摘要
以质粒为模板,用待测寡聚DNA片段和通用测序引物进行PCR(聚合酶链式反应),PCR片段经纯化后插入到pUC-18或pUC-19的多克隆位点中,然后用通用测序引物测定重组质粒上待测寡聚DNA片段,即可清晰、正确地知道它的序列.
The sequence of a defined DNA primer can be detected easily by a method described as below. A PCR (polymerase chain reaction) was carried out with the primer to be detected and one of the M13 universal sequencing primers. The resulting PCR fragment was purified and inserted into a PUC-18 or pUC-19 at the multicloning sites. Then the sequence of the primer to be detected can be exactly known by sequencing the recombinated plasmid with a M13 universal sequencing primer.
出处
《生物化学与生物物理进展》
SCIE
CAS
CSCD
北大核心
1996年第3期284-285,共2页
Progress In Biochemistry and Biophysics