论文部分内容阅读
根据已知的日本血吸虫菲律宾株的副肌球蛋白分子的部分cDNA序列,设计两对寡核苷酸引物(引物1/2和引物3/4),以聚合酶链式反应(PCR),用引物1/2从本室两个日本血吸虫中国大陆株cDNA库中均扩增出与预期大小(927bp)一致的特定DNA片段。巢式PCR——以第一扩增产物为模板,用引物3/4扩增出约500bp的单一条带,与预期片段(494bp)大小一致。表明PCR产物为编码副肌球蛋白的目的基因片段。
Two pairs of oligonucleotide primers (Primer 1/2 and Primer 3/4) were designed based on the partial cDNA sequence of the Paramyosin molecule of the known S. japonicum Philippine strain, using polymerase chain reaction (PCR) Primer 1/2 A DNA fragment of the same size as the expected size (927 bp) was amplified from cDNA libraries of two Chinese Schistosoma japonicum strains in our laboratory. Nested PCR - Using the first amplification product as a template, a single band of about 500 bp was amplified with primer 3/4, which was the same size as the expected fragment (494 bp). This indicates that the PCR product is a target gene fragment encoding paramyosin.