中国仓鼠卵巢细胞
克隆(编程)
胎牛血清
细胞培养
重组DNA
化学定义介质
牛血清白蛋白
细胞
单克隆抗体
分子生物学
生物
克隆(Java方法)
化学
抗体
生物化学
细胞生物学
体外
免疫学
遗传学
基因
计算机科学
程序设计语言
作者
Jiang Zhu,Jong Wei Wooh,Jeff Jia Cheng Hou,Benjamin Hughes,Peter P. Gray,Trent P. Munro
摘要
Biologic drugs, such as monoclonal antibodies, are commonly made using mammalian cells in culture. The cell lines used for manufacturing should ideally be clonal, meaning derived from a single cell, which represents a technically challenging process. Fetal bovine serum is often used to support low cell density cultures, however, from a regulatory perspective, it is preferable to avoid animal-derived components to increase process consistency and reduce the risk of contamination from adventitious agents. Chinese hamster ovary (CHO) cells are the most widely used cell line in industry and a large number of serum-free, protein-free, and fully chemically defined growth media are commercially available, although these media alone do not readily support efficient single cell cloning. In this work, we have developed a simple, fully defined, single-cell cloning media, specifically for CHO cells, using commercially available reagents. Our results show that a 1:1 mixture of CD-CHO™ and DMEM/F12 supplemented with 1.5 g/L of recombinant albumin (Albucult®) supports single cell cloning. This formulation can support recovery of single cells in 43% of cultures compared to 62% in the presence of serum.
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