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首页> 外文期刊>Cytotechnology >Production of human-mouse chimeric antibody by high cell density perfusion culture
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Production of human-mouse chimeric antibody by high cell density perfusion culture

机译:通过高细胞密度灌注培养产生人-鼠嵌合抗体

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摘要

Two mouse myeloma cell lines which were transfected with chimeric mouse variable-human constant immunoglobulin heavy and light chain genes have been cultured at high cell density in a settling perfusion culture vessel to produce chimeric antibody specific for human common acute lymphocytic leukemia antigen (cALLA).J558L transfectant proliferated well in a serum-free medium (ITES-eRDF) to a viable cell density of 3.7×107 cells/ml and produced chimeric antibody to a maximum value of 60 μg/ml in 120 ml scale vessel. X63Ag8.653 transfectant reached a density of 1.9×107 cells/ml in 1.2 I scale vessel in serum supplemented medium (10% FCS-eRDF) and produced chimeric antibody which consisted of chimeric gamma and chimeric kappa chains to a maximum value of 5.8 μg/ml.
机译:已经在沉降灌注培养容器中以高细胞密度培养了用嵌合的小鼠可变的人恒定的免疫球蛋白重链和轻链基因转染的两种小鼠骨髓瘤细胞系,以产生对人常见的急性淋巴细胞性白血病抗原(cALLA)具有特异性的嵌合抗体。 J558L转染子在无血清培养基(ITES-eRDF)中增殖良好,达到3.7×107细胞/ ml的活细胞密度,并在120 ml规模的容器中产生最高60μg/ ml的嵌合抗体。 X63Ag8.653转染子在血清补充培养基(10%FCS-eRDF)中的1.2 I规模容器中达到1.9×107细胞/ ml的密度,并产生了由嵌合伽玛和嵌合κ链组成的嵌合抗体,最大值为5.8μg /毫升。

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