serum-free media. Optimization of medium trace elements has been shown to support equivalent cell growth in production batches from 100 L to 1500 L. Adding a proprietary trace element mixture to lower performing lots of medium resulted in increased cell growth comparable to better performing lots also containing the mixture. Trace element optimization has been investigated in several additional Gibco~(R) serum-free media. The resulting modifications can support maximal viable cell densities 1.5 to 3-fold greater than their predecessors. For example, HEK293 cell growth is supported with peakviable cell densities in excess of 4.0 x 10~6 viable cells/mL without a lag in cell growth during subsequent passages. Investigation continues to confirm biological productivity and to eliminate recombinant protein constituents and improve biological performance.
机译:优化AEM(腺病毒表达培养基)制剂中的微量元素的数量和组成,导致AEM的改进版,这是一种无血清,低蛋白质的动物来源性免疫培养基,用于Per.C6的腺病毒表达应用〜(r)和其他哺乳动物细胞类型。改进的AEM配方支持比其他可商购的无血清介质更高的最大可活细胞生长。已经证明了培养基微量元素的优化以支持从100L至1500L的生产批次中的等效细胞生长。将专有的微量元素混合物添加到降低的性能较少的培养基中,导致与含有混合物的更好的表现相当的细胞生长增加。已经在几种额外的Gibco〜(R)无血清媒体中研究了痕量元素优化。由此产生的修改可以支持比其前辈更大的最大活细胞密度1.5至3倍。例如,HEK293细胞生长受到过量的4.0×10〜6活细胞/ mL的易燃细胞密度,在后续通道期间没有滞后的细胞生长。调查继续证实生物生产力并消除重组蛋白成分并改善生物学性能。

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