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Polymerase chain reaction amplification method using a single primer which randomly anneals

机译:使用随机退火的单个引物的聚合酶链反应扩增方法

摘要

A method of amplifying template DNA by polymerase chain reaction (PCR) in which a single oligonucleotide primer having a restriction site is contacted with the template DNA, whereby the oligonucleotide randomly anneals to a single strand of the template DNA and DNA sequences complementary to the single strand are synthesized. An initial PCR amplification yields synthetic DNA sequences having the oligonucleotide sequence incorporated therein at the 5' end, and a sequence complementary to the template DNA. A second PCR amplification under higher stringency conditions amplifies regions of the template DNA to give DNA fragments having the restriction sites of the oligonucleotide primer. Thereby the method can be used to amplify trace quantities of template DNA of unknown sequence simply and efficiently, which has applications in the construction of DNA libraries of chromosome specific regions and the development of probes for chromosome mapping.
机译:一种通过聚合酶链反应(PCR)扩增模板DNA的方法,其中将具有限制性位点的单个寡核苷酸引物与模板DNA接触,从而使寡核苷酸随机退火至模板DNA的单链和与该DNA互补的DNA序列。链被合成。初始PCR扩增产生合成DNA序列,该合成DNA序列具有在5'端并入其中的寡核苷酸序列和与模板DNA互补的序列。在较高严格性条件下进行的第二次PCR扩增会扩增模板DNA的区域,以产生具有寡核苷酸引物限制位点的DNA片段。因此,该方法可用于简单,有效地扩增痕量未知序列的模板DNA,在染色体特定区域DNA文库的构建和染色体作图探针的开发中具有应用价值。

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