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利用外显子表达质粒确定秀丽隐杆线虫肌肉蛋白副肌球蛋白的抗原位点。

Antigenic sites of the muscle protein, paramyosin, in Caenorhabditis elegans determined with exon-expression plasmid.

作者信息

Kagawa H, Gengyo K

机构信息

Department of Biology, Faculty of Science, Okayama University, Japan.

出版信息

Nucleic Acids Symp Ser. 1988(19):81-4.

PMID:2465541
Abstract

Sonicated and restricted DNA fragments from plasmid clones containing the paramyosin gene, unc-15 in C. elegans were recloned into lac-z expression plasmid vectors. Numerous fragments were recovered which encoded paramyosin epitopes. These clones produced fusion protein which cross-reacted with a polyclonal and three monoclonal antibodies. The samples of sonicated fragments were also used for shot gun sequencing of the gene. Sequenced fragments were aligned with a computer analysis. Amino acid sequence of the expressed clones matched exactly to that of the exon.

摘要

来自含有秀丽隐杆线虫副肌球蛋白基因unc-15的质粒克隆的经超声处理和酶切限制的DNA片段,被重新克隆到lac-z表达质粒载体中。回收了许多编码副肌球蛋白表位的片段。这些克隆产生了与一种多克隆抗体和三种单克隆抗体发生交叉反应的融合蛋白。经超声处理的片段样本也用于该基因的鸟枪法测序。测序片段通过计算机分析进行比对。表达克隆的氨基酸序列与外显子的氨基酸序列完全匹配。

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