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Cloning Murine Antibody V-genes with Non-degenerate Primers and Conversion to a Recombinant Antibody Format

机译:克隆具有非简并引物的鼠抗体V基因并转化为重组抗体形式

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摘要

Monoclonal antibodies are produced in cultured hybridoma cell lines, but these cells tend to be unstable; it is therefore necessary to rescue the corresponding genetic information. Here we describe an improved method for the amplification of antibody variable gene (V-gene) information from murine hybridoma cells using a panel of specific, non-degenerate primers. This primer set allows sequences to be rescued from all murine V-genes, except the lambda light chain genes, which rarely contribute to murine immune diversity. We tested the primers against a range of antibodies and recovered specific amplification products in all cases. The heavy and light chain variable regions were subsequently joined by a two-step cloning strategy or by splice overlap extension PCR.
机译:在培养的杂交瘤细胞系中会产生单克隆抗体,但这些细胞往往不稳定。因此,有必要挽救相应的遗传信息。在这里,我们描述了一种使用一组特定的非简并引物从鼠杂交瘤细胞扩增抗体可变基因(V基因)信息的改进方法。该引物组可从所有鼠类V基因中拯救出序列,但λ轻链基因除外,该基因很少有助于鼠类免疫多样性。我们在所有情况下都针对一系列抗体测试了引物,并回收了特异性扩增产物。随后通过两步克隆策略或通过剪接重叠延伸PCR连接重链和轻链可变区。

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