托尔鱼甲基硫蛋白基因特异性引物的设计

Y. Atifah, Afifatul Achyar
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引用次数: 0

摘要

重金属生物标志物的使用需要在分子水平上检测和整合重金属。金属硫蛋白基因是在受到严重污染的鱼类器官中表达的基因。本研究的目的是为鱼类甲基硫蛋白寻找特异性引物。在PCR仪器中检测金属硫蛋白基因表达需要一个短链DNA序列形式的引物作为特定的靶DNA标识符。引物设计使用NCBI位点进行计算机设计,并使用genous Prime生物信息学软件进行多重比对。根据这些基因的保守区设计引物。在NCBI中使用Primer BLAST工具检查引物的特异性。结果表明,正向引物1(5′- GAT TGC GCC AAG ACT GGA ACT -3′)和反向引物1(5′- ATC ACG TTG ACC TCC TCA CTG -3′)均为扩增量为186 bp的引物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design of Specific Primer for Methallothionein Gene of Tor Fish (Tor tambra)
The use of heavy metal biomarkers is needed to detect and integrate heavy metals at the molecular level. Metallothionein gene is a gene that is expressed in fish organs that have been heavily polluted. The aim of the study was to find specific primers for methallothionein of tor fish. Detection of the metallothionein gene expression in PCR instruments requires a primer in the form of a short chain DNA sequence as a specific target DNA identifier. The primer design was performed in silico using the NCBI site and multiple-aligned using Geneious Prime bioinformatic software. Primers were designed according to the conserved region of these genes. The primers specificity was checked using Primer BLAST tools in NCBI. The results showed that the forward primer 1 (5'- GAT TGC GCC AAG ACT GGA ACT –3') and reverse primer 1 (5' – ATC ACG TTG ACC TCC TCA CTG -3') qualified as good primers with an amplicon size 186 bp.
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