摘要
为了克隆得到正确序列的蜂毒溶血肽 c DNA,对蜂毒中的蜂毒溶血肽进行了研究。实验从蜜蜂毒腺中提取总 RNA,通过 RT- PCR方法扩增得到了蜂毒溶血肽的 c DNA,扩增产物克隆到p T7Blu- T载体 ,转化大肠杆菌 JM1 0 9,DNA序列分析结果表明克隆得到的蜂毒溶血肽 c
The melittin in bee poison gland was studied to obtain the correct cDNA encoded melittin. During the experiment, the total RNA was obtained from bee poison gland and cDNA en\|coded melittin was obtained by RT PCR. After that, the obtained product was ligated to pT7Blu T vector and the recombined plasmid was transformed to the E. coli strain of JM109. The result of DNA sequence analysis demonstrated that the sequence of cDNA encoded melittin was correct.
出处
《淮海工学院学报(自然科学版)》
CAS
2002年第3期34-37,共4页
Journal of Huaihai Institute of Technology:Natural Sciences Edition
基金
南京理工大学博士后基金资助项目 (2 0 0 1-0 3 18)