生物
寡核苷酸
聚合酶链反应
基因
低聚物限制
互补DNA
分子生物学
基因家族
克隆(编程)
遗传学
免疫球蛋白重链
基因组
计算机科学
程序设计语言
作者
James D. Marks,Michael Tristem,Abraham Karpas,Greg Winter
标识
DOI:10.1002/eji.1830210419
摘要
Abstract In recent work, the polymerase chain reaction (PCR) has been used to amplify rearranged mouse and human immunoglobulin heavy and χ light chain variable (V) genes. Here we have optimized the design of the PCR primers for human V genes and used them to amplify cDNA from human peripheral blood lymphocytes. Cloning and sequencing revealed a diverse repertoire of V genes, and the presence of members of each human V gene family. After alignment of the sequences, we identified a region conserved within V gene families, but differing between families, and used this to design family‐specific oligonucleotide probes.
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