重组体用克隆位点上游和下游的T7和T3启动子序列为测序引物,用自动测序仪测序鉴定克隆的正确性。
The recombinant was sequenced by automatic sequencer with promoters T7 in upstream and T3 in downstream as sequencing primers.
采用大引物方法,利用质粒多克隆位点两侧的普通测序引物作为旁侧引物,在单个PCR管内,经2个步骤共34个循环进行定点突变。
Using normal sequencing primers adjacent to multiple clone sites of plasmid as flanking primers, a novel megaprimer method was performed in one tube with two steps and 34 cycles.
采用大引物方法,利用质粒多克隆位点两侧的普通测序引物作为旁侧引物,在单个PCR管内,经2个步骤共34个循环进行定点突变。
Using normal sequencing primers adjacent to multiple clone sites of plasmid as flanking primers, a novel megaprimer method was performed in one tube with two steps and 34 cycles.
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