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堆形艾美球虫广东株Ea1A基因的扩增与序列测定
引用本文:吴德铭,于康震,曹永长,马静云,毕英佐. 堆形艾美球虫广东株Ea1A基因的扩增与序列测定[J]. 中国兽医科学, 2004, 34(8): 44-47
作者姓名:吴德铭  于康震  曹永长  马静云  毕英佐
作者单位:1. 华南农业大学,动物科学学院,基因工程研究室,广东,广州,510642
2. 全国畜牧兽医总站,北京,100026
摘    要:根据GenBank上登录的堆形艾美球虫Ea1A基因序列 ,设计了 1对引物 ,以抽提的广东株的总RNA为模板 ,利用反转录 聚合酶链反应 (RT PCR)扩增获得了Ea1A基因部分片段 ,并将此片段克隆至pGEM T载体中 ,经PCR、限制性内切酶分析和克隆片段序列测定、比较 ,证实了克隆片段的可靠性

关 键 词:堆形艾美球虫  Ea1A基因  RT-PCR
文章编号:1000-6419(2004)08-0044-04
修稿时间:2004-04-07

Amplification,cloning and sequencing of Ea1A gene of Eimeria acervulina isolated from Guangdong Province
WU De-ming. Amplification,cloning and sequencing of Ea1A gene of Eimeria acervulina isolated from Guangdong Province[J]. Chinese Veterinary Science, 2004, 34(8): 44-47
Authors:WU De-ming
Affiliation:WU De-ming~
Abstract:Based on Ea1A nucleotide sequence of E.acervulina published, a pair of primers were (designed). Using the total RNA of the strain Guangdong of E.acervulina, which was isolated from an outbreak in Guangdong Province, as a template, a partial segment of Ea1A was amplified by RT-PCR. The Ea1A gene fragment was cloned into pGEM-T Easy vector, and the recombinant plasmid was named pGEM-Ea1A. Finally, the plasmid was identified by PCR, restriction enzyme analysis and sequencing.
Keywords:Eimeria acervulina  Ea1A gene  RT-PCR
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