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Characterization of recombinant IgA producing CHO cell lines by qPCR

机译:通过qPCR表征产生IgA的重组CHO细胞系

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Immunoglobulin A (IgA) mediates a key role in mucosal immunity and is a promising novel immunotherapeutic candidate. However, difficulties in obtaining enough material often hamper in vivo explorations. We have previously generated recombinant Chinese hamster ovary (CHO) cell lines which expressed two different HIV-1 antibodies, 3D6 and 4B3, as IgA1 [ 1 ]. One cell line (3D6-IgA) shows high production rates, whereas the other (4B3-IgA) secretes rather low amounts of product. In order to unravel the mystery of productivity bottlenecks we extensively characterized the cell lines regarding growth rate, IgA productivity in long-term culture, immunofluorescence microscopy, flow cytometry and Western blotting of intra- and extracellular product (data not shown). The generated data encouraged us to analyze whether the observed antibody productivities could be explained by gene copy number (GCN) or mRNA levels.
机译:免疫球蛋白A(IgA)在粘膜免疫中起关键作用,是一种有前途的新型免疫治疗候选物。然而,获得足够材料的困难常常阻碍了体内探索。我们以前已经产生了重组中国仓鼠卵巢(CHO)细胞系,该细胞系表达两种不同的HIV-1抗体3D6和4B3作为IgA1 [1]。一种细胞系(3D6-IgA)显示出较高的生产率,而另一种细胞系(4B3-IgA)则分泌相当少量的产物。为了揭示生产力瓶颈的奥秘,我们针对细胞系的生长速度,长期培养中的IgA生产力,免疫荧光显微镜检查,流式细胞术和细胞内和细胞外产物的蛋白质印迹进行了广泛表征(数据未显示)。生成的数据鼓励我们分析观察到的抗体生产率是否可以通过基因拷贝数(GCN)或mRNA水平来解释。

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