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王王世尧

新虫 (初入文坛)

[求助] LR反应假阳性过多

由于我的入门载体pentr/d/topo和目的载体1305.2的抗性都为kana抗性 根据网上的经验用pvuI单酶切入门载体 线性化 用塞默飞公司的lr反应酶 转化后涂板 用attb1和attb2特异引物菌p 条带都有 但是通过测序结果 以及之后提的质粒发现 目的基因还都是在入门载体上 求助各位大佬怎么解决

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