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首页> 外文期刊>Food Control >Rapid and sensitive identification of buffalo's, cattle's and sheep's milk using species-specific PCR and PCR-RFLP techniques.
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Rapid and sensitive identification of buffalo's, cattle's and sheep's milk using species-specific PCR and PCR-RFLP techniques.

机译:使用物种特异性PCR和PCR-RFLP技术快速,灵敏地识别水牛,牛和羊奶。

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摘要

For the rapid, specific and sensitive identification of buffalo's, cattle's and sheep's milk, species-specific PCR and PCR-RFLP techniques were developed. DNA from small amount of fresh milk (100 micro L) was extracted to amplify the gene encoding species-specific repeat (SSR) region and the mitochondrial DNA segment (cytochrome-b gene). PCR amplification size of the gene encoding SSR region was 603 bp in both buffalo's and cattle's milk, while in sheep's milk was 374 bp. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique was used to discriminate between buffalo's and cattle's milk. Restriction analysis of PCR-RFLP of the mitochondrial cytochrome-b segment (359 bp) analysis showed difference between buffalo's and cattle's milk. Where, the fragment length (bp) generated by TaqI PCR-RFLP were 191 and 168, whereas no fragments were obtained in cattle's milk for cytochrome-b gene (359 bp). The proposed PCR and PCR-RFLP assays rep resent a rapid and sensitive method applicable to the detection and authentication of milk species-specific..
机译:为了快速,特异性和灵敏地鉴定水牛,牛和绵羊奶,已开发了物种特异性PCR和PCR-RFLP技术。从少量新鲜牛奶(100微升)中提取DNA,以扩增编码物种特异性重复(SSR)区和线粒体DNA片段(细胞色素b基因)的基因。在水牛和牛乳中,编码SSR区域的基因的PCR扩增大小均为603 bp,而在羊乳中为374 bp。聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术用于区分水牛和牛乳。线粒体细胞色素b片段(359 bp)分析的PCR-RFLP限制性分析显示,水牛和牛乳之间存在差异。其中,通过TaqI PCR-RFLP产生的片段长度(bp)为191和168,而在牛乳中没有获得细胞色素b基因的片段(359bp)。拟议的PCR和PCR-RFLP分析方法代表了一种快速灵敏的方法,适用于特定于牛奶种类的检测和鉴定。

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