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TA克隆及双链DNA测序:介绍一种快速克隆及分析PCR产物的方法
TA CLONING AND DOUBLE STRANDED DNA SEQUENCING:AN INTRODUCTION OF A METHOD FOR RAPID CLONING AND ANALYSlS OF PCK PRODUCTS
【摘要】 将人酸性纤维母细胞生长因子’(aFGF’)cDNA的PCR产物以TA连接方式克隆入pCR ̄(TM)II质粒,然后采用T7和Sp6启动子特异性引物对克隆的片段以双脱氧未端终止法进行双链DNA测序。结果表明这项技术是一种快捷而可靠的克隆及分析PCR产物的方法
【Abstract】 Human acidic fibroblast growth factor’cDNA amplified in PCR was cloned into pCR ̄(TM) IIplasmid by TA Iigation and sequenced directly by using dideoxynucleoside chain termination re-action primed by T7 and Sp6 primers. The results demonstrated that the technique was a rapidand relitable method for cloning and sequening PCR products.
【基金】 香港郑氏家族资助
- 【文献出处】 中国免疫学杂志 ,CHINESE JOURNAL OF IMMUNOLOGY , 编辑部邮箱 ,1994年01期
- 【分类号】Q789
- 【被引频次】24
- 【下载频次】871