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首页> 外文期刊>Applied biochemistry and biotechnology, Part A. enzyme engineering and biotechnology >Species Identification of Fox-, Mink-, Dog-, and Rabbit-Derived Ingredients by Multiplex PCR and Real-Time PCR Assay
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Species Identification of Fox-, Mink-, Dog-, and Rabbit-Derived Ingredients by Multiplex PCR and Real-Time PCR Assay

机译:多用PCR和实时PCR测定物种鉴定狐狸,水貂,狗和兔衍生成分的鉴定

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摘要

Various detection methods have been developed to date for identification of animal species. New techniques based on PCR approach have raised the hope of developing better identification methods, which can overcome the limitations of the existing methods. PCR-based methods used the mitochondrial DNA (mtDNA) as well as nuclear DNA sequences. In this study, by targeting nuclear DNA, multiplex PCR and real-time PCR methods were developed to assist with qualitative and quantitative analysis. The multiplex PCR was found to simultaneously and effectively distinguish four species (fox, dog, mink, and rabbit) ingredients by the different sizes of electrophoretic bands: 480, 317, 220, and 209 bp. Real-time fluorescent PCR's amplification profiles and standard curves showed good quantitative measurement responses and linearity, as indicated by good repeatability and coefficient of determination R (2) 0.99. The quantitative results of quaternary DNA mixtures including mink, fox, dog, and rabbit DNA are in line with our expectations: R.D. (relative deviation) varied between 1.98 and 12.23% and R.S.D. (relative standard deviation) varied between 3.06 and 11.51%, both of which are well within the acceptance criterion of aecurrency 25%. Combining the two methods is suitable for the rapid identification and accurate quantification of fox-, dog-, mink-, and rabbit-derived ingredients in the animal products.
机译:已经开发了各种检测方法迄今为止鉴定动物物种。基于PCR方法的新技术提出了开发更好的识别方法的希望,这可以克服现有方法的局限性。基于PCR的方法使用线粒体DNA(MTDNA)以及核DNA序列。在本研究中,通过靶向核DNA,开发了多重PCR和实时PCR方法以协助定性和定量分析。发现多重PCR通过电泳带的不同尺寸同时和有效地区分四种物种(狐狸,狗,貂皮和兔)成分:480,317,220和209bp。实时荧光PCR的放大曲线和标准曲线显示出良好的定量测量响应和线性,如良好的重复性和测定系数R(2)&gt所示。 0.99。包括貂皮,狐狸,狗和兔DNA在内的季DNA混合物的定量结果符合我们的期望:R.D。(相对偏差)在1.98和12.23%之间变化,R.S.D。 (相对标准偏差)在3.06和11.51%之间变化,两者在AE& Cropency&gt的验收标准内很好。 25%。结合两种方法适用于动物产品中的狐狸,狗,水貂和兔衍生成分的快速鉴定和准确定量。

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