摘要
目的:构建人脂联素cDNA的克隆并进行序列分析。方法:提取人脂肪组织总RNA,运用RT-PCR方法扩增人脂联素cDNA完全编码区,将扩增产物通过TA克隆技术克隆至pMD18-T载体,对重组质粒进行测序验证。结果:成功构建人脂联素cDNA的克隆,重组质粒(pMD18-T/ADPN)经测序与Genebank检索的脂联素cDNA序列进行对比证实为100%同源。结论:所构建的人脂联素cDNA克隆适于进一步的克隆表达。
Objective: To clone cDNA of human adiponectin for nucleotide sequencing. Methods: The total RNA of human adipose tissue was extracted.The cDNA complete coding region of human adiponectin was amplified by RT-PCR.The product was cloned into plasmid pMD18-Tby TA-clone.The recombinant plasmid was verified by sequencing. Results: The clone of cDNA of human adiponectin was successfully constructed.The recombinant plasmid(pMD18-T/ADPN)was verified to share 100%homologies with that of genebank by sequencing. Conclusion: The cloning of human adiponectin cDNA is adapted to further expression.
出处
《天津医药》
CAS
北大核心
2005年第2期71-73,共3页
Tianjin Medical Journal
基金
天津市教委资金资助项目(项目编号:20030325)