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鸡堆型艾美耳球虫特异性单抗重链可变区基因的克隆与测序
引用本文:康桂英,秦建华,任曙光.鸡堆型艾美耳球虫特异性单抗重链可变区基因的克隆与测序[J].黑龙江畜牧兽医,2006(3):11-13.
作者姓名:康桂英  秦建华  任曙光
作者单位:河北农业大学动物科技学院 河北保定071001
基金项目:河北省自然科学基金资助项目(303226)
摘    要:提取堆型艾美耳球虫子孢子杂交瘤细胞总RNA,进行RT PCR,扩增出重链可变区基因。将已扩增出的鸡堆型艾美耳球虫特异性单抗重链可变区基因片段与pMD 18T载体连接,重组载体转化于感受态细胞JM109,筛选出阳性重组子,提取阳性重组子质粒并进行测序,得到单抗重链可变区的基因序列,为单链抗体基因的构建及免疫毒素的构建奠定了基础。

关 键 词:  堆型艾美耳球虫  单抗  可变区
文章编号:1004-7034(2006)03-0011-03
收稿时间:2005-04-25
修稿时间:2005年4月25日

Cloning and nucleotide sequencing of hight chain variable genes from species- specific monoclonal antibodies against E. acervulina
KANG Gui-ying,QIN Jian-hua,Ren Shu-guang.Cloning and nucleotide sequencing of hight chain variable genes from species- specific monoclonal antibodies against E. acervulina[J].Heilongjiang Animal Science And veterinary Medicine,2006(3):11-13.
Authors:KANG Gui-ying  QIN Jian-hua  Ren Shu-guang
Institution:College of Animal Science and Technology, Hebei Agriculture University, Baoding 071001, China
Abstract:To study the function of small molecule antibody,hight chain variable genes which was amplified from Speciesspecific Monoclonal Antibodies against E.acervulina was purified,and Cloned into clone vector pMD18T by gene recombination techniques.The recombinant plasmid was transformed into E.coli JM109.By screening,several recombinants that had been inserted with the target fragments were obtained.The positive clones containing recombination were idendified by the methods of the gene sequenceing.The result demonstrated that hight chain variable genes is 381 bp.
Keywords:Chicken  E  acervulina  monoclonal antibodies  variable genes
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